FDA Drug recall D-0145-2017
Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH for Hospira Worldwid…
- FDA Drug
- Class III
- terminated
- Published 2016-11-30
On 2016-11-30 the FDA classified a Class III recall of Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH for Hospira Worldwid… by Sandoz, citing labeling: Missing Label.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0145-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-10-19 |
| Published | 2016-11-30 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Sandoz |
| Distribution | WI |
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
Labeling: Missing Label
Identifiers
| ndc | 0409-7337-11 |
|---|---|
| ndc | 0409-7337-01 |
| ndc | 0409-7338-11 |
| ndc | 0409-7338-01 |
| ndc | 0409-7332-11 |
| ndc | 0409-7332-01 |
| ndc | 0409-7335-13 |
| ndc | 0409-7335-03 |
| code_info | Sandoz - Lot GJ7151(Pfizer- Lot 670028M); Exp. 07/19 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0145-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.