0 — Class I drug recall D-0976-2015
Terminated recall by Hospira Inc., reported 2015-05-13, distributed nationwide. Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.
| Recall number | D-0976-2015 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2015-03-05 |
| Classified | 2015-05-04 |
| Reported by FDA | 2015-05-13 |
| Terminated | 2016-06-09 |
| Distributed | Nationwide (US) |
| Quantity | 9,912 visiv |
| Reason classes | specification failure |
| NDC | 00409-7983-25 |
| Lot numbers | 45-110-C6 |
| Expiration dates | 2016-03-01 |
Product
0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.
Reason for recall
Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.
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-0976-2015. 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.