FDA Drug recall D-0334-2015
0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11
- FDA Drug
- Class II
- terminated
- Published 2015-01-14
On 2015-01-14 the FDA classified a Class II recall of 0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11 by Hospira, citing lack of Assurance of Sterility: The product has the potential for solution to leak at the administrative port.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0334-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-22 |
| Published | 2015-01-14 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
Product
0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11
Reason
Lack of Assurance of Sterility: The product has the potential for solution to leak at the administrative port.
Identifiers
| code_info | Lot #: 42-306-C6 |
|---|
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-0334-2015%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.