FDA Drug recall D-169-2013
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
- FDA Drug
- Class II
- terminated
- Published 2013-03-06
On 2013-03-06 the FDA classified a Class II recall of Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04 by Hospira, citing lack of Assurance of Sterility; possible loose crimp applied to fliptop vial.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-169-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-01-10 |
| Published | 2013-03-06 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
Product
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
Reason
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
Identifiers
| ndc | 0409-6102-19 |
|---|---|
| ndc | 0409-6102-02 |
| ndc | 0409-6102-18 |
| ndc | 0409-6102-04 |
| ndc | 0409-6102-20 |
| ndc | 0409-6102-10 |
| code_info | 18-099-DK |
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-169-2013%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.