PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: April 17, 2019 Initiated: March 22, 2019 #D-1082-2019

Product Description

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.

Details

Units Affected
167 vials
Distribution
Nationwide within the United States
Location
La Habra, CA

Frequently Asked Questions

What product was recalled?
Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.. Recalled by Auro Pharmacies Inc. DBA Central Drugs. Units affected: 167 vials.
Why was this product recalled?
Failed pH Specification: product does not meet pH label claim.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 17, 2019. Severity: Low. Recall number: D-1082-2019.