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This site is not intended to provide medical advice, diagnosis or treatment. RecallsGlobal - Recallr will bring you all possible listed recalls to the fore. Food Recalls, Medicine recalls, consumer product recalls, cosmetics recalls, vehicle recalls, boat recalls, Bus Recalls, Truck Recalls, Car Recals and any other recalls that affect our lives will be found and listed. Recallr Blog for Recalls Global. Sources include, FDA, USDA, CPSC, Health Canada, FSIS and Company news releases.
Wednesday, May 7, 2008
CHRYSLER RECALLS 2007-2008 JEEP WRANGLER
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| Component: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS | ||||||||||||||
| Potential Number Of Units Affected : 1585 | ||||||||||||||
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TRIPLE E RECREATIONAL VEHICLES RECALLSA391Q AND A393T MOTOR HOMES
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| Component: STEERING:LINKAGES:TIE ROD ASSEMBLY | |||||||||||||||||
| Potential Number Of Units Affected : 3 | |||||||||||||||||
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GENERAL MOTORS RECALL 2008 SATURN VUE VEHICLES
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| Component: POWER TRAIN:AUTOMATIC TRANSMISSION | ||||||||||||||
| Potential Number Of Units Affected : 26 | ||||||||||||||
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Lezza Blue Raspberry Italian Ice Recall Update.
Updated Press Release: Lezza Blue Raspberry Italian Ice Recalled
Contact:
Cedar Crest Specialties, Inc.
1-866-233-2788
FOR IMMEDIATE RELEASE -- May 6, 2008 -- Cedar Crest Specialties, Inc., Manitowoc, Wisconsin announced on Friday, May 2nd 2008 a recall on one lot code of Lezza Blue Raspberry Italian Ice because, it may contain milk allergen protein that is not listed in the product’s ingredient statement. People who have an allergy or severe sensitivity to milk may experience a potentially serious or life-threatening allergic reaction if they consume this product.
The product is in round plastic pint containers with a lot code of 2116. Blue Raspberry is the flavor of the product.
The product was distributed to retail outlets in Illinois, Wisconsin, Oklahoma, Texas, Michigan, Louisiana, Kansas, Indiana, Georgia, Florida, Ohio, Missouri, Kentucky, Nebraska, Pennsylvania, Arkansas, and Minnesota during 2006 and 2007.
There is no health risk for consumers who are not allergic to milk.
No other Lezza Italian Ice products are included in this recall. The product is flavored frozen water ice and must be kept frozen.
There is one reported allergic reaction attributed to this product. After customer reported allergic reaction, product in customer’s possession was retrieved and sent to independent lab for analysis. Unopened product was also sent to independent lab for testing. Decision for recall was reached after lab tests were completed. Only one complaint was filed about lot code 2116.
Concerned consumers are encouraged to return any affected product to the place of purchase to receive a full refund. Consumers with questions or concerns may contact Cedar Crest Specialties, Inc. at 1-866-233-2788.Blount Fine Foods recalls Blount All Natural New England Clam Chowder
Blount Fine Foods Issues Allergy Alert On Undeclared Shrimp in All Natural New England Clam Chowder, 20 Oz Cup Contact:
Blount Fine Foods
1-800-274-2526
FOR IMMEDIATE RELEASE -- May 6, 2008 -- Blount Fine Foods of Fall River, MA is recalling Blount All Natural New England Clam Chowder, Net Wt. 20 oz with Lot: 0424086D, Sell by date: 6/23/2008, because it may contain undeclared shrimp. People who have an allergy or severe sensitivity to shrimp run the risk of serious or life-threatening allergic reaction if they consume these products. Our firm has recovered 1,400 of 1,416 units produced, 16 units are in distribution.
Blount New England Clam Chowder was distributed through the following supermarket chains: Shaw's Supermarkets (in Massachusetts and Connecticut), Omni Foods (in Weston, MA), Donelan Market (in Acton and Littleton, MA), and The Cirelli Marketplace store (Middleboro, MA). The product is identified as a 20oz plastic cup with a film seal and plastic lid. The dark blue product label reads: Blount Signature Soups All Natural New England Clam Chowder, Keep Refrigerated. The lot code and sell by date are printed in black ink on the bottom of the cup.
No illnesses have been reported to date. The recall was initiated after it was discovered that product containing shrimp was distributed in packaging that did not reveal the presence of shrimp. Subsequent investigation indicates the problem was caused by an isolated, temporary breakdown in the company's production and packaging processes.
Consumers who have purchased Blount All Natural New England Clam Chowder are urged to return it to the place of purchase for a full refund. Consumers who have health-related concerns should contact their physician. Consumers with questions may contact the company at 1-800-274-2526.
Tuesday, May 6, 2008
Cedar Crest Specialties, Inc. Recalls Lezza Blue Raspberry Water Ice
Lezza Blue Raspberry Water Ice Recalled from Three Midwestern States
Contact:
Cedar Crest Specialties, Inc.
1-866-233-2788
FOR IMMEDIATE RELEASE -- May 2, 2008 -- Cedar Crest Specialties, Inc. today announced a recall on one lot code of Lezza Blue Raspberry Water Ice in round plastic pint containers with a lot code of 2116 because it may contain undeclared milk protein. The product was distributed to retail outlets in Illinois, Wisconsin, and Minnesota during 2006 and 2007.
The product is being recalled because it may contain milk allergen protein that is not listed in the product’s ingredient statement. People who have an allergy or severe sensitivity to milk may experience a potentially serious or life-threatening allergic reaction if they consume this product.
There is no health risk for consumers who are not allergic to milk.
No other Lezza water ice products are included in this recall.
There is one reported allergic reaction attributed to this product.
Concerned consumers are encouraged to return any affected product to the place of purchase to receive a full refund. Consumers with questions or concerns may contact Cedar Crest Specialties, Inc. at 1-866-233-2788.Hydrox Labs Recalls Cardinal Health labeled alcohol-free mouthwash.
Hydrox Labs Issued a Voluntary Recall of Alcohol-Free Mouthwash Nationwide Distributed by Cardinal Health
Contact:
Cardinal Health
800-292-9332
FOR IMMEDIATE RELEASE -- Elgin, IL -- May 2, 2008 Hydrox Labs, Elgin, IL has issued a voluntary recall of Cardinal Health labeled alcohol-free mouthwash. As a result of this recall, Cardinal Health is initiating a voluntary recall of the same alcohol-free mouthwash. The FDA has been apprised of the action. The mouthwash has been tested and been found positive for Burkholderia cepacia (B. cepacia). The CDC has confirmed hospital illnesses in one state associated with the use of the affected mouthwash.
Product was distributed to hospitals, medical centers, and long term care facilities nationwide.
B. cepacia poses little medical risk to healthy people. However, people who have certain health problems such as weakened immune systems or chronic lung diseases, particularly cystic fibrosis (CF), may be more susceptible to infections with B. cepacia. B. cepacia is a known cause of infections in hospitalized patients. B. cepacia bacteria are often resistant to common antibiotics. The effects of B. cepacia on people vary widely, ranging from no symptoms at all, to serious respiratory infections, especially in patients with CF.
The recall includes the following products:
Description | Reorder Number |
|---|---|
Alcohol-Free Mouthwash, Cardinal Health, 4 oz. | AG-210 |
Product lot number 26228 is affected. Affected product can be identified by checking the lot code stamped on the Cardinal Health label. The Lot number is located on the side of the bottle.
The mouthwash may also be found in certain Personal Hygiene Hospital Admission Kits. If you received mouthwash labeled for Cardinal Health from your healthcare provider, please check to see if the reorder number on the label matches the recalled reorder numbers listed above, then check to see if the lot number matches the recalled lot number.
Customers who have Cardinal Health labeled alcohol free mouthwash which is being recalled should stop using the product and contact Cardinal Health for instructions.
Cardinal Health is notifying their customers via overnight mail and is arranging for all product to be returned for credit.
TJ Power Sports LLC Recalls Twister Hammerhead Dune Buggies.

| FOR IMMEDIATE RELEASE May 6, 2008 Release #08-262 | CPSC Recall Hotline: (800) 638-2772 |
TJ Power Sports Recalls Dune Buggies Due To Ejection Hazard
WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.Name of Product: Twister Hammerhead Dune Buggies
Units: About 400
Importer: TJ Power Sports LLC, of Irving, Texas
Hazard: The seat belt adjustment for the shoulder buckle can break during impact or stress, posing an ejection and injury hazard to driver and passenger.
Incidents/Injuries: TJ Power Sports has received one report of a seat belt breaking that resulted in nerve damage to the rider’s right arm.
Description: This recall involves the dune buggies “Twister Hammerhead” with model number UM150IIR and model year 2004. The dune buggies were available in red, blue, or green. “Twister Hammerhead”, the model number, and the model year can be found imprinted on the bar behind the driver and passenger seats.
Sold through: Twister dealers nationwide and online retailers from July 2004 through December 2004 for about $3,000.
Manufactured in: China
Remedy: Consumers should stop using these dune buggies immediately and contact TJ Power Sports for instructions on how to receive a replacement seat belt.
Consumer Contact: For additional information, visit the firm’s Web site www.tjpowersports.com
Playworld Systems Inc Recalls Playground Swing Sets.

| May 6, 2008 Alert #08-568 |
Playworld Systems Recalls Swing Sets Due to Fall Hazard Caused by Defective Clevises
The following product safety recall was voluntarily conducted by the firm in cooperation with the CPSC. Consumers should stop using the product immediately unless otherwise instructed.
Name of Product: Playground Swing Sets
Units: About 17,300
Manufacturer: Playworld Systems Inc., of Lewisburg, Pa.
Hazard: The clevis bearing on the swing set can wear, causing the swing to detach and the user to fall.
Incidents/Injuries: No incidents or injuries have been reported.
Description: Swing sets involved in this recall have the following part numbers:
| 8 ft 2-Unit Standard Swing | 0248 | 5 in Arch Swing w-8 ft Top Rail | 0287 |
| 8 ft Standard Duty Swing Add-A-Bay | 0230 | 5 in Arch Swing 2-Unit Add-A-Bay | 0370 |
| 10 ft 2-Unit Standard Swing | 0249 | 3-1/2 in Arch Swing w-8 ft Top Rail | 0288 |
| 10 ft Standard Duty Swing Add-A-Bay | 0231 | 3-1/2 in Arch Swing Add-A-Bay | 0375 |
| 8 ft 2-Unit Heavy Duty Swing | 0270 | 2-3/8 in Arch Swing w-7 ft Top Rail | 0120 |
| 8 ft heavy duty swing add-a-bay | 0232 | 2-3/8 in Arch Swing Add-A-Bay | 0121 |
| 10 ft 2-Unit Heavy Duty Swing | 0259 | 7 ft Early Childhood T-Swing | 0290 |
| 10 ft Heavy Duty Swing Add-A- Bay | 0233 | ||
| 8 ft Single Post Swing Assembly | 0295 | ||
| 8 ft Single Post Swing Add-A- Bay | 0296 |
Sold by: Authorized dealers sold the swing sets to day care centers and children’s learning centers nationwide from January 2007 through February 2008 for about between $770 and $3,100.
Manufactured in: United States
Remedy: Consumers should immediately remove the swing from the swing set until a free repair kit is installed. The company has sent direct mail notices to consumers.
Consumer Contact: For additional information, contact Playworld Systems at (800) 233-8404 between 8 a.m. and 5 p.m. ET Monday through Friday, or visit the firm’s Web site at www.playworldsystems.com