0 — Class I drug recall D-922-2013
Terminated recall by Hospira Inc., reported 2013-09-04, distributed nationwide. Presence of Particulate Matter; product may contain fibrous material
| Recall number | D-922-2013 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2012-08-31 |
| Classified | 2013-08-26 |
| Reported by FDA | 2013-09-04 |
| Terminated | 2015-05-28 |
| Distributed | Nationwide (US) |
| Quantity | 264,432 bags |
| Reason classes | specification failure |
| NDC | 00409-7984-23 |
| Lot numbers | 05-201-JT |
| Expiration dates | 2013-05-01 |
Product
0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
Reason for recall
Presence of Particulate Matter; product may contain fibrous material
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-922-2013. 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.