Fisher-Price Rock ‘n Play Baby Sleeper Recall [Australia]

Fisher-Price Rock 'N Play Sleeper Recall [Australia]

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Australia FlagMattel Pty Ltd, a Richmond, Melbourne establishment, recalls all models of the Fisher-Price branded Rock ‘n Play Baby Sleepers due to suspected failure to secure the infant and consequential risk of choking, asphyxiation and death, all serious health and safety hazards.

ACCC: http://ht.ly/e1TY30oKQRh

Direct link: https://www.productsafety.gov.au/recall/mattel-pty-ltd-fisher-price-rock-n-play-sleeper

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Rock ‘n Play Baby Sleepers.

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Triple Pearl Yellow Walking Siluriformes Fish Recall [US]

Triple Pearl Yellow Walking Siluriformes Fish Recall [US]

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US FlagUS/Washington: Trading Corp., a Los Angeles, California establishment, recalls an estimated 36,040 pounds of frozen Siluriformes products, specifically Yellow Walking Fish due to suspected failure to present for import re-inspection upon entry into the United States, a serious health and safety hazards.

USDA: http://ht.ly/Qcsf30oKNOM

Direct link: https://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2019/recall-052-2019-release

Additional information:
The United States Department of Agriculture (“USDA”) reports the following Siluriformes, specifically Yellow Walking Fish, and are subject to this recall:

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Hush Anesthetic Gel, Spray & Soap Recall [US]

Hush Anesthetic Gel, Spray & Soap Recall [US]

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US FlagUS/Washington: DDA Distributors, Inc., doing business as Hush Anesthetic, Inc., a Miami Lakes, Florida, recalls an estimated 275,000 Anesthetic Gels, Sprays and Foam Soaps due to suspected failure to meet US child resistant closure requirement and consequential risk of poisoning, ingestion and GI tract laceration damage, all serious health hazards.

CPSC: http://ht.ly/oo1830oKe64

Direct link: https://www.cpsc.gov/Recalls/2019/Hush-Recalls-Anesthetic-Gels-Sprays-and-Foam-Soaps-Due-to-Failure-to-Meet-Child-Resistant-Closure-Requirement-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Hush branded Anesthetic Gels, Sprays and Foam Soaps products containing 4% Lidocaine. The Gel and Spray produtcs were sold in two (2) and four (4)-ounce sizes while the Foam Soap was sold in 1.7-ounce size.

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EU issues 34 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 19/2019 of its Rapid Alert System containing 34 consumer, automotive 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/mLvK30oHAqR

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=3402&Year=2019&lng=en

Additional information:
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Stiff Boy branded Beast Supplement Recall [US]

Stiff Boy branded Beast Supplement Recall [US]

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US FlagUS/Silver Spring: Stiff Boy LLC, a Westchester County, New York establishment, recalls all current batch/lots of The Beast Dietary Supplement Capsules due to suspected undeclared Sildenafil, an FDA approved drug for the treatment of Male Erectile Dysfunction in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors and consequential risk of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/FyMw30oHizo

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/stiff-boy-llc-issues-voluntary-nationwide-recall-beast-capsules-due-presence-undeclared-sildenafil

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

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EU issues 33 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 18/2019 of its Rapid Alert System containing 33 consumer, automotive 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/G6xP30oDm1s

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=3392&Year=2019&lng=en

Additional information:
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Life Rising Dietary Supplement Recall [US]

Life Rising Dietary Supplement Recall [US]

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US FlagUS/Silver Spring: Life Rising Corporation, a Willowbrook, Illinois establishment, recalls all current Life Rising Holder-W Holder Warmer Capsules, Life Rising Neck-ND Neck Clear Capsules and HoliCare Metabolism Cleansing (MET-CLS) Tablets due to suspected risk of Lead contamination in excess of that allowed by federal regulation and consequential risk of a wide variety of symptoms, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/fNAc30oD6Mm

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/life-rising-corporation-recalls-chinese-herbal-supplements-because-possible-health-risk

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

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