Silver Bullet Male Enhancement Supplement Recall [US]

US FlagUS/Silver Spring: Logo - Silver BulletSpring: Nature’s Rx, a Claremont, California establishment, recalls batch/lots of Nature’s Rx Silver Bullet Male Enhancement 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/67hD30pTxfA

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natures-rx-issues-voluntary-nationwide-recall-silver-bullet-10-male-enhancement-capsules-due

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

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Up2 All Natural Libido Dietary Supplement Recall [US]

Up2 All Natural Libido Dietary Supplement Recall [US]

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US FlagUS/Silver Spring: Med Man Distribution, a Sault Ste. Marie, Ontario establishment, recalls certain batch/lots of Up2 There Is No Other All Natural Libido for Men & Women Dietary Supplements 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/8Bao30pSpI4

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/med-man-issues-voluntary-nationwide-recall-up2-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 31 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 45/2019 of its Rapid Alert System containing 31 (thirty one), 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/1gry30pR9ia

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=3662&Year=2019&lng=en

Additional information:
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Chubby Gumz Baby Soother Dummy Recall [Australia]

Bibs branded Infant Soothers/Dummies

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Australia FlagAustralia/Canberra: Chubby Gumz, an Australian eBay reseller, has recalled certain batch/lots of Bibs branded Infant Soothers/Dummies (Pacifiers) due to suspected failure to comply with Australia’s mandatory standard Consumer Goods (Babies Dummies and Dummy Chains) Safety Standard 2017 by providing the required the safety notice or hygienic care instructions and consequential risks of choking and/or strangulation, all serious health and safety hazards.

ACCC: http://ht.ly/qXpd30pRTAE

Direct link: https://www.productsafety.gov.au/recall/chubby-gumz-bibs-baby-dummies

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Bibs branded Baby Dummies / Pacifiers are subject to this recall:

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EU issues 68 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 44/2019 of its Rapid Alert System containing sixty-eight (68), 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/TJM030pPoLJ

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=3652&Year=2019&lng=en

Additional information:
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Fisherman’s Wharf Swai Fish Recall [US]

Fisherman's Wharf Swai Fish Recall [US]

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US FlagUS/Washington: H&T Seafood Inc., a Bell, California establishment, recalls an undetermined amount of Fisherman’s Wharf branded Swai Fillets, a type of Siluriformes Fish products, that were packed and distributed without the benefit of USDA inspection and used the mark of USDA inspection without official authorization, all serious health and safety hazards.

USDA: http://ht.ly/K49a30pPgcH

Direct link: https://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2019/recall-105-2019-release

Additional information:
The following Siluriformes Fish products were imported from Vietnam to the United States over an undetermined amount of time and are subject to this recall:

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Perrigo branded Ranitidine Recall [US]

US FlagUS/Silver Spring: Logo - Perrigo Company plcPerrigo Company plc, an Allegan, Michigan establishment and a subsidiary of Perrigo of Hogan Place, Dublin, Ireland, recalls all current batch/lots and package sizes of Ranitidine, a drug available OTC and by prescription within the United States, due to a specific Nitrosamine contamination called N-nitrosodimethylamine (“NDMA”), a probable human Carcinogen, a substance that could cause Cancer, all serious health hazards.

FDA: http://ht.ly/Msef30pNfyx

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/perrigo-company-plc-issues-voluntary-worldwide-recall-ranitidine-due-possible-presence-impurity-n

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

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