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, 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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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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Food Recall: Mr. Right Keampferia Galanga Powder

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Food Recall: Mr. Right Keampferia Galanga Powder

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Canada/Ottawa: Ka Wing Hong, a Markham, Ontario establishment, recalls certain batch/lots of Mr. Right branded Keampferia Galanga Powder from the Canadian marketplace due to suspected Aconitine contamination and consequential risks of neurological, cardiovascular and gastrointestinal damage, 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.

CFIA: https://bit.ly/3eh4qCs

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/mr-right-brand-keampferia-galanga-powder-sand-ginger-powder-recalled-due-aconitine

Additional information:
The Canadian Food Inspection Agency (“CFIA”) reports the following Spice 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 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 Recall: Aesop Deodorizing Drops, Oil Burner Blends

Product Recall: Aesop Bathroom Deodorizing Drops and Oil Burner Blends

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US FlagCanada FlagUS/Bethesda & Canada/Ottawa: Aesop USA Inc., a New York, New York establishment and Aesop Canada Inc, a Vancouver. British Columbia establishment, recall an estimated total 176,200 of Aesop branded Bathroom Deodorizing Drops and Oil Burner Blends (approximately 154,300 in the US and approximately 21,900 in Canada) from the American and Canadian marketplaces due to suspected failure to meet US and Canadian child resistant closure requirements under the US Poison Prevention Packaging Act as well as Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act.

In addition, the recalled products reportedly violates the Federal Hazardous Substances Act (FHSA) by omitting the mandatory information on the packaging with consequential risks of child poisoning, aspiration, burns, ingestion and GI tract laceration damage, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CPSC: https://bit.ly/3wMgHp5; HCSC: https://bit.ly/3dPDKsr

Direct US link: https://www.cpsc.gov/Recalls/2022/Aesop-USA-Recalls-Bathroom-Deodorizing-Drops-and-Oil-Burner-Blends-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-and-Violation-of-FHSA-Labeling-Requirement-Risk-of-Poisoning

Direct Canada link: https://recalls-rappels.canada.ca/en/alert-recall/aesop-post-poo-drops-and-various-aesop-oil-burner-blends-recalled-due-lack-child

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Aesop Post-Poo Drops, a bathroom deodorizer product sold stand-alone in 100 mL amber glass bottles:

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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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Food Recall: Capri Sun Wild Cherry Flavored Juice Drink

Capri Sun Wild Cherry Flavored Juice Drink Recall [US]

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US FlagUS/Silver Spring: Kraft Heinz, a Chicago, Illinois and Pittsburgh, Pennsylvania establishment, recalls an estimated 5,760 cases of Capri Sun Wild Cherry Flavored Juice Drink Blend products from the American marketplace due to suspected cleaning fluid contamination and consequential risks of internal burns, liver damage, kidney damage, GI tract damage, 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/3prps3w

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kraft-heinz-announcing-voluntary-recall-capri-sun-wild-cherry-flavored-juice-drink-blend-beverages

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Flavored Children’s Drinks 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 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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Food Recall: Chaman Bahar Chomon Bahar Rose Powder

Food Recall: Chaman Bahar Chomon Bahar Rose Powder

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UK FlagUK/London: Green Foods International, an Oldham, Manchester, England establishment, recalls certain batch/lots of Chaman Bahar – Chomon Bahar Rose Powder from the British marketplace due to suspected unauthorised additive contamination and consequential risks of 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.

FSA: https://bit.ly/3djuf4t

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-40-2022

Additional information:
The UK Food Standards Agency (“FSA”) reports the following Spice products are subject to 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 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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Product Recall: Amazon NUK First Choice Baby Bottles

Amazon NUK First Choice Glass Baby Bottles Recall [US & Canada]

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US FlagCanada FlagUS/Bethesda & Canada/Ottawa: Astir Care Ltd., a Birmingham, England establishment, recalls an estimated total 175 NUK-branded First Choice Glass Baby Bottles (approximately 100 in the US and approximately 75 in Canada) sold on Amazon from the American and Canadian marketplaces due to suspected Lead chemical contamination 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.

CPSC: https://bit.ly/3OScuGg; HCSC: https://bit.ly/3d1NWNK

Direct US link: https://www.cpsc.gov/Recalls/2022/First-Choice-Glass-Baby-Bottles-Recalled-by-NUK-Due-to-Violation-of-the-Federal-Lead-Content-Ban-Sold-Exclusively-on-Amazon-com-Recall-Alert

Direct Canada link: https://recalls-rappels.canada.ca/en/alert-recall/nuk-first-choice-glass-baby-bottles-recalled-due-lead-excess-allowable-limit

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain NUK-branded First Choice Glass Baby Bottles, manufactured exclusively for the UK market and not intended for sale in the United States or Canada, as follows:

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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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