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:

S&B Golden Curry Medium Hot Sauce Mix Recall [UK]

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UK/London: JFC (UK) Limited, a London, England establishment, recalls certain batch/lots of S&B Golden Curry Medium Hot Sauce Mix from the British marketplace due to undeclared Celery and Mustard, both known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FSA: http://ht.ly/OvFE30qY7Ul

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-aa-43-2020

Additional information:
The UK Food Standards Agency (“FSA”) reports the following Golden Curry Sauce Mix products are subject to recall:

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:

River of Goods Ceiling Fan Recall [Canada]

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Canada/Ottawa: River of Goods, a St. Paul, Minnesota establishment, recalls an estimated 2,435 River of Goods branded Ceiling Fans from the Canadian marketplace due to suspected failure to incorporate the required secondary support cable within the design and consequential risks of attachment failure, impact injury, laceration, bone fracture and concussion, all serious safety hazards.

HCSC: http://ht.ly/mOSP30qXPVj

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73475r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves certain River of Goods branded Ceiling Fans.

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:

Sundial Herbal Dietary Supplement Recall [US]

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US/Silver Spring: Sundial Herbal Products, a Bronx, New York establishment, recalls all Sundial branded Dietary and Nutritional Supplement products, marketed, sold and delivered from January 1, 2014 to the date of this notification that have labeling that contains and/or make drug claims stating the product(s) can diagnose, cure, mitigate, treat or prevent any disease or condition.

FDA: http://ht.ly/gPQa30qXznA

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sundial-herbal-products-recalling-products-attached-because-these-products-were-misbranded-products

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

KIND Oats & Honey Granola with Coconut Recall [US]

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US/Silver Spring: KIND Healthy Snacks, a New York, New York establishment, recalls certain batch/lots of KIND branded Oats & Honey Granola with Toasted Coconut Pouches from the American marketplace due to undeclared Sesame Seeds, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/Si1l30qXmw4

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/allergy-alert-kind-issues-voluntary-recall-due-undeclared-sesame-seeds-oats-honey

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

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:

Bonds Poodlette Zip Wondersuit Recall [Australia]

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Australia/Canberra: Hanes Innerwear Australia Pty Ltd, a Victoria establishment, recalls certain batch/lots of Bonds Poodlette Zip Wondersuits due to suspected failure to carry the appropriate fire hazard information label as required by Australia’s mandatory standard ‘Consumer Goods (Children’s Nightwear and Limited Daywear and Paper Patterns for Children’s Nightwear) Safety Standard 2017’ and consequential risks of fire, burns and property damage, all serious health and safety hazards.

ACCC: http://ht.ly/CZor30qWWi9

Direct link: https://www.productsafety.gov.au/recall/hanes-innerwear-australia-pty-ltd-bonds-poodlette-zip-wondersuit-navy

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Children’s Clothing products are subject to this recall:

Kathmandu Karinjo Baby Carrier Recall [Australia]

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Australia/Canberra: Kathmandu, a South Melbourne, Victoria, establishment, recalls certain batch/lots of Kathmandu branded Karinjo Baby Carrier products from the Australian marketplace due to suspected component detachment and consequential risk of structural collapse, falls, lacerations, bone fractures and concussion, all serious safety hazards.

ACCC: http://ht.ly/k3Ha30qWF5W

Direct link: https://www.productsafety.gov.au/recall/kathmandu-karinjo-baby-carrier-40634-v2

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Baby Carrier products are subject to this recall:

Edens Garden Wintergreen Essential Oil Recall [US]

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US/Washington: Edens Garden, a San Clemente, California establishment, recalls an estimated 8,200 bottles of Wintergreen and Birch Essential Oils from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/Byhr30qWBjv

Direct link: https://www.cpsc.gov/Recalls/2020/Edens-Garden-Recalls-Wintergreen-and-Birch-Essential-Oils-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Wintergreen Essential Oil products, as follows:

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:

Whole Foods Market Red Velvet Cheesecake Recall [US]

US/Silver Spring: Whole Foods Market, an Austin, Texas establishment and subsidiary of Seattle, Washington-based Amazon.com recalls certain batch/lots of Carrot Cake Layered Cheesecake products labeled as Whole Foods Market branded Red Velvet Layered Cheesecake from the American marketplace and marketed, sold and delivered at 36 retail location of Whole Foods Market Stores in California, Idaho, and Nevada due to suspected mislabeling/mispackaging and consequential undeclared Walnuts, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/kkvX30qWnSJ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/allergy-alert-undeclared-tree-nut-red-velvet-cheesecake-slices-issued-whole-foods-market-stores

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

ThreeBond Liquid Gasket Recall [Canada]

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Canada/Ottawa: Royal Distributing, a Guelph, Ontario establishment and the importer of record, recalls an estimated 165 ThreeBond branded Liquid Gasket products manufactured by ThreeBond International of West Chester Township, Ohio from the Canadian marketplace due to reported failure to meet Canadian labelling and hazard information regulations and consequential risks of poisoning, inhalation, fire, burns, ingestion and GI tract laceration damage, all serious health and safety hazards.

HCSC: http://ht.ly/Cmjc30qWfW3

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73399r-eng.php

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