Biotin 10 mg/mL Injection recall
Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
Why was Biotin 10 mg/mL Injection recalled?
Failed pH Specification: product does not meet pH label claim.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot 190205@1, expiry 08/4/19
- Product
- Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
- Recalling firm
- Auro Pharmacies Inc. DBA Central Drugs
- Quantity
- 167 vials
- Distribution
- Nationwide within the United States
- Recall date
- April 17, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)