Epicure Recalls Glass Prep Bowls Due to Laceration Hazard

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The tempered glass bowl can break or shatter during use, posing a laceration hazard.

Source: Recall List

RH Recalls Children’s Bath Wraps Due to Violation of Federal Flammability Standard

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The recalled bath wraps fail to meet flammability standards for children’s sleepwear, posing a risk of burn injuries to children.

Source: Recall List

Yolo Studio Issues Voluntary Nationwide Recall of PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 Due to the Presence of Undeclared Tadalafil

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Cliffside Park, NJ, Yolo Studio is voluntarily recalling all lots of PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500 to the consumer level. FDA analysis has found the product to contain undeclared tadalafil. Tadalafil is ingredient known as a phosphodiesterase (PDE-5) in

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

Yolo Studio Issues Voluntary Nationwide Recall of PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500 Due to the Presence of Undeclared Tadalafil

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Cliffside Park, NJ, Yolo Studio is voluntarily recalling all lots of PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500 to the consumer level. FDA analysis has found the product to contain undeclared tadalafil. Tadalafil is ingredient known as a phosphodiesterase (PDE-5) in

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

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 in 4.85lb jugs and 10 lb bags is also being reca

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. See the photo below. This recall is being con

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

Infant Bath Seats Recalled Due to Drowning Hazard; Imported by BATTOP; Sold Exclusively on Amazon.com (Recall Alert)

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The bath seats fail to meet the federal safety standard for infant bath seats, including requirements for stability, and can tip over while in use, posing a drowning hazard to babies.

Source: Recall List

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 contents are applied to the skin or swallowed by young children.

Source: Recall List