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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Product Recall: Fixodent, KY Jelly, Opti Free & Poligrip

US FlagUS/Silver Spring: Logo - Family DollarFamily Dollar, a Charlotte, North Carolina establishment, recalls numerous non-drug products regulated by the US Food and Drug Administration (“FDA”) that were stored and shipped to most Family Dollar stores on or around May 1, 2022 through June 10, 2022.

This recall was initiated after it was determined that these products were stored outside of labeled temperature requirements with consequential risks of spoilage, deactivation of protective and/or medicinal ingredients, in-use operational failure and/or 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: https://bit.ly/3LopmUJ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-certain-over-counter-products-sold-family-dollar-stores-because-they-were-stored

Additional information:
The US Food and Drug Administration (“FDA”) reports the following non-drug products regulated by the US FDA are subject to this recall (in alphabetical order):

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Product, Toy & Vehicle Recalls in the European Union

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 37/2022 of its Rapid Alert System containing thirty-four (34) 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: https://bit.ly/3Ln8PAb

Direct EU: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000115?lang=en

Additional information:
Among the thirty-four (34) recalls the European Union announced in its third report of September 2022, the following recall notification was made:
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Drug Recall: Colgate Toothpaste & Mouthwash

Drug Recall: Colgate Toothpaste and Mouthwash

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US FlagUS/Silver Spring: Family Dollar, a Charlotte, North Carolina establishment, recalls certain batch/lots of Colgate Toothpaste and Mouthwash from the American marketplace and sold at Family Dollar Stores due to suspected product storage outside of labeled temperature requirements and consequential risks of spoilage and 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: https://bit.ly/3BncARC

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-certain-colgate-products-sold-family-dollar-stores-because-they-were-stored-outside

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

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Product, Toy & Vehicle Recalls in the European Union

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 36/2022 of its Rapid Alert System containing twenty-two (22) 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: https://bit.ly/3qqEw1P

Direct EU: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000114?lang=en

Additional information:
Among the twenty-two (22) recalls the European Union announced in its second report of September 2022, the following recall notification was made:
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Product, Toy & Vehicle Recalls in the European Union

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 35/2022 of its Rapid Alert System containing thirty-one (31) 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: https://bit.ly/3RrQ9kL

Direct EU: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10006677?lang=en

Additional information:
Among the thirty-one (31) recalls the European Union announced in its first report of September 2022, the following recall notification was made:
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Product, Toy & Vehicle Recalls in the European Union

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 34/2022 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: https://bit.ly/3e0eb81

Direct EU: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000112

Additional information:
Among the forty-four (44) recalls the European Union announced in its fourth (and final) report of August 2022, the following recall notification was made:
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Product, Toy & Vehicle Recalls in the European Union

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 33/2022 of its Rapid Alert System containing twenty-nine (29) 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: https://bit.ly/3QXk5F5

Direct EU: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000111

Additional information:
Among the twenty-nine (29) recalls the European Union announced in its third report of August 2022, the following recall notification was made:
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Product, Toy & Vehicle Recalls in the European Union

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 32/2022 of its Rapid Alert System containing thirty (30) 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: https://bit.ly/3QnPWPm.

Direct EU: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000110

Additional information:
Among the thirty (30) recalls the European Union announced in its second report of August 2022, the following recall notification was made:
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Product, Toy & Vehicle Recalls in the European Union

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 31/2022 of its Rapid Alert System containing twenty-nine (29) 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: https://bit.ly/3JxPk7c

Direct EU: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000109

Additional information:
Among the twenty-nine (29) recalls the European Union announced in its first report of August 2022, the following recall notification was made:
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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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Drug Recall: Sask Prairie Dill Pickle Flavoured Vodka

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Canada/Ottawa: Logo - Minhas Sask Ventures Inc.,Minhas Sask Ventures Inc., a Regina, Saskatchewan establishment, recalls certain batch/lots of Sask Prairie branded Dill Pickle Flavoured Vodka from the Canadian marketplace due to suspected glass fragment contamination and consequential risks of choking, oral injury, internal ingestion, GI tract laceration damage, bowel obstruction and sepsis, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CFIA: https://bit.ly/3OZsQgq

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/sask-prairie-brand-dill-pickle-flavoured-vodka-recalled-due-pieces-glass

Additional information:
The Canadian Food Inspection Agency (“CFIA”) reports the following Vodka products are subject to this recall:

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Product, Toy & Vehicle Recalls in the European Union

European Union FlagBelgium/Brussels: European Union Headquarters BrusselsThe European Union issues Report 30/2022 of its Rapid Alert System containing twenty-seven (27) 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: https://bit.ly/3PP5Q4Z

Direct EU: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000108

Additional information:
Among the twenty-seven (27) recalls the European Union announced in its fifth (and final) report of July 2022, the following recall notification was made:
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Drug Recall: Ultra Supplement Launch Sequence Capsules

Drug Recall: Ultra Supplement Launch Sequence Supplements

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US FlagCanada FlagUS/Silver Spring: Ultra Supplement LLC., a Wilmington, Delaware establishment, recalls certain batch/lots of Launch Sequence Aphrodisia and Euphoria Supplement Capsules 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:  https://bit.ly/3SblDwC

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/loud-muscle-science-llc-issues-voluntary-recall-launch-sequence-capsules-due-presence-undeclared

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

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Drug Recall: Sustango Nutritional Supplement Capsules

Drug Recall: Sustango Nutritional Supplement Capsules

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US FlagUS/Silver Spring: Ultra Supplement LLC, a Wilmington, Delaware establishment, recalls certain batch/lots of Sustango Nutritional Supplement Capsules 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: https://bit.ly/3Bviy4y

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ultra-supplement-llc-issues-voluntary-nationwide-recall-sustango-due-presence-undeclared-tadalafil

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

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