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
- Recalling Firm
- Auro Pharmacies Inc. DBA Central Drugs
- 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.
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