Product Recall: Amazon & Walmart Children’s Butterfly Nets

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Product Recall: Amazon, BedBathBeyond Walmart Children's Butterfly Nets

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Canada/Ottawa: Amazon.ca, a subsidiary of Seattle, Washington-based Amazon.com, BedBathandBeyond.ca, the Canadian subsidiary of a Bed Bath and Beyond, a Union, New Jersey establishment, and Walmart.ca, a Mississauga, Ontario establishment, recall certain batch/lots of Juvo Plus Children’s Butterfly Nets from the Canadian marketplace due to excessive levels of Lead and Phthalates (“DEHP”) and consequential risks to children of damage to the brain and nervous system, slowed growth and development, learning and behavior problems, hearing and speech problems, lower IQ, decreased ability to pay attention and underperformance in school. In adults, Lead poisoning can cause high blood pressure, joint and muscle pain, difficulties with memory or concentration, headache, abdominal pain, mood disorders, reduced sperm count and abnormal sperm, miscarriage, stillbirth and/or premature birth in pregnant women, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

HCSC: https://bit.ly/3N5M8l8

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/children-s-butterfly-net-juvo-plus-recalled-due-presence-lead-and-phthalates

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Juvo Plus Children’s Butterfly Nets are subject to this recall:

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Product Recall: Walmart & Amazon Army Action Figure Toys

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Product Recall: Walmart & Amazon Army Action Figure Toys Sets [Canada]

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Canada/Ottawa: Amazon.ca, a subsidiary of Seattle, Washington-based Amazon.com, and Walmart.ca, a Mississauga, Ontario establishment, recall certain batch/lots of Juvo Plus Army Action Figure Toys Sets from the Canadian marketplace due to excessive levels of Lead and Phthalates (“DEHP”) and consequential risks to children of damage to the brain and nervous system, slowed growth and development, learning and behavior problems, hearing and speech problems, lower IQ, decreased ability to pay attention and underperformance in school. In adults, Lead poisoning can cause high blood pressure, joint and muscle pain, difficulties with memory or concentration, headache, abdominal pain, mood disorders, reduced sperm count and abnormal sperm, miscarriage, stillbirth and/or premature birth in pregnant women, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

HCSC: https://bit.ly/3Tu2d6i

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/300-piece-army-action-figure-set-juvo-plus-recalled-due-presence-lead-and-phthalates

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

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Product Recall: Air Steward Portable Radon Monitors

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Product Recall: Air Steward Portable Radon Monitors

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Canada/Ottawa: Air Ae Steward, doing business as EcommerceTech OU, a Estonian establishment, recalls an estimated 100 Air Steward branded Portable Radon Monitors from the Canadian marketplace and sold on Amazon.ca due to reported operational failure and consequential risks of continued exposure to Radon with increased long-term chances of Cancer and other life-changing injuries, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

HCSC: https://bit.ly/3rcED1E

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/air-steward-portable-radon-monitor-recalled-due-inaccurate-radon-detection

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

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Brut Classic Aerosol Spray Deodorant [Canada]

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Brut Classic Aerosol Spray Deodorant [Canada]

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Canada/Ottawa: LZ Corp./K-G Spray-Pak, Inc., a Mississauga, Ontario establishment, recalls an estimated 8,600 cans of Brut Classic Aerosol Spray Deodorant from the Canadian marketplace due to elevated levels of Benzene and consequential risks of Cancers of the Blood and Blood-Forming Tissues, including the Bone Marrow and the Lymphatic System including Leukemia, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-changing injury.

HCSC: http://ht.ly/iT2L30scnPU

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/brut-classic-aerosol-spray-deodorant-recalled-due-potential-presence-benzene

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

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Ombrelle Garnier Dry Mist Spray Sunscreen [Canada]

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Ombrelle Garnier Complete Dry Mist Spray Sunscreen Recall [Canada]

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Canada/Ottawa: Ombrelle Canada, a Toronto, Ontario establishment and a subsidiary of Ombrella Marketing Company of Middletown, Delaware, a division of L’Oréal of Paris, France, recalls all current batch/lots of Ombrelle Garnier Complete Dry Mist Spray Sunscreen, SPF 30 and SPF 60, from the Canadian marketplace due to elevated levels of Benzene and consequential risks of Cancers of the Blood and Blood-Forming Tissues, including the Bone Marrow and the Lymphatic System including Leukemia, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-changing injury.

HCSC: http://ht.ly/JJlk30rXCuB

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/76663a-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Ombrelle Garnier Complete Dry Mist Spray Sunscreen products are subject to this recall:

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Pfizer Chantix (Varenicline) Tablet Recall [US]

Pfizer Chantix Tablet Recall [US]

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US FlagUS/Silver Spring: Pfizer, a Manhattan, New York establishment, recalls certain batch/lots of Chantix Tablets due to the presence of N-nitroso-varenicline contamination and consequential risks of increased carcinogenicity (Cancer), severe illness and/or possible life-changing complications, all serious health and safety hazards/situations requiring immediate medical intervention to minimize suffering and prevent life-changing injury.

FDA: http://ht.ly/sDqw30rRBS6

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-expands-voluntary-nationwide-recall-include-four-additional-lots-chantixr-varenicline-tablets

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

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Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/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:

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Granules Pharma Metformin Hydrochloride Recall [US]

Granules Pharma Metformin Hydrochloride Recall [US]

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US FlagUS/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:

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Apotex Metformin Hydrochloride Tablet Recall [Canada]

Apotex Metformin Hydrochloride Tablet Recall [US]

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Canada FlagCanada/Ottawa: Apotex Corp., a Toronto, Ontario establishment, recalls certain batch/lots of Apotex Corp branded Metformin Hydrochloride Extended-Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable Health Canada levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

HCSC: http://ht.ly/RIm630qRn75

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73339r-eng.php

Additional information:
The Health Canada (“HCSC) reports the following Metformin medications are subject to this recall:

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Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Lupin Pharmaceuticals, Inc., a Baltimore, Maryland establishment, recalls certain 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/GfnZ30qQfdN

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

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

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Apotex Metformin Hydrochloride Tablet Recall [US]

Apotex Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Apotex Corp., a Toronto, Ontario establishment, recalls certain batch/lots of Apotex Corp 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/HmUE30qPhSK

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/apotex-corp-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended-release-tablets

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

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Actavis Pharma Metformin Hydrochloride Tablet Recall [US]

Actavis Pharma Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Teva Pharmaceuticals USA, Inc., a Parsippany, New Jersey establishment and subsidiary of Teva Pharmaceutical Industries Ltd. of Petah Tikva, Israel, recalls certain batch/lots of Actavis Pharma, Inc. 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/q9Pu30qOed1

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-pharmaceuticals-usa-inc-initiates-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:

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Time-Cap Labs Metformin Hydrochloride Tablet Recall [US]

Time-Cap Labs Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Marksans Pharma Limited, a Verna, Goa, India establishment, recalls certain batch/lots of Time-Cap Labs, Inc. 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/upL630qNRGM

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/marksans-pharma-limited-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended-release

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

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Amneal Metformin Hydrochloride Tablet Recall [US]

Logo - Metformin Hydrochloride Extended Release Tablets

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US FlagUS/Silver Spring: Amneal Pharmaceuticals LLC, a Bridgewater, New Jersey establishment, recalls all current batch/lots of 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/pU8030qNxkW

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-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:

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American Health Ranitidine Tablet Recall [US]

American Health Ranitidine Tablet Recall [US]

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US FlagUS/Silver Spring: American Health Packaging, a Columbus, Ohio establishment, recalls eleven (11) lots of Ranitidine Tablets, USP 150 mg, 100 count Unit Dose Blisters from the American marketplace due to suspected levels of N-Nitrosodimethylamine (“NDMA”), a probable Human Carcinogen, above the allowable limits established by the FDA and consequential risk of Cancer, all serious health hazards.

FDA: http://ht.ly/gFcQ30qnOVO

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/american-health-packaging-issues-voluntary-nationwide-recall-ranitidine-tablets-usp-150-mg-100-count

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

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