Advanced Nutriceuticals Recalls GHRP Vials Due to Sterility Concerns
Advanced Nutriceuticals is recalling GHRP vials because production processes cannot assure sterility. The product was distributed in seven states.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class II, and the hazard involves a lack of assurance of sterility for a sterile product, which poses a significant risk of infection or serious injury.
Plain-English summary
Advanced Nutriceuticals, LLC is recalling GHRP, 2000 MCG/ML, 5 ML vials manufactured by The Guyer Institute of Molecular Medicine in Indianapolis, IN. The recall is due to concerns with production processes that cannot assure the sterility of products intended to be sterile.
The affected product is identified by Lot #1112202008 with an expiration date of 12/11/2020. The product was distributed in California, Colorado, Florida, Indiana, Kentucky, Ohio, and Texas.
Consumers who have this product should stop using it and contact Advanced Nutriceuticals, LLC for further instructions.
The recalled product
- Product
- GHRP, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
- Manufacturer
- Advanced Nutriceuticals, LLC
- Category
- Drug — Injectable
- Affected units
- 1
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot #1112202008
- Exp 12/11/2020
Distribution
Part of a larger recall action
This product is one of 17 recalled by Advanced Nutriceuticals, LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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