Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 21/2023 of its Rapid Alert System containing ninety-three (93) 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://rb.gy/otkhh.

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000150?lang=en

Additional information:
Among the ninety-three (93) recalls the European Union announced in its fourth (and final) report of May 2023, the following recall notification was made:

Drug Recall: Nature’s Energy Colostrum Supplements

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US/Silver Spring: Nature’s Energy, a Pleasant Grove, Utah establishment, recalls certain batch/lots of Nature’s Energy Children’s Chewable Colostrum Supplements from the American marketplace due to suspected mislabeling and consequential undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: https://rb.gy/dcepm

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natures-energy-issues-allergy-alert-undeclared-milk-childrens-chewable-colostrum-products

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

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 20/2023 of its Rapid Alert System containing one-hundred-and-seven (107) 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/3BLAabb.

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000149?lang=en

Additional information:
Among the one-hundred-and-seven (107) recalls the European Union announced in its third report of May 2023, the following recall notification was made:

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 19/2023 of its Rapid Alert System containing fifty-four (54) 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/3nWaaqn.

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000148?lang=en

Additional information:
Among the fifty-four (54) recalls the European Union announced in its second report of May 2023, the following recall notification was made:

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 18/2023 of its Rapid Alert System containing eighty-two (82) 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/3HP8J3L.

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000147?lang=en

Additional information:
Among the eighty-two (82) recalls the European Union announced in its first report of May 2023, the following recall notification was made:

Drug Recall: Gear Isle Dietary Supplements

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US/Silver Spring: Gear Isle, a West Sacramento, California establishment, recalls certain batch/lots of Pro Power Knight Plus Capsule Supplements, NUX Male Enhancement Capsule Supplements and Dynamite Super Capsule Supplements from the American marketplace due to reported undeclared Sildenafil and Tadalafil, FDA approved drugs 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/3HzBfq1

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gear-isle-issues-voluntary-nationwide-recall-pro-power-knight-plus-nux-male-enhancement-and-dynamite

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

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 17/2023 of its Rapid Alert System containing ninety-two (92) 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/40QFhRA.

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000146?lang=en

Additional information:
Among the ninety-two (92) recalls the European Union announced in its fourth (and final) report of April 2023, the following recall notification was made:

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 16/2023 of its Rapid Alert System containing ninety (90) 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/3AlXBao.

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000145?lang=en

Additional information:
Among the ninety (90) recalls the European Union announced in its third report of April 2023, the following recall notification was made:

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 15/2023 of its Rapid Alert System containing one-hundred-and-eight (108) 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/3MHixA8.

Direct: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000144?lang=en

Additional information:
Among the one-hundred-and-eight (108) recalls the European Union announced in its second report of April 2023, the following recall notification was made:

Drug Recall: Dr. Rico Perez Super Kids Colostrum Tablets

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US/Silver Spring: Rico Perez Products, Inc., a Miami, Florida establishment, recalls certain batch/lots of Dr. Rico Perez Super Kids Colostrum Chewable Tablets from the American marketplace due to suspected mislabeling and consequential undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

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

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/rico-perez-products-inc-issues-allergy-alert-undeclared-milk-super-kids-colostrum

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

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 14/2023 of its Rapid Alert System containing fifty-nine (59) 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/3Gmq0AL.

Direct: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000143?lang=en

Additional information:
Among the fifty-nine (59) recalls the European Union announced in its first report of April 2023, the following recall notification was made:

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 13/2023 of its Rapid Alert System containing thirty-eight (38) 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/3nFVfQR.

Direct: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000142?lang=en

Additional information:
Among the thirty-eight (38) recalls the European Union announced in its fifth (and final) report of March 2023, the following recall notification was made:

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 12/2023 of its Rapid Alert System containing sixty-one (61) 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/3ZddZ7o.

Direct: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000141?lang=en

Additional information:
Among the sixty-one (61) recalls the European Union announced in its fourth report of March 2023, the following recall notification was made:

Product, Toy & Vehicle Recalls in the European Union

Belgium/Brussels: The European Union issues Report 11/2023 of its Rapid Alert System containing sixty (60) 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/3Jo0pbk.

Direct: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000140?lang=en

Additional information:
Among the sixty (60) recalls the European Union announced in its third report of March 2023, the following recall notification was made:

Drug Recall: Dr. Rima Recommends Nano Silver Supplements

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US/Silver Spring: Natural Solutions Foundation, a Newton, New Jersey establishment, recalls certain batch/lots of Dr. Rima Recommends Nano Silver Dietary Supplements from the American marketplace due to suspected unsubstantiated health claims that the product will prevent, treat, or cure COVID-19, claims that the FDA says may prevent patients who use this product from seeking timely medical treatment run the risk of serious, life-threatening health consequences, 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/3mTIBNr

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/urgent-notice-product-recall

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