Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

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US/Silver Spring: Lupin Pharmaceuticals, Inc., a Baltimore, Maryland establishment, recalls all current batch/lots of Lupin Pharma branded Metformin Hydrochloride Extended Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/NuJP30qY97Z

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lupin-pharmaceuticals-inc-issues-voluntarily-nationwide-recall-metformin-hydrochloride-extended

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Metformin medications are subject to this recall:

EU issues 75 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 28/2020 of its Rapid Alert System containing seventy five (75) consumer, automotive, commercial and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/afjI30qXHdZ

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000002&Year=2020&lng=en

Additional information:

All Clean Hand Sanitizer & Disinfectant Recall [US]

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US/Silver Spring: ITECH 361, a Sunland Park, New Mexico establishment, recalls an estimated 18,940 bottles of All Clean Hand Sanitizer, Moisturizer and Disinfectant products from the American marketplace due to the suspected presence of Methanol (also called Methyl Alcohol or “Wood Alcohol”), with consequential risk of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/fw4830qXUvF

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/itech-361-issues-voluntary-nationwide-recall-all-clean-hand-sanitizer-and-moisturizer-and

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall:

Saniderm Advanced Hand Sanitizer Recall [US]

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US/Silver Spring: Saniderm Products (“Saniderm”), a San Francisco, California establishment, recalls certain batch/lots of Saniderm Advanced Hand Sanitizer products from the American marketplace due to suspected presence of Methanol (also called Methyl Alcohol or “Wood Alcohol”), with consequential risks of poisoning, oral injury, internal ingestion, GI tract damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/OgdU30qXMcu

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/saniderm-products-voluntarily-issues-regional-virginia-maryland-new-jersey-recall-1-l-saniderm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall:

Shanghai Lansheng N95 Respirator Mask Warning [Canada]

Canada/Ottawa: Health Canada, an Ottawa, Ontario regulatory and safety authority, warns Canadians against buying and/or using reportedly counterfeit N95 Respirator Masks made by Shanghai Lansheng Light Industrial Products due to suspected failure to protect wearers against the SARS-CoV-2 virus and consequential risk of COVID-19 (also known as “Coronavirus”) infection as well as consequential heart, lung and kidney, brain damage, all serious health and safety hazards.

HCSC: http://ht.ly/EbIH30qXb2d

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73493a-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports that it has received reports that counterfeit N95 Respirator Masks produced by Shanghai Lansheng Light Industrial Products have been marketed, sold and delivered in Canada. These products falsely claim to protect wearers against COVID-19 and are reportedly being sold to Canadians online and in some retail stores.

Granules Pharma Metformin Hydrochloride Recall [US]

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US/Silver Spring: Granules Pharmaceuticals, Inc., a Chantilly, Virginia establishment, recalls twelve (12) batch/lots of Metformin Hydrochloride Extended-Release Tablets USP, 750 mg from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/dXLm30qX5hG

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/granules-pharmaceuticals-inc-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Metformin medications are subject to this recall:

EU issues 37 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 27/2020 of its Rapid Alert System containing thirty seven (37) consumer, automotive, commercial and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/UoYX30qVMWh

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000001&Year=2020&lng=en

Additional information:

TTDeye Contact Lens Recall [US]

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US/Silver Spring: Chengdu Ai Qin E-commerce Co., Ltd. recalls an estimated 1362 pairs of TTDeye branded Colored Contact Lenses from the American marketplace due to suspected failure to gain FDA mandatory pre-sale safety approvals and risk of eye damage and/or blindness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/IOr530qUB5Y

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/chengdu-ai-qin-e-commerce-co-ltd-issues-nationwide-recall-ttdeye-brand-colored-contact-lenses

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Colored Contact Lenses are subject to this recall:

EU issues 44 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 26/2020 of its Rapid Alert System containing forty four (44) consumer, automotive, commercial and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/p9tr30qTxtY

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000000&Year=2020&lng=en

Additional information:

Hoffmann-La Roche Perjeta-Herceptin Kit Recall [Canada]

Canada/Ottawa: Hoffmann-La Roche Limited, a Mississauga, Ontario establishment, recalls certain batch/lots of A. Perjeta-Herceptin Kit Powder from the Canadian marketplace due to suspected Glass Fragment contamination and consequential risk of internal laceration, both serious health and safety hazards.

HCSC: http://ht.ly/MKBe30qU61x

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73443r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following medications are subject to this recall:

Canon Ultimax-i Medical Imaging Device Recall [Canada]

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Canada/Ottawa: Canon Medical Systems Canada, a Markham, Ontario establishment, a subsidiary of Canon Medical Systems Corporation of Otawara-shi, Tochigi, Japan, recalls an unknown number of Ultimax-i Medical Imaging Devices from the Canadian marketplace due to suspected imaging inconsistencies and consequential incorrect patient diagnostics, potential treatment delays and poor patient outcomes, all serious health and safety hazards.

HCSC: http://ht.ly/agBT30qTR5i

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73299r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following medical devices are subject to this recall:

Visibly Clean branded Hand Sanitizer Recall [Canada]

Canada/Ottawa: Brands International Corporation, a Newmarket, Ontario establishment, recalls an unknown amount of Visibly Clean branded Hand Sanitizer products from the Canadian marketplace due to the reported failure to receive written authorization prior to the manufacturer and sale of a product that uses Technical-Grade Ethanol with possible risks of poisoning, oral injury, internal ingestion and GI tract laceration damage, all serious health and safety hazards.

HCSC: http://ht.ly/JW4K30qSxeH

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73407r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Ethanol-based Hand Sanitizer products are subject to this recall:

EU issues 28 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 25/2020 of its Rapid Alert System containing twenty eight (28) consumer, automotive, commercial and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/nClr30qSbyo

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=26&Year=2020&lng=en

Additional information:

GermZero Gel Hand Sanitizer Recall [Canada]

Canada/Ottawa: Flash Beauté Inc., a Laval, Quebec establishment, recalls an unknown amount of GermZero Gel Hand Sanitizer products from the Canadian marketplace due to the suspected presence of Denatured Alcohol-2-Isopropanol (DA-2I), a type of Ethanol deliberately rendered poisonous by the addition of hard-to-separate toxic substances with consequential risk of poisoning, oral injury, internal ingestion and GI tract laceration damage, all serious health and safety hazards

HCSC: http://ht.ly/l2Wg30qRX6U

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73393r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Ethanol-based Hand Sanitizer products are subject to this recall:

GSK Children’s Dimetapp & Robitussin Recall [US]

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US/Silver Spring: GSK Consumer Healthcare, a Warren, New Jersey establishment, recalls two batch/lots of Children’s Robitussin Honey Cough and Chest Congestion DM and one lot of Children’s Dimetapp Cold and Cough from the American marketplace due to suspected inclusion of incorrect dosing cups and consequential risks of medication overdose and/or medication under-dosage, all serious health hazards.

FDA: http://ht.ly/bC3e30qRUAQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gsk-consumer-healthcare-issues-voluntary-nationwide-recall-childrens-robitussinr-honey-cough-and

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Children’s medications are subject to this recall: