Vancomycin Hydrochloride for Injection — Class II drug recall D-0574-2020
Terminated recall by AuroMedics Pharma LLC, reported 2019-12-18, distributed nationwide. Discoloration: Product complaints of discoloration after reconstitution of vials.
| Recall number | D-0574-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AuroMedics Pharma LLC, East Windsor, NJ, United States |
| Recall initiated | 2019-11-25 |
| Classified | 2019-12-06 |
| Reported by FDA | 2019-12-18 |
| Terminated | 2021-03-04 |
| Distributed | Nationwide (US) |
| Quantity | 275,060 vials |
| NDC | 55150-0203, 55150-0203-10, 55150-0204, 55150-0204-20 |
| Lot numbers | CVM180003, CVM180004, CVM180008, CVM180009, CVM180010, CVM180011, CVM180012 |
| Expiration dates | 2020-04, 2020-07, 2020-09 |
Product
Vancomycin Hydrochloride for Injection, USP, 1 g* per vial, packaged in 10-count vials per carton, Rx only, Mft. in India for: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-204-20.
Reason for recall
Discoloration: Product complaints of discoloration after reconstitution of vials.
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-0574-2020. 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.