Vancomycin Hydrochloride for Injection recall: Particulate Matter
Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials per carton, Rx only, Distributed by: Hospira, Inc., Lake Forest, IL 60045. NDC Vial 0409-3515-11; NDC Carton 0409-3515-01
Why was Vancomycin Hydrochloride for Injection recalled?
Presence of Particulate Matter: Glass particulate matter detected in injectable.
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: 33045BA, EXP 1SEP2023
- Product
- Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials per carton, Rx only, Distributed by: Hospira, Inc., Lake Forest, IL 60045. NDC Vial 0409-3515-11; NDC Carton 0409-3515-01
- Recalling firm
- Pfizer Inc.
- Quantity
- 89,700 vials
- Distribution
- USA nationwide and Puerto Rico
- Recall date
- February 1, 2023
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)