Grapefruit Vitamin C Unicorn Paper Mask Recall [US]

Grapefruit Vitamin C Unicorn Paper Mask Recall [US]

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US FlagUS/Silver Spring: Yes To Inc., a Pasadena, California establishment, recalls all current batch/lots of Grapefruit Vitamin C Glow-Boosting Unicorn Paper Mask products from the American marketplace due to risk of skin irritation and redness due to an unknown causality, both serious health hazards.

FDA: http://ht.ly/NYRn30qaEri

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/yes-inc-issues-voluntary-recall-product-due-skin-irritation-complaints-grapefruit-vitamin-c-glow

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

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Viande Richelieu Horse Meat Recall [Canada]

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Canada/Ottawa: Logo - Viande Richelieu Inc.Viande Richelieu Inc., a Massueville, Quebec establishment, recalls certain batch/lots of Viande Richelieu Meat branded Boneless Horse Meat products from the Canadian marketplace due to suspected presence of Clenbuterol, a steroid-like chemical initially developed to treat Asthma in horses and consequential risks of heart palpitations, atrial fibrillation or an irregular and often fast heartbeat and problems with blood pressure in humans, all serious health hazards.

CFIA: http://ht.ly/9mM030qaqbw

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/inspection/2020/72147r-eng.php

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

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Airome & Deep Soothe Essential Oil Recall [US]

Airome & Deep Soothe Essential Oil Recall [US]

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US FlagUS/Washington: B&B Acquisition, a Salt Lake City, Utah establishment, recalls an estimated 62,700 Airome branded Wintergreen Essential Oil and Deep Soothe branded Essential Oil 100 percent Pure & Natural Therapeutic Grade Essential Oils due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risk of poisoning, ingestion and GI tract laceration damage, all serious health hazards.

CPSC: http://ht.ly/YpRK30pVmDO

Direct link: https://www.cpsc.gov/Recalls/2020/BB-Acquisition-Recalls-Wintergreen-Essential-Oils-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Wintergreen Essential Oil products.

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Alocane Emergency Burn Pad Recall [US]

US FlagUS/Washington: Alocane Emergency Burn Pad Recall [US]Quest Products LLC, a Pleasant Prairie, Wisconsin establishment, recalls an estimated 153,000 Alocane Emergency Burn Pads due to suspected failure to meet US Child Resistant Closure requirements with consequential risks of chemical ingestion and poisoning, all serious health and safety hazards.

CPSC: http://ht.ly/vb9430pUtQ2

Direct link: https://www.cpsc.gov/Recalls/2020/Quest-Products-Recalls-ALOCANE-Emergency-Burn-Pads-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 Alocane branded Emergency Burn Pads (10 count and 15 count) that come in a white and red box with the phrase, “Maximum Strength Alocane Emergency Burn Pads” printed on the front.

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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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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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