Equate Dry Mouth Oral Rinse Mouthwash [Canada]

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Equate Dry Mouth Oral Rinse Mouthwash Recall [Canada]

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Canada/Ottawa: The Shandex Sales Group, a Pickering, Ontario establishment, recalls an estimated 468 bottles of Equate branded Dry Mouth Oral Rinse Mouthwash products from the Canadian marketplace due to suspected Klebsiella pneumonia bacterial contamination and consequential risks of Gram-negative bacterial infection, healthcare-associated infections (“HAIs”), including Pneumonia, bloodstream infections, wound or surgical site infections and/or other life-changing complications, 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: http://ht.ly/3ZJL30s6sg2

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/equate-dry-mouth-oral-rinse-recalled-due-microbial-contamination

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

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Aussie, Herbal Essences, Pantene, Waterless Shampoo [US]

Aussie, Herbal Essences, Pantene, Waterless Shampoo [US]

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US FlagUS/Silver Spring: The Procter & Gamble Company (“P&G”), a Cincinnati, Ohio establishment, recalls certain batch/lots of Aerosol Dry Conditioner Spray products and Aerosol Dry Shampoo Spray products from Aussie, Herbal Essences, Pantene and Waterless produced in the United States, in addition to previously discontinued Aerosol Dry Shampoo products from Hair Food and Old Spice from the American 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.

FDA: http://ht.ly/16if30s4tsl

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pg-issues-voluntary-recall-aerosol-dry-conditioner-spray-products-and-aerosol-dry-shampoo-spray

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Aerosol Dry Conditioner Spray products and Aerosol Dry Shampoo Spray products are subject to this recall (in alphabetical order):

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Rompe Pecho Cold Remedy Products [US]:

US FlagUS/Silver Spring: Rompe Pecho Cold Remedy Recall [US]Efficient Laboratories, a Miami, Florida establishment, recalls certain batch/lots of Rompe Pecho CF, Rompe Pecho EX, Rompe Pecho MAX and Rompe Pecho DM Cold Remedy drug products from the American marketplace due to suspected unspecified microbial contamination and consequential risks of Gram-positive or Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: http://ht.ly/buRb30s3NRf

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/efficient-laboratories-inc-expands-voluntary-nationwide-recall-consumers-include-twelve-additional

Additional information:
The US Food and Drug Administration (“FDA”) reports the following over-the-counter (“OTC”) Cold Remedy drugs are subject to this recall:

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Odor-Eaters Spray Recall [US]

US FlagUS/Silver Spring: Odor-Eaters Spray Recall [US]Odor-Eaters, a division of Blistex Inc., a Oak Brook, Illinois establishment, recalls an estimated forty-one (41) batch/lots of two Odor-Eaters Spray products from the American 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.

FDA: http://ht.ly/RWVp30s1ugL

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/odor-eatersr-issues-voluntary-nationwide-recall-specific-lots-odor-eatersr-spray-powder-and-odor

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

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Mountain Meadow Candida Flush Supplement Recall [US]

Mountain Meadow Herbs Candida Flush Dietary Supplements Recall [US]

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US FlagUS/Silver Spring: Mountain Meadow Herbs, a Somers, Montana establishment, recalls certain batch/lots of Mountain Meadow Herbs branded Candida Flush Dietary Supplements from the American marketplace due to possible spoilage and consequential unexpected container depressurization with risks of eye damage, lung damage, bone fracture, laceration and/or property damage, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-changing injury.

FDA: http://ht.ly/4Tch30s195r

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mountain-meadow-herbs-recalls-supplement-product-due-exploding-bottle-risk

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

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TUMS Assorted Berries Tablets Recall [Canada]

TUMS Assorted Berries Extra Strength Tablets Recall [Canada]

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Canada FlagCanada/Ottawa: GSK Consumer Healthcare ULC, a Mississauga, Ontario and Laval, Quebec establishment, recalls certain batch/lots of TUMS Assorted Berries Extra Strength Tablets from the Canadian marketplace due to suspected to Metal Fragment contamination and consequential risks of choking, oral injury, internal ingestion, GI tract laceration damage and bowel obstruction, 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/AGoC30rZCNk

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/two-lots-tums-assorted-berries-extra-strength-tablets-recalled-because-they-may

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

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EU issues 33 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 43/2021 of its Rapid Alert System containing thirty-three (33) 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/c5VN30rYWQi

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000070

Additional information:
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EU issues 19 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 42/2021 of its Rapid Alert System containing nineteen (19) 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/tKLE30rXQhC

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000069

Additional information:
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Ombrelle Garnier Dry Mist Spray Sunscreen Recall [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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Tesco Flu-Max Chesty Cough & Cold Powder Recall [UK]

Tesco Flu-Max Chesty Cough & Cold Powder Recall [UK]

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UK FlagUK/London: Wrafton Laboratoires Limited (trading as Perrigo), a Wrafton, Braunton, Devon establishment, recalls certain batch/lots of Tesco Flu-Max All In One Chesty Cough & Cold Powder for Oral Solution (GSL) PL 12063/0104 from the British marketplace due to suspected mislabeling/mispackaging and consequential incorrect dosage with consequential risks of an overdose and/or underdose hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-changing injury

MHRA: http://ht.ly/dNaC30rX2cA

Direct link: https://www.gov.uk/drug-device-alerts/class-2-medicines-recall-tesco-flu-max-all-in-one-chesty-cough-and-cold-powder-for-oral-solution-wrafton-laboratoires-limited-trading-as-perrigo-el-21-a-slash-24#brief-description-of-the-problem

Additional information:
The UK Medicines & Healthcare Products Regulatory Agency (“MHRA”) reports the following Cough & Cold Powders are subject to recall:

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Genius Kids & Teens Health Supplement Recall [Canada]

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Genius Kids and Teens Natural Health Dietary Supplements Recall [Canada]

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Canada/Ottawa: Nutripur Inc., a Boisbriand, Quebec establishment, recalls one (1) known batch/lot of Genius Kids and Teens Natural Health Dietary Supplements from the Canadian marketplace due to suspected Staphylococcus aureus contamination and consequential risks of Gram-positive bacterial infection, severe illness and/or possible life-changing complications, 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/hGDA30rWMaj

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/76593a-eng.php

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

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GSK Advil Cold & Sinus Day/Night Drug Recall [Canada]

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GSK Advil Cold & Sinus Day/Night Drugs Recall [Canada]

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Canada/Ottawa: GlaxoSmithKline Consumer Healthcare ULC (“GSK”), a Mississauga, Ontario establishment, recalls certain batch/lots of Advil Cold & Sinus Day/Night Convenience Packs from the Canadian marketplace due to suspected mispackaging and/or mislabeling and consequential risks of incorrect dosing, inability to reliably operate machinery, falls, laceration, concussion, bone fractures and/or central nervous system (“CNS”) injury, 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/RZm330rW4dS

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/76571a-eng.php

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

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InterClinical Sym Balance Multi-Vitamin Recall [Australia]

Sym Balance 90 Multi-Vitamin Tablets

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Australia FlagAustralia/Canberra: InterClinical Laboratories Pty Ltd., an Alexandria, New South Wales establishment, recalls certain batch/lots of Sym Balance 90 Multi-Vitamin Tablets from the Australian marketplace due to suspected mislabeling and/or mispackaging and consequential undeclared allergens, sources of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, all serious health and safety hazards requiring immediate medical intervention to minimize suffering and prevent life-changing injury.

ACCC: http://ht.ly/UUAE30rSuqi

Direct link: https://www.productsafety.gov.au/recalls/interclinical-laboratories-pty-ltd-%E2%80%94-sym-balance-90-tablets

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following drug 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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Alpha Male Plus Male Enhancer Fruit Chew Recall [US]

Alpha Male Plus Male Enhancer Fruit Chew Recall [US]

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US FlagUS/Silver Spring: Alpha Male Plus, a Tucson, Arizona establishment, recalls all current batch/lots of Alpha Male Plus Male Enhancer Fruit Chew Supplements from the American marketplace due to reported undeclared Tadalafil, an FDA approved drug for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/8Vk130rOqJz

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/alpha-male-plus-issues-voluntary-nationwide-recall-alpha-male-plus-male-enhancer-due-presence

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

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