Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.

FDA recall notice · announced April 17, 2019 · Auro Pharmacies Inc. Dba Central Drugs

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.

Reason for recall

Failed pH Specification: product does not meet pH label claim.

Notes

Distribution: Nationwide within the United States
Lot/code information: Lot 190205@1, expiry 08/4/19
Quantity: 167 vials
Status: Terminated
Products in this recall event:
- Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630. (D-1082-2019)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.