D-1082-2019 Class III Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- April 17, 2019
- Initiation Date
- March 22, 2019
- Termination Date
- February 27, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 167 vials
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.
Distribution Pattern
Nationwide within the United States
Code Information
Lot 190205@1, expiry 08/4/19