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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Green Lumber Dietary Supplement Recall [US]

Green Lumber Dietary Supplement Recall [US]

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US FlagUS/Silver Spring: GL Holdings, a Newport Beach, California establishment, recalls numerous batch/lots of Green Lumber Dietary Supplement Capsules due to suspected undeclared Tadalafil, an existing FDA approved drug for certain medical conditions. The undeclared presence of this medication can pose a serious health and safety hazard for some people.

FDA: http://ht.ly/dBa430pLE8Y

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gl-holdings-issues-voluntary-worldwide-recall-green-lumber-products-due-presence-undeclared

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

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Healing Solutions Wintergreen Essential Oil Recall [US]

US FlagUS/Washington: 12034 - CPSC - Healing Solutions Wintergreen Essential Oil Recall [US]Healing Solutions LLC, a Phoenix, Arizona establishment recalls an estimated 32,000 Healing Solutions branded Wintergreen and Birch 100 percent Pure 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/kZ4M30pwd5X

Direct link: https://www.cpsc.gov/Recalls/2019/Healing-Solutions-Recalls-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 Healing Solutions branded Wintergreen Essential Oil products.

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Aurora Cannabis Dried Cannabis Recall [Canada]

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Canada/Ottawa: Logo - Aurora Cannabis Aurora Cannabis Enterprises Ltd., a Cremona, Alberta establishment, recalls an estimated 3060 units (one batch/lot) of Blue Dream Sativa Dried Cannabis due to suspected inaccurate THC labeling and consequential lack of drug potency, both serious health and safety hazards.

HCSC: http://ht.ly/DET930pvxTE

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70865r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Dried Cannabis products are subject to this recall:

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Major Pharmaceuticals Milk of Magnesia Recall [US]

Major Pharmaceuticals Milk of Magnesia Recall [US]

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US FlagUS/Silver Spring: Plastikon Healthcare, LLC, a Lawrence, Kansas establishment, recalls certain batch/lots of Major Pharmaceuticals branded Milk of Magnesia 2400 mg/30 mL Oral Osmotic Laxative products, due to suspected risk of high levels of unspecified aerobic bacterial contamination and consequential risk of bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/1TJq30pvqkQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/plastikon-healthcare-issues-voluntary-nationwide-recall-milk-magnesia-oral-suspension-2400-mg30-ml

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

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