Ceftazidime 2 gm / NS 50mL — Class II drug recall D-1201-2015
Terminated recall by Lincare, Inc., reported 2015-07-08, distributed in AR. Lack of Assurance of Sterility: Sterility of product is not assured.
| Recall number | D-1201-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lincare, Inc., Little Rock, AR, United States |
| Recall initiated | 2015-05-28 |
| Classified | 2015-07-01 |
| Reported by FDA | 2015-07-08 |
| Terminated | 2017-02-16 |
| Distributed | AR |
| Quantity | 15 bags |
| Reason classes | sterility |
Product
Ceftazidime 2 gm / NS 50mL, Qty: 15 50 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
Reason for recall
Lack of Assurance of Sterility: Sterility of product is not assured.
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-1201-2015. 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.