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APS Isomorph, iForce Nutrition Mass Gainz supplements - recalled due to allergens
3 years ago •source fda.gov
Recall notice
United States
Company name: Hi-Tech Pharmaceuticals, Inc.Brand name: APS Isomorph, iForce Nutrition Mass Gainz
Product recalled: Dietary supplements
Reason of the recall: Due to undeclared milk, wheat, soy, egg allergens
FDA Recall date: April 03, 2021
Recall details: 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 recalled because it contains undeclared eggs. People who have an allergy or severe sensitivity to specific type of allergen (milk, eggs, wheat & soy) run the risk of serious or life-threatening allergic reaction if they consume these products.
Check the link below to get the full list of recalled products. APS Nutrition Isomorph 28 and iForce Nutrition Mass Gainz Brown Sugar Maple Oatmeal Cookie was distributed throughout the United States through direct sales, online stores, retails stores, and 3rd party distribution.
No illnesses have been reported to date.
The recall was initiated after it was discovered that product containing milk, eggs, wheat & soy allergens was distributed in packaging that did not reveal the presence of these allergens. Subsequent investigation indicates the problem was caused by an oversight on the label design prior to printing.
Consumers who have purchased APS Nutrition Isomorph 28 and iForce Nutrition Mass Gainz Brown Sugar Maple Oatmeal Cookie are urged to return it to the place of purchase for a full refund. Consumers with questions may contact Hi-Tech Pharmaceuticals at 1-888-855-7919 Monday – Friday 9:00 am –7:00 pm EST.
Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hi-tech-pharmaceuticals-issues-allergy-alert-various-aps-isomorph-28-products-and-iforce-nutrition
Source: FDA