Vancomycin Hydrochloride for Injection recall: Particulate Matter
Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02
Why was Vancomycin Hydrochloride for Injection recalled?
Presence of Particulate Matter: glass particulate found in vial
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: 632153A; Exp. 03/18
- Product
- Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02
- Recalling firm
- Pfizer Inc.
- Quantity
- 102,500 vials
- Distribution
- Nationwide USA and Puerto Rico
- Recall date
- December 27, 2017
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)