0 — Class II drug recall D-176-2013
Terminated recall by Hospira Inc., reported 2013-03-06, distributed nationwide. Lack of Assurance of Sterility: There is a potential for the solution to leak from the administration port of
| Recall number | D-176-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2013-02-12 |
| Classified | 2013-02-28 |
| Reported by FDA | 2013-03-06 |
| Terminated | 2015-04-24 |
| Distributed | Nationwide (US) |
| Quantity | 56,854 units |
| Reason classes | sterility, packaging |
| NDC | 00409-7972-08 |
Product
0.9% Sodium Chloride Irrigation, USP, 3000 mL, Sterile, Non pyrogenic, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7972-08
Reason for recall
Lack of Assurance of Sterility: There is a potential for the solution to leak from the administration port of the primary container.
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-176-2013. 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.