Drug Recall: Antica Ocean Citron Hand Sanitizer Gel

Drug Recall: Antica Ocean Citron Hand Sanitizer Gel

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US FlagUS/Silver Spring: Salon Technologies International. Inc., an Orlando, Florida.establishment, recalls an estimated 512 bottles of Antica Ocean Citron Hand Sanitizer Gel from the American marketplace due to suspected Benzene chemical contamination 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-altering injury or death.

FDA: https://bit.ly/3dCRQ0h

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/salon-technologies-inc-issues-voluntary-nationwide-recall-antica-ocean-citron-hand-sanitizer-alcohol

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

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Drug Recall: Banana Boat Hair & Scalp Sunscreen Spray

Banana Boat Hair & Scalp Sunscreen Spray

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US FlagUS/Silver Spring: Edgewell Personal Care Company, a Shelton, Connecticut establishment, recalls certain batch/lots of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 from the American marketplace due to suspected Benzene chemical contamination 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-altering injury or death.

FDA: https://bit.ly/3oWnNmw

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/edgewell-personal-care-issues-voluntary-nationwide-recall-banana-boat-hair-scalp-sunscreen-due

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

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Suave Aerosol Antiperspirants [US]

Suave Aerosol Antiperspirants [US]

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US FlagUS/Silver Spring: Unilever, an Englewood Cliffs, New Jersey establishment, recalls certain batch/lots of two Suave 24-Hour Protection Aerosol Antiperspirants 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/376P30sgN6I

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/unilever-issues-voluntary-nationwide-recall-suave-24-hour-protection-aerosol-antiperspirant-powder

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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Mandalorian & Mickey Mouse Hand Sanitizers [US]

Mandalorian & Mickey Mouse Hand Sanitizer Ethyl Alcohol Recall [US]

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US FlagUS/Silver Spring: Best Brands Consumer Products, Inc., a Merrick, New York establishment, recalls certain batch/lots of The Mandalorian Hand Sanitizer Ethyl Alcohol 68%, and Mickey Mouse Hand Sanitizer Ethyl Alcohol 68% from the American marketplace due to reported presence of Benzene in The Mandalorian Hand Sanitizer product and Methanol in the Mickey Mouse Hand Sanitizer product and consequential risks of various Cancers, Blindness, Central Nervous Damage and other conditions, 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/eYWi30sgzHz

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/best-brand-consumers-products-inc-issues-voluntary-recall-mickey-mouse-hand-sanitizer-ethyl-alcohol

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products 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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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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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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Neutrogena & Aveeno Aerosol Sunscreen Recall [US]

Neutrogena and Aveeno Aerosol Sunscreen Recall [US]

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US FlagUS/Silver Spring: Johnson & Johnson Consumer Inc., a New Brunswick, New Jersey establishment, recalls all current batch/lots of five (5) Neutrogena and Aveeno Aerosol Sunscreen product lines from the American marketplace due to suspected Benzene contamination, a consequential Carcinogen, a substance or agent known to cause or reasonably expected to cause Cancer, a serious health and safety hazard requiring intervention and/or treatment.

FDA: http://ht.ly/ut2z30rNX6w

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/johnson-johnson-consumer-inc-issues-voluntary-recall-specific-neutrogenar-and-aveenor-aerosol

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

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