Entries by Heather Davis

HI-TECH Pharmaceuticals Issues Allergy Alert on Various APS Isomorph 28 Products and iFORCE Nutrition Mass Gainz Dietary Supplements Due to Possible Undeclared Milk, Eggs, Wheat and Soy

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Hi-Tech Pharmaceuticals. Inc. of Norcross, GA is recalling all lots of APS Nutrition Isomorph 28 flavors in a 2 lb jug because it contains undeclared milk, wheat & soy allergens. All lots of iForce Nutrition Mass Gainz Brown Sugar Maple Oatmeal Cookie ...

Source: Food and Drugs Administration--Recalls/Safety Alerts

A-S Medication Solutions Issues Voluntary Nationwide Recall of Acetaminophen Extra Strength Tablets Contained in Health Essentials Kits Due to Mislabeling

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Libertyville, IL, A-S Medication Solutions, LLM (ASM) is voluntarily recalling 198,350 bottles of Acetaminophen Extra Strength 500 mg Tablets, 100 ct. bottles (NDC# 50090-5350-0) contained in Health Essentials Kits distributed by Humana to its members....

Source: Food and Drugs Administration--Recalls/Safety Alerts

dōTERRA Recalls 1.3 Million Bottles of Deep Blue, PastTense, and Deep Blue Touch Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

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The products contain the substance methyl salicylate, which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA).  The packaging of the products is not child resistant, posing a risk of poisoning if the co...

Source: Recall List

QMART Issues Voluntary Nationwide Recall of IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 Due to Presence of Undeclared Sildenafil and/or Tadalafil

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Elmwood Park, NJ, QMART is voluntarily recalling all lots of IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 to the consumer level. FDA analysis has found the products to be tainted with undeclared sildena...

Source: Food and Drugs Administration--Recalls/Safety Alerts

Apotex Corp. Issues Voluntary Nationwide Recall of Guanfacine Extended-Release Tablets 2mg Due to Trace Amounts of Quetiapine Fumarate

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Weston, Florida, Apotex Corp is voluntarily recalling three (3) lots of Guanfacine Extended-Release Tablets 2mg to the consumer level due to trace amounts of Quetiapine Fumarate in one lot RX1663. Out of an abundance of caution, lots RX1662 and RX1664 ...

Source: Food and Drugs Administration--Recalls/Safety Alerts

NANA Collection LLC Issues Voluntary Nationwide Recall of PremierZen Platinum 5000 & Triple SupremeZen Gold 3500 Due to Presence of Undeclared Drug Tadalafil and Sildenafil

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NANA Collection LLC is voluntarily recalling all lots of PremierZen Platinum 5000 and Triple SupremeZen Gold 3500 to the consumer level. FDA analysis has found the PremierZen Platinum 5000 to contain undeclared Tadalafil and Triple SupremeZen 3500 to c...

Source: Food and Drugs Administration--Recalls/Safety Alerts

Ummzy LLC Issues Voluntary Nationwide Recall of Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night Due to the Presence of Undeclared Tadalafil Sildenafil & Vardenafil

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Palisades Park, NJ, Ummzy LLC is voluntarily recalling all lots of Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Nightcapsules to consumer level. FDA analysis has found the product to contain undeclared tadalafil sildenafil & Vardenafil. Tadalafil, ...

Source: Food and Drugs Administration--Recalls/Safety Alerts

Nuri Trading LLC Issues Voluntary Nationwide Recall of Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, 69MODE Blue 69, Due to the Presence of Undeclared Tadalafil, Sildenafil, and/ or Vardenafil

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Nuri Trading is voluntarily recalling all lots within expiry of Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, and 69MODE Blue 69 capsules to the consumer level.FDA analyses have found these products to contain undeclared tadalafil, s...

Source: Food and Drugs Administration--Recalls/Safety Alerts