Sterile powder Vancomycin Hydrochloride for Injection — Class III drug recall D-0254-2015
Terminated recall by Hospira Inc., reported 2014-11-26, distributed nationwide. Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.
| Recall number | D-0254-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2014-11-07 |
| Classified | 2014-11-19 |
| Reported by FDA | 2014-11-26 |
| Terminated | 2017-03-22 |
| Distributed | Nationwide (US) |
| Quantity | 316,640 vials |
| Reason classes | labeling |
| NDC | 00409-3515, 00409-3515-01, 00409-3515-11, 00409-4332, 00409-4332-01, 00409-4332-11, 00409-6531, 00409-6531-02, 00409-6531-12, 00409-6533, 00409-6533-01, 00409-6533-11, 00409-6533-21 |
| Lot numbers | 07/16, 08/16, 43-240-DD, 44-205-DD, 44-455-DD, 44-460-DD, 44-465-DD |
Product
Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira, Inc. Lake Forest, IL 60045, NDC 0409-6533-01.
Reason for recall
Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0254-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.