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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.
Consumers and health professionals are advised that Beijing Tong Ren Tang Australia in consultation with the TGA is recalling
Batch 16080020 and Batch 4080015 of Bronchi-cough Pills (qiguanyan
kesou tanchuanwan; AUST L 144659) due to contamination with substances
that pose an unacceptable risk to health.
TGA testing has found that both currently available batches of the
product are contaminated with low levels of amygdalin. One batch
(16080020) is also contaminated with very low levels of aristolochic
acid. Both amygdalin and aristolochic acid are included in Schedule 10
to the Poisons Standard, which lists substances considered to pose an unacceptable risk to health.
There is no established safe exposure level to aristolochic acids,
which have been linked to kidney problems and urinary tract cancers.
Information for consumers
If you or someone you provide care for takes Bronchi-cough Pills,
please be alert to this issue and discontinue use immediately. The
product should not be consumed.
If you have any Bronchi-cough Pills, the remaining product can be returned to the place of purchase for a refund.
If you have any questions or concerns about this issue, talk to your health professional or contact 1300 287 828.
Information for health professionals
Please be aware of the above issue and advise patients regarding alternative treatment options if they seek advice.
If you have any questions or concerns about this issue, contact 1300 287 828.
Reporting problems
Consumers and health professionals are encouraged to report problems with medicines or vaccines. Your report will contribute to the TGA's monitoring of these products.
The TGA cannot give advice about an individual's medical condition.
You are strongly encouraged to talk with a health professional if you
are concerned about a possible adverse event associated with a medicine
or vaccine.
Bone-In-Half Leg of Ham 4.5kg Best Before 29/01/2019
Identifying features
Best before date
29 January 2019
What are the defects?
The recall is due to microbial (Listeria monocytogenes) contamination.
What are the hazards?
Listeria may cause illness in pregnant women and their unborn babies, the elderly and people with low immune systems.
What should consumers do?
Consumers concerned about their health should seek medical advice and should return the product to the place of purchase for a full refund. For further information please contact:
Bio-Blue Fluid, Bio-Blue Toilet Deodorant and Bio-Green Digester
Product description
This recall involves the following products:
Name of Chemical
Volume
UPC
Bio-Green Digester
12 x 0.5 oz self-dissolving pouches
060823265208
Bio-Blue Fluid
16oz / 473ml bottle
060823261606
Bio-Blue Toilet Deodorant
12 x 0.5 oz self-dissolving pouches
060823264201
Hazard identified
Health Canada has determined that the recalled product does not meet the chemical hazard labelling and child-resistant packaging for consumer products as set out in the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act.
Improper packaging or labelling could result in unintentional exposure to these products and lead to serious illness, injury or death.
As of December 18, 2018, no incidents or injuries were reported to the company regarding the use of this product in Canada.
Number sold
Approximately 50,840 units of the affected products were sold in Canada.
Time period sold
The affected products were sold from January 2006 to December 2018.
Most federal services are closed due to government shutdown. I have only noticed one recall on FDA site them. Other entities like, USDA, CDC, HHS, CPSC, NHTSA and EPA have not released any recall since.
We will keep on looking.
As I recall most recalls happens during the holiday season due to various reasons. Wish you all a safe holidays.
Every department has a similar message as shown below;
FDA Lapse in Funding
In the absence of either an FY 2019 appropriation or a Continuing Resolution for FDA, beginning on December 22, 2018 and continuing until the date of enactment of an FY 2019 appropriation or Continuing Resolution ("lapse period"), agency operations continue to the extent permitted by law, such as activities necessary to address imminent threats to the safety of human life and activities funded by carryover user fee funds.
Due to a lapse in appropriations, EPA websites will not be regularly updated. In the event of an environmental emergency imminently threatening the safety of human life or where necessary to protect certain property, the EPA website will be updated with appropriate information. Please note that all information on the EPA website may not be up to date, and transactions and inquiries submitted to the EPA website may not be processed or responded to until appropriations are enacted.
Following
observation of variable burst pressure performance of Polyisoprene
Condoms manufactured during 2017, Reckitt Benckiser Canada conducted an
internal investigation and identified that a specific batch (1000356816)
of DUREX RealFeel® 20 ct condoms distributed in Canada is not expected
to meet the registered burst pressure specification at end of
shelf-life. As a cautionary measure, Reckitt Benckiser Health (Canada)
Inc. is initiating a consumer level recall.
Starting date:
December 26, 2018
Posting date:
December 27, 2018
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Following observation of variable burst pressure performance of Polyisoprene Condoms manufactured during 2017, RB conducted an internal investigation and identified that a specific batch (1000356816) of DUREX RealFeel® 20 ct condoms distributed in Canada is not expected to meet the registered burst pressure specification at end of shelf-life. As a cautionary measure, RB Health (Canada) Inc. is initiating a consumer level recall.
