Advanced Nutriceuticals Recalls DSIP Vials Due to Sterility Concerns
Advanced Nutriceuticals is recalling DSIP vials because production processes cannot assure sterility. The product was distributed to specific states.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. 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 product intended to be sterile, which poses a significant risk of infection or serious injury.
Plain-English summary
Advanced Nutriceuticals, LLC is recalling DSIP, 1000 MCG/ML, 5 ML vials. The recall is due to concerns with production processes that cannot assure the sterility of products intended to be sterile.
The affected product is Lot #1111202002 with an expiration date of 12/11/2020. The product was distributed in California, Colorado, Florida, Indiana, Kentucky, Ohio, and Texas. The Guyer Institute of Molecular Medicine in Indianapolis, IN is listed in the product description.
Consumers should stop using the recalled product and contact the recalling firm for further instructions.
The recalled product
- Product
- DSIP, 1000 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 #1111202002
- 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.
See all 17 products in this recall →Related recalls
Same manufacturer · Advanced Nutriceuticals, LLC
See all →- SeverePT-141 Injection Recalled Due to Sterility Assurance Concerns
FDA (Drugs) · 2020-12-23
- SevereFDA Recalls NANDROLONE Injections Due to Sterility Concerns
FDA (Drugs) · 2020-12-23
- SevereAdvanced Nutriceuticals Recalls GHRP Vials Due to Sterility Concerns
FDA (Drugs) · 2020-12-23
- SevereFDA Recalls Cerebrolysin Vials Due to Sterility Concerns
FDA (Drugs) · 2020-12-23
- SevereFDA Recalls Thymosin Beta-4 Vials Due to Sterility Concerns
FDA (Drugs) · 2020-12-23
Same hazard · sterility
See all →- SevereK.C. Pharmaceuticals Recalls Target Eye Drops for Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereFDA Recalls Tri-MIX Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereFDA Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereFDA Recalls Tirzepatide Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereK.C. Pharmaceuticals Recalls Leader Advanced Relief Eye Drops for Sterility Concerns
FDA (Drugs) · 2026-10-14
Similar recalls
- SevereAdvanced Compounding Pharmacy Recalls Injectable Glutathione Due to Sterility Concerns
FDA (Drugs) · 2015-06-03
- ModerateAdvanced Pharma Recalls NitroGlycerin Syringes Due to Stability Data Issues
FDA (Drugs) · 2017-12-27
- SevereAdvanced Physician Solutions Recalls DMSO Injectable Vials Due to Sterility Concerns
FDA (Drugs) · 2015-06-03
- SevereAdvanced Physician Solutions Recalls Estradiol Cypionate Injectable Due to Sterility Concerns
FDA (Drugs) · 2015-06-03
- SevereAdvanced Pharma Recalls Glycopyrrolate Injectable Syringes Due to Sterility Concerns
FDA (Drugs) · 2019-03-27
- SevereAdvanced Physician Solutions Recalls Nanpyridoxine Injectable Due to Sterility Concerns
FDA (Drugs) · 2015-06-03