Abdallah Candies Recall Holiday Caramel Bites.

Abdallah Candies Announces the Voluntary Recall of Holiday Caramel Bites

Contact:
Consumer:
(952) 890-4770
FOR IMMEDIATE RELEASE – December 4, 2014 – Abdallah Candies of Burnsville, MN is taking precautionary measures and voluntarily recalling red and silver foil wrapped Holiday Caramel Bites. One customer has reported finding a peanut butter bite, wrapped in red foil, in a bag of holiday caramel bites. The date code on the bag was EK-08.
Peanut butter bites contain peanuts as an ingredient, which was not declared on the label. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
No allergic reactions or illnesses have been reported.
We believe the incident is from that code only but with an abundance of caution are recalling all the following date codes: EJ29 - EJ31and EK01- EK18. The date code can be found on the bottom left hand corner of the white label on the bottom of the cellophane bag.
This food product was distributed since Nov. 1, 2014 nationwide at gift shops and other retail locations. The product label has the SKU number 6668407116 and is sold in boxes of 6 cellophane bags with 4 red and 4 silver foil wrapped bites in each bag. The company has made the deliberate decision to recall this product to ensure the safety of their customers. The company has not been notified of any illness associated with this product.
Consumers who have purchased this product can call Abdallah Candies with their concerns. Monday through Friday 8am to 4:30 pm central time at 952-890-4770 or 800-348-7328.

Lakeland Animal Nutrition Recalls Horse Feed.

Lakeland Animal Nutrition Issues Voluntary Horse Feed Recall

Click on image for more images.

Contact:
Consumer:
863-682-4995
FOR IMMEDIATE RELEASE – December 3, 2014 – LAKELAND, Fla. – Lakeland Animal Nutrition has been informed that certain horse feeds manufactured by the company in Lakeland, Florida and distributed within the state of Florida may contain monensin and lasalocid. Serious injury or death can occur in horses consuming feeds containing monensin and/or lasalocid. Three horses reported to have consumed the feed being recalled died and other horses at the same equine facility had significant health reactions, the cause of which is still being determined. As such, please be advised that the following horse feeds are being voluntarily recalled:

• Signature Status Pellet (Lot Number 14-251) – Manufacture Date: September 8
• Signature Equilete Pellet (Lot Number 14-259) – Manufacture Date: September 16
• Signature Status Pellet (Lot Number 14-280) – Manufacture Date: October 7
• LAN 10 Pellet (Lot Number 14-281) – Manufacture Date: October 8

It is believed that all affected product has been isolated. However, if you are in possession of any of these affected products, please discontinue feeding immediately, contact your local Lakeland Animal Nutrition dealer or call 863-682-4995 and return the product(s) to your dealer for a full refund. The specific lot number can be found on the front center of the feed bag and on the feed tag.
For more information, please visit lanfeeds.com or call 863-682-4995 (Monday – Friday, 8 - 5 p.m.).

Open Nature Chile Cheese Enchiladas Recalled By Overhill Farms

Overhill Farms Voluntarily Recalls Open Nature Chile Cheese Enchiladas Sold At Safeway Stores Nationwide Due To Possible Salmonella Contamination

Contact:
Consumer:
1-323-582-9977
FOR IMMEDIATE RELEASE — December 3, 2014 — Overhill Farms, Inc. of Vernon, California is voluntarily recalling the frozen food product Open Nature Chile Cheese Enchiladas due to potential Salmonella contamination. The supplier for the organic cilantro contained in such product notified Overhill Farms that the organic cilantro may have Salmonella contamination based on routine testing conducted. The product is sold nationwide at all Safeway-owned stores, including Safeway, Carrs, Genuardi’s, Pak ‘N Save, Pavilions, Randalls, Tom Thumb and Vons.

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

No illnesses have been reported to date in connection with this voluntary recall.

Open Nature Chile Cheese Enchiladas are a frozen prepared dinner packaged in a box with a net weight of 9 oz. and marked with a UPC 0-7989310436-9. The product was sold at stores from Oct 9, 2014, through December 1, 2014.

Packages with the following lot code and “Best Before” dates are subject to the recall:

Lot Number	Best By Date
141006	AUG-06-15

The lot number and best by date can be found on the side panel of the box.
Consumers should discard this product or return it to the store for a full refund. For additional information, please call Overhill Farms, Inc. at 1-323-582-9977 (Monday – Friday, 8:30 am – 4:30 pm PST) or Safeway at 1-800-SAFEWAY.

Keystone Recalls 2015 Dutchmen Rubicon Trailers

Report Receipt Date: OCT 10, 2014
NHTSA Campaign Number: 14V640000
Component(s): FUEL SYSTEM, OTHER
Potential Number of Units Affected: 27

All Products Associated with this Recall

         Vehicle Make             Model                    Model Year(s)

• DUTCHMEN    RUBICON        2015

Details

5 Associated Documents

Manufacturer: Keystone RV Company

SUMMARY:

Keystone RV Company (Keystone) is recalling certain model year 2015 Dutchmen Rubicon trailers manufactured August 22, 2014, to September 17, 2014. The affected vehicles may have been assembled with the clamp installed incorrectly on the fuel line at the generator fuel filter and the fuel tank. As a result, the fuel line may disconnect.

CONSEQUENCE:

If the fuel line at the generator fuel filter and fuel tank disconnects, fuel may leak, increasing the risk of a fire.

REMEDY:

Keystone has notified owners, and dealers will inspect the fuel line clamp on the generator and the fuel tank and reposition it, as necessary, free of charge. The recall began on October 17, 2014. Owners may contact Keystone customer service at 1-866-425-4369. Keystone's number for this recall is 14-218.

NOTES:

Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.safercar.gov.

Honda Recalls Acura MDX and Acura RLX

Report Receipt Date: OCT 10, 2014
NHTSA Campaign Number: 14V639000
Component(s): SEAT BELTS
Potential Number of Units Affected: 43,481

All Products Associated with this Recall

        Vehicle Make     Model            Model Year(s)

• ACURA       MDX             2014-2015
• ACURA       RLX               2014

Details

8 Associated Documents

Manufacturer: Honda (American Honda Motor Co.)

SUMMARY:

American Honda Motor Company (Honda) is recalling certain model year 2014-2015 Acura MDX vehicles manufactured April 23, 2013, to August 25, 2014, and 2014 Acura RLX vehicles manufactured November 5, 2012, to November 25, 2013. In the affected vehicles, the driver and front passenger seat belt may not extend or retract in low temperatures.

CONSEQUENCE:

A seatbelt that does not function increases the risk of injury in a crash.

REMEDY:

Honda has notified owners, and dealers will replace the driver and front passenger seat belts, free of charge. The recall began in November 2014. Owners may contact Acura customer service at 1-800-382-2238. Honda's number for this recall is JK7 for the MKX, and JK8 for the RLX.

NOTES:

Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.safercar.gov.

Chrysler Recalls TOWN AND COUNTRY, GRAND CARAVAN, And WRANGLER

Report Receipt Date: OCT 08, 2014
NHTSA Campaign Number: 14V632000
Component(s): TIRES
Potential Number of Units Affected: 10,390

All Products Associated with this Recall

Vehicle MakeModelModel Year(s)

• CHRYSLER           TOWN AND COUNTRY                 2014
• DODGE                 GRAND CARAVAN                         2014
• JEEP                      WRANGLER                                     2014

Details

5 Associated Documents

Manufacturer: Chrysler Group LLC

SUMMARY:

Chrysler Group LLC (Chrysler) is recalling certain model year 2014 Chrysler Town and Country and Dodge Grand Caravan vehicles manufactured March 20, 2014, to April 22, 2014, and 2014 Jeep Wrangler vehicles manufactured March 21, 2014, to April 22, 2014. Due to a software error, the Tire Pressure Monitoring System (TPMS) may fail to learn the locations of the individual sensors while the vehicle is being driven. As a result, the low tire pressure warning light will illuminate, despite the the tire pressures being within specification. Should one of the tires lose air pressure, the driver would not be notified of the change in air pressure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard No. 138, "Tire Pressure Monitoring Systems."

CONSEQUENCE:

If the TPMS light illuminates because the sensors cannot be located, it could mask an actual low tire pressure condition, possibly resulting in tire failure, increasing the risk of a crash.

REMEDY:

Chrysler has notified owners, and dealers will reprogram the TPMS module, free of charge. The recall began on October 23, 2014. Owners may contact Chrysler customer service at 1-800-853-1403. Chrysler's number for this recall is P63.

NOTES:

Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.safercar.gov.

Heart Sync Inc. Recalls Multi-function Defibrillation Electrodes For Device Correction

Heart Sync Inc. Issues a Voluntary Device Correction for Multi-function Defibrillation Electrodes

Click on image for more images

Contact:
Consumer:
734-213-5530
FOR IMMEDIATE RELEASE — November 26, 2014 — Detroit, MI Heart Sync Inc. announces that it has notified customers of a Voluntary Urgent Device Correction for certain Multi-function Defibrillation Electrodes due to a connector compatibility issue with Philips FR3 and FRx Defibrillator Units.
These electrodes will not connect with Philips FR3 or FRx AED units. The FRx AED unit requires the pads to be pre-connected, and will issue a continuous alarm chirp to alert the user that the proper pads are not connected to the unit prior to use. The FR3, however, does not require pre-connection and the user may not discover the incompatibility issue until the AED must be used. This may result in a delay in electrical therapy, which can lead to death or serious adverse consequences.
Heart Sync has not received any complaints or Medwatch reports of injuries associated with this Voluntary Device Correction to date.
The affected multi-function electrodes were distributed globally to distributors and medical facilities from October 26, 2011 through November 26, 2014.
Heart Sync alerted customers to this issue by letter on November 11, 2014 and is in the process of revising its labeling to clarify the use of these electrodes as incompatible with the Philips FR3 and FRx AED units. There are a total of 113,750 electrodes affected by this voluntary device correction. No product needs to be returned to Heart Sync.
All lot numbers of the following Heart Sync electrodes are affected:

• Catalog Number C100-PHILIPS - Adult Radiotransparent Electrode
• Catalog Number C100AC-PHILIPS - Adult Radiotransparent Electrode
• Catalog Number T100LO-PHILIPS - Adult Radiotransparent Electrode
• Catalog Number T100-PHILIPS Radiotranslucent Electrode
• Catalog Number T100AC-PHILIPS Radiotranslucent Electrode

Philips FR3 and FRx AED units should only be used with the electrodes specified in the equipment manuals.
For further information or to report a problem, please contact Heart Sync at 734-213-5530, 24 hours a day, 7 days a week, or email at Jahana@heartsync.net.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online: www.fda.gov/medwatch/report.htm

Cargill Recalls 'Your Fresh Market' Brand Ground Beef due to E. coli O157

Advisory date: December 1, 2014

Reason for advisory: Microbiological - E. coli O157

Hazard classification: Class 1

Company / Firm: Cargill Meat Solutions (Est. 700)

Distribution: Alberta, British Columbia, Manitoba, Saskatchewan

Extent of the distribution: Consumer

 

Advisory details

Ottawa, December 1, 2014 - Cargill Meat Solutions (Est. 700) is recalling Your Fresh Market brand ground beef products from the marketplace due to possible E. coli O157 contamination.  Consumers should not consume the recalled products described below.
The following products have been sold at Walmart stores in Alberta, British Columbia, Manitoba and Saskatchewan.

Products

Brand Name	Common Name	Size	Codes(s) on Product	UPC
Your Fresh Market	Extra Lean Ground Beef Sirloin	475 g	Best Before 2014.NO.28	6 05388 18363 7
Your Fresh Market	Extra Lean Ground Beef	475 g	Best Before 2014.NO.28	6 05388 18369 9
Your Fresh Market	Medium Ground Beef	475 g	Best Before 2014.NO.28	6 05388 18365 1
Your Fresh Market	Lean Ground Beef	475 g	Best Before 2014.NO.28 and 2014.NO.29	6 05388 18376 7
Your Fresh Market	Extra Lean Ground Beef	900 g	Best Before 2014.NO.28	6 05388 18372 9
Your Fresh Market	Lean Ground Beef	900 g	Best Before 2014.NO.28	6 05388 18378 1
Your Fresh Market	Lean Ground Beef	1.6 kg	Best Before 2014.NO.28 and 2014.NO.29	6 05388 18379 8

What You Should Do

Check to see if you have recalled products in your home. Recalled products should be thrown out or returned to the store where they were purchased.
Food contaminated with E. coli O157 may not look or smell spoiled but can still make you sick. Symptoms can include nausea, vomiting, mild to severe abdominal cramps and watery to bloody diarrhea. In severe cases of illness, some people may have seizures or strokes, need blood transfusions and kidney dialysis or live with permanent kidney damage. In severe cases of illness, people may die.

• Learn more about the health risks
• Sign up for recall notifications by email or follow us on Twitter
• View our detailed explanation of the food safety investigation and recall process

Background

This recall was triggered by test results. The Canadian Food Inspection Agency (CFIA) is conducting a food safety investigation, which may lead to the recall of other products. If other high-risk products are recalled, the CFIA will notify the public through updated Food Recall Warnings.
The CFIA is verifying that industry is removing recalled product from the marketplace.

Illnesses

There have been no reported illnesses associated with the consumption of these products.

More information

Cargill Meat Solutions:  Connie Tamoto, Communications Manager, Cargill, Winnipeg, Manitoba, Canada, Office: 204-947-6187, Mobile: 204-918-0344, connie_tamoto@cargill.com
Wal-Mart Canada Corp:  Alex Roberton, Director, Corporate Affairs & Social Media, 905-821-2111 ext. 75402, alex.roberton@walmart.com
For more information, consumers and industry can contact the CFIA by filling out the online feedback form.

Packaging Photos;

 

 

 

Ford Recals 2007-2008 Lincoln MKX, and Ford Edge vehicles,

Report Receipt Date: OCT 29, 2014
NHTSA Campaign Number: 14V682000
Component(s): FUEL SYSTEM, GASOLINE
Potential Number of Units Affected: 186,024

All Products Associated with this Recall

Vehicle MakeModelModel Year(s)

• FORDEDGE2007-2008
• LINCOLNMKX2007-2008

Details

5 Associated Documents  

Name	Description	Size(KB)
RCAK-14V682-3405.pdf	Recall Acknowledgement	49
RCLRPT-14V682-4575.PDF	Defect Notice 573 Report	29
RCMN-14V682-5106.pdf	Manufacturer Notices(to Dealers,etc)	126
RCORRD-14V682-8382.pdf	Other Recall Related Documents - Chronology	12
RMISC-14V682-4252.pdf	Miscellaneous Document - Press Release	31

 

Manufacturer: Ford Motor Company

SUMMARY:

Ford Motor Company (Ford) is recalling certain model year 2007-2008 Lincoln MKX, and Ford Edge vehicles, manufactured June 15, 2006, to September 22, 2008, and originally sold, or currently registered in, Connecticut, Delaware, Illinois, Indiana, Iowa, Kentucky, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Vermont, West Virginia, Wisconsin and the District of Columbia. Due to corrosion from salt water exposure such as from road salt use, the affected vehicles may leak fuel from the fuel tank seam weld under the tank mounting reinforcement brackets.

CONSEQUENCE:

A fuel leak in the presence of an ignition source increases the risk of a fire.

REMEDY:

Ford will notify owners. The remedy is currently being developed. The recall is expected to begin on December 8, 2014. Owners may contact Ford customer service at 1-866-436-7332. Ford's number for this recall is 14S22.

NOTES:

Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.safercar.gov.

NHTSA To Determine if Graco Failed to Report Safety Defect in a Timely Manner

NHTSA Opens Investigation into Graco’s Handling of Largest Child Seat Recall in U.S. History 

NHTSA 47-14
Monday, December 1, 2014
Contact: Karen Aldana, 202-366-9550, Public.Affairs@dot.gov

Agency to Determine if Graco Failed to Report Safety Defect in a Timely Manner

WASHINGTON – The U.S. Department of Transportation's National Highway Traffic Safety Administration (NHTSA) today announced that it opened an investigation into the timeliness of Graco Children’s Products, Inc.’s (Graco) reporting of a safety defect in child seats. The defect involves buckles of child and infant car seats that stick or become stuck in the latched position, creating an unreasonable risk to a child’s life in the event of an emergency.
After continued pressure from NHTSA, Graco eventually recalled over six million defective car seats earlier this year, the largest child seat recall in U.S. history.
“The Department is committed to ensuring that parents have peace of mind knowing that the car seat in which they are placing their child and their trust is safe and reliable,” said U.S. Transportation Secretary Anthony Foxx. “Any delays by a manufacturer in meeting their obligations to report safety issues with the urgency they deserve, especially those that impact the well-being of our children, erodes that trust and is absolutely unacceptable.”
Under the National Traffic and Motor Vehicle Safety Act, once a manufacturer knows or should reasonably know that an item of motor vehicle equipment, such as a car seat, contains a safety related defect, the manufacturer has a maximum of five business days to notify the agency. NHTSA’s investigation will evaluate the facts of the case to determine if Graco violated the law.
“There is no excuse for delaying a recall to address any safety related defect,” said NHTSA Deputy Administrator David Friedman. “If Graco delayed in protecting children and infants from this defect, we will hold them accountable.”
If NHTSA’s investigation finds that Graco was untimely in reporting the defect, the manufacturer could be fined up to $35 million in civil penalties. The Administration’s four-year reauthorization bill – the GROW AMERICA Act – proposes to increase the Congressionally-established cap on fines from $35 million to $300 million. The Department of Transportation transmitted the GROW AMERICA Act to Congress in spring 2014.

• View NHTSA’s Closing Resume
• View NHTSA’s Timeliness Query Opening Resume

The Kroger Co. Recalls Private Selection Denali Extreme Moose Tracks Ice Cream

Select Containers of Private Selection Denali Extreme Moose Tracks Ice Cream Recalled for Undeclared Allergen

Contact:
Consumer:
800-KROGERS (800-576-4377)

Media:
Keith Dailey, (513) 762-1304

Investors:
Cindy Holmes, (513) 762-4969
FOR IMMEDIATE RELEASE – November 24, 2014 – CINCINNATI, OH – The Kroger Co. (NYSE: KR) said today it is recalling select containers of Private Selection Denali Extreme Moose Tracks Ice Cream sold in 13 states because it may contain peanuts not listed on the label.
Item Description:
Private Selection Denali Extreme Moose Tracks Ice Cream sold in 48-ounce containers with a "sell by" date of April 16, 2015 under the following UPC Code: 11110-00456.
Customers should return the product to stores for a full refund or replacement. No customer illnesses have been reported to date.
People who are allergic to peanuts could have a serious or life-threatening reaction if they consume this product. For consumers who are not allergic to peanuts, there is no safety issue with the product.
Store Locations
Stores in the following states are included in this recall: Bakers stores in Nebraska; Dillons stores located in Kansas and Missouri; Gerbes stores located in Missouri; Fred Meyer stores located in Alaska, Idaho, Oregon and Washington; Food 4 Less stores located in California and Nevada; King Soopers and City Market stores located in Colorado and Wyoming; Ralphs stores located in California; Smith’s stores located in Idaho, Montana, Nevada, Utah and Wyoming and QFC stores located in Oregon and Washington.
Not included in this recall are Kroger, Food 4 Less (Chicago), Fry’s stores and Smith’s stores located in Arizona and New Mexico.
Dillons, Fred Meyer, QFC, King Soopers, City Market, Ralphs, Food 4 Less (west coast), Bakers, Gerbes and Smith’s removed items from store shelves and initiated a customer recall notification system that alerts customers who may have purchased recalled Class 1 products through register receipt tape messages and phone calls.
Customers who have questions about this recall may contact Kroger toll-free at 800-KROGERS (800-576-4377). For more information, please visit www.kroger.com/recall_alerts.

Pro Armor Recalls Polaris RZR 800 and 900 Utility Vehicle Doors

Pro Armor Recalls Doors for Polaris RZR 800 and 900 Utility Vehicles Due to Impact, Laceration Hazards 

Recall Summary

Name of product: Utility vehicle doors

Hazard: The latch pin can disengage from the latch and allow the door to open while the vehicle is moving, posing a risk of ejection of an unrestrained rider and impact or laceration hazards.
 
Remedy:Repair

Consumer Contact:
Pro Armor toll-free at (888) 312-7667 between 8 a.m. and 5 p.m. PT Monday through Friday or online at www.proarmor.com and click on “2014 Latch Recall” halfway down the left side of the page for more information.

 

Goal Zero Recalls Sherpa Brand Battery Packs Due to Fire Hazard

Recall Summary

Name of product: Goal Zero Sherpa brand 50 and 120 rechargeable battery packs  
Hazard: The battery packs can overcharge, overheat, bulge and melt the battery pack’s enclosure, posing a fire hazard and risk of property damage.

Remedy: Replace

Consumer Contact:
Goal Zero toll-free at (877) 897-3193 from 6 a.m. to 6 p.m. MT Monday through Friday or online at www.goalzero.com and click on “Product Notifications” for more information.

Units

About 10,000 in the U.S. and 110 in Canada

Description

This recall involves Goal Zero’s Sherpa brand 50 and 120 rechargeable battery packs that are used to charge cell phones, tablets, laptops and other devices. The battery packs can be plugged into an A/C wall outlet, a 12 volt car charger or an attachable solar panel for recharging.  The lithium ion iron phosphate battery packs are silver and black. Goal Zero and Sherpa 50 or 120 are printed on one side of the battery pack. The serial number is printed on the other side. Serial numbers that start with S/N 11002 or S/N 11102 are included in the recall. Sherpa 50 battery packs with serial numbers starting with S50 are not included in this recall.

Incidents/Injuries

Goal Zero has received one report of a fire and two reports of property damage due to the battery packs overheating.  One consumer reported becoming ill after breathing fumes from an overheated battery pack.

Remedy

Consumers should immediately stop using the recalled battery packs and contact Goal Zero for a free replacement battery pack.

Sold at

REI and other sporting goods stores nationwide and online at Amazon.com and Goalzero.com from March 2010 through November 2013 for between $200 and $400.

Importer(s)

Goal Zero LLC, of Bluffdale, Utah

Manufactured in

China

CONMED Issues a Device Correction for PadPro and R2 Multi-function Defibrillation Electrodes

CONMED Corporation Issues a Voluntary Device Correction for PadPro and R2 Multi-function Defibrillation Electrodes

Contact:
Consumer:
727-399-5276
mutlifunctionelectrodes@conmed.com
FOR IMMEDIATE RELEASE – November 25, 2014 – Utica, New York – CONMED Corporation announces that it has notified customers of a Voluntary Urgent Device Correction for certain PadPro and R2 Multi-function Defibrillation Electrodes due to a connector compatibility issue with Philips FR3 and FRx Defibrillator Units.
These electrodes will not connect with Philips FR3 or FRx AED units. The FRx AED unit requires the pads to be pre-connected, and will issue a continuous alarm chirp to alert the user that the proper pads are not connected to the unit prior to use. The FR3, however, does not require pre-connection and the user will not discover the incompatibility issue until the AED must be used. This may result in a delay in therapy.
CONMED has not received any complaints or Medwatch reports of injuries associated with this Voluntary Device Correction.
The affected multi-function electrodes were distributed globally to distributors and medical facilities from March 1, 2012 through October 29, 2014.
CONMED alerted customers to this issue by letter on November 6, 2014 and is in the process of revising its labeling to clarify the use of these electrodes as incompatible with the Philips FR3 and FRx AED units. There are a total of 174,610 electrodes affected by this voluntary device correction. No product needs to be returned to CONMED.
All lot numbers of the following CONMED electrodes are affected:

• Catalog Number 2001H - Adult Radiotransparent Electrode
• Catalog Number 2001H-C - Adult Radiotransparent Electrode
• Catalog Number 2001H-PC - Adult Radiotransparent Electrode
• Catalog Number 2516H - Adult Radiotranslucent Electrode
• Catalog Number 2516H-PC - Adult Radiotransparent Electrode
• Catalog Number 2603H - Pediatric Radiotranslucent Electrode
• Catalog Number 2602H - Mini Pediatric Radiotranslucent Electrode
• Catalog Number 3115-1750 - Pediatric R2 Multifunction Electrode
• Catalog Number 3115-1751 - R2 Multifunction Electrode

The Food and Drug Administration has classified this as a Class 1 Recall, the most serious recall where there is a reasonable risk of serious adverse health consequences or death.
For further information or to report a problem, please contact CONMED at 727-399-5276, Monday – Friday, 8 am – 5 pm ET, or email at mutlifunctionelectrodes@conmed.com
Health care professionals and customers may report adverse events or quality problems experienced with the use of this product to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail, fax or by phone.

• Online: www.fda.gov/medwatch/report.htm
• Regular Mail: use postage-paid FDA form 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to MedWatch 5600 Fishers Lane, Rockville, MD 20852-9787
• Fax: 1-800-332-0178
• Phone: 1-800-332-1088

About CONMED
CONMED is a medical technology company with an emphasis on surgical devices and equipment for minimally invasive procedures. Headquartered in Utica, New York, the Company's 3,600 employees distribute its products worldwide with a direct selling presence in 16 countries outside the United States. International sales constitute approximately 50% of the Company's revenues.

Whole Foods Recalls Vegan Pumpkin Pie due to Undeclared Walnuts

Whole Foods Market’s Southwest Region recalls Vegan Pumpkin Pie due to Undeclared Walnuts

Contact:
Consumer:
www.wholefoodsmarket.com
Media:
Kate Neu, Whole Foods Market
Kate.neu@wholefoods.com

FOR IMMEDIATE RELEASE — November 26, 2014 — Austin, TX — Whole Foods Market is recalling “Vegan pumpkin pie” produced and sold in the Southwest Region, which includes TX, OK, LA, AR, due to undeclared walnuts. The product was sold as half and full pies packaged in both clear, clamshell packaging and brown, Kraft paper boxes UPCs 24917100000 and 24917300000 with “sell by” dates of 10/27/14-­‐‑11/30/14. People who have an allergy or severe sensitivity to walnuts run the risk of serious or life-­‐‑threatening allergic reaction if they consume these products.

The vegan pumpkin pies contain walnuts as an ingredient, which was not declared on the label.

Signage is posted to notify customers of this recall, and all affected product has been removed from shelves.

No allergic reactions or illnesses have been reported to date.

Consumers who have purchased this product from any Whole Foods Market Southwest stores in TX, OK, LA, or AR may bring their receipt to the store for a full refund. Consumers with questions should contact their local store between the hours of 9am and 5pm CST.

Customers may find their nearest Whole Foods Market at www.wholefoodsmarket.com

Whole Foods Recalls Tarte Aux Pommes Due to Undeclared Almonds

Whole Foods Market West Hartford, Bishops Corner and Glastonbury Recall Tarte Aux Pommes Due to Undeclared Almonds

Contact:
Consumer:
617-492-5500, 9am - 5pm EST
FOR IMMEDIATE RELEASE – December 1, 2014 – CAMBRIDGE, MA – Three Connecticut Whole Foods Market locations are recalling “Tarte Aux Pommes” produced and sold in West Hartford Center, Bishops Corner and Glastonbury, Connecticut due to an undeclared almonds. The 6 inch tarte was mislabeled as a “Tarte Aux Pomme 10in” and has a “best by” date between November 20 and December 1, 2014.
The six inch tarte contained almonds as an ingredient, which was not declared on the label. People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume these products.
The tarte was sold in the stores between Sunday, November 16 and Friday, November 28, 2014.
Signage is posted to notify customers of this recall, and all affected product has been removed from shelves.
No allergic reactions or illnesses have been reported.
Consumers who have purchased this product from Whole Foods Market West Hartford Center, Bishops Corner or Glastonbury, Connecticut may bring their receipt to the store for a full refund. Consumers with questions should contact their local store or call 617-492-5500 between the hours of 9am and 5pm EST.