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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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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Artizen Oils Therapeutic Essential Oil Recall [US]

Pure & Natural Therapeutic Essential Oil Recall [US]

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US FlagUS/Washington: Artizen Oils LLC, a Denver, Colorado recalls an estimated 6,000 Artizen Oils Wintergreen and Birch 100 percent Pure & Natural Therapeutic Grade Essential Oil products 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/76wB30ptGMa

Direct link: https://www.cpsc.gov/Recalls/2019/Artizen-Oils-Recalls-Essential-Oils-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisonin

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall includes all one- and two-ounce clear glass bottles of Artizen Oils Wintergreen and Birch 100 percent Pure & Natural Therapeutic Grade Essential Oils purchased prior to April 15, 2019.

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Epic Business Wintergreen Essential Oil Recall [US]

Epic Business Wintergreen Essential Oil Recall [US]

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US FlagUS/Washington: Epic Business Services, a San Diego, California establishment, recalls an estimated 11,580 Wintergreen Essential Oil products 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/Jvze30pb018

Direct link: https://www.cpsc.gov/Recalls/2019/Wintergreen-Essential-Oil-Recalled-by-Epic-Business-Services-Due-to-Failure-to-Meet-Child-Resistant-Closure-Requirement-Risk-of-Poisoning-Recall-Alert

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

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DaVinci Labs Omega-3 1000 Recall [US]

DaVinci Labs Omega-3 1000 Recall [US]

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US FlagUS/Silver Spring: DaVinci Laboratories, a division of FoodScience Corporation, a Williston, Vermont establishment, recalls certain batch/lots of Omega-3 1000 that may be labeled as Dim Plex due to undeclared Anchovy Fish and Sardine Fish, both known allergens, sources of dietary intolerance and possible triggers of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/f0iR30p7twq

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/davinci-laboratories-issues-allergy-alert-undeclared-fish-allergen-omega-3-1000-product-lot-35532200

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

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