Ceftriaxone for Injection — Class III drug recall D-0145-2017
Terminated recall by Sandoz Inc, reported 2016-11-30, distributed in WI. Labeling: Missing Label
| Recall number | D-0145-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sandoz Inc, Princeton, NJ, United States |
| Recall initiated | 2016-10-19 |
| Classified | 2016-11-19 |
| Reported by FDA | 2016-11-30 |
| Terminated | 2017-07-27 |
| Distributed | WI |
| Quantity | 139,430 vials |
| Reason classes | labeling |
| NDC | 00409-7332, 00409-7332-01, 00409-7332-11, 00409-7335, 00409-7335-03, 00409-7335-13, 00409-7337, 00409-7337-01, 00409-7337-11, 00409-7338, 00409-7338-01, 00409-7338-11 |
| Lot numbers | 670028M, GJ7151 |
Product
Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH for Hospira Worldwide, Inc., Lake Forest, Il 60045, USA, Made in Austria, NDC 0409-7332-01
Reason for recall
Labeling: Missing Label
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-0145-2017. 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.