FDA Drug recall D-1179-2017
Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs (NDC 0781-3407-95), R…
- FDA Drug
- Class III
- terminated
- Published 2017-10-04
On 2017-10-04 the FDA classified a Class III recall of Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs (NDC 0781-3407-95), R… by Sandoz, citing labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1179-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-09-25 |
| Published | 2017-10-04 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Sandoz |
| Distribution | US |
Product
Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs (NDC 0781-3407-95), Rx only, Manufactured in Austria by Sandoz GmbH or Sandoz Inc., Princeton, NJ 08540.
Reason
Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
Identifiers
| ndc | 0781-3400-78 |
|---|---|
| ndc | 0781-3400-95 |
| ndc | 0781-3402-78 |
| ndc | 0781-3402-95 |
| ndc | 0781-3407-78 |
| ndc | 0781-3407-95 |
| ndc | 0781-3404-85 |
| ndc | 0781-3404-95 |
| ndc | 0781-3408-80 |
| ndc | 0781-3408-95 |
| code_info | Lot: GH8254, Exp 06/19 |
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-1179-2017%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.