Vancomycin Hydrochloride for Injection — Class II drug recall D-1033-2016
Terminated recall by Hospira Inc., reported 2016-06-22, distributed nationwide. Presence of Particulate Matter: Cardboard
| Recall number | D-1033-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2016-05-06 |
| Classified | 2016-06-15 |
| Reported by FDA | 2016-06-22 |
| Terminated | 2018-09-24 |
| Distributed | Nationwide (US) |
| Reason classes | specification failure |
| NDC | 00409-6510-01 |
| Lot numbers | 565003A |
| Expiration dates | 2017-08-01 |
Product
Vancomycin Hydrochloride for Injection, USP, 10 g, 100 mL vial, Rx only, Hospira, Lake Forest, IL, NDC 0409-6510-01
Reason for recall
Presence of Particulate Matter: Cardboard
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-1033-2016. 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.