0 — Class I drug recall D-836-2013
Terminated recall by Hospira Inc., reported 2013-08-14, distributed nationwide. Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identifie
| Recall number | D-836-2013 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2013-03-29 |
| Classified | 2013-08-02 |
| Reported by FDA | 2013-08-14 |
| Terminated | 2015-07-20 |
| Distributed | Nationwide (US) |
| Quantity | 691,356 containers |
| Reason classes | specification failure |
| NDC | 00409-7983-09 |
| Expiration dates | 2015-01-01 |
Product
0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
Reason for recall
Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates
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-836-2013. 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.