FDA Drug recall D-0324-2015
HEPARIN SODIUM, 1000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500 mL flexible container unit,…
- FDA Drug
- Class I
- terminated
- Published 2014-12-31
On 2014-12-31 the FDA classified a Class I recall of HEPARIN SODIUM, 1000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500 mL flexible container unit,… by Hospira, citing presence of Particulate Matter: A particulate, confirmed as human hair, was found sealed between the tube and film at the round seal of the unused administrative port of the conta….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0324-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-09-11 |
| Published | 2014-12-31 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
Product
HEPARIN SODIUM, 1000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500 mL flexible container unit, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7620-03
Reason
Presence of Particulate Matter: A particulate, confirmed as human hair, was found sealed between the tube and film at the round seal of the unused administrative port of the container.
Identifiers
| ndc | 0409-7620-13 |
|---|---|
| ndc | 0409-7620-03 |
| ndc | 0409-7620-49 |
| ndc | 0409-7620-59 |
| ndc | 0409-1005-01 |
| ndc | 0409-1005-20 |
| ndc | 0409-2222-01 |
| ndc | 0409-2222-12 |
| code_info | Lot #: 41-046-JT, Exp 11/01/2015 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0324-2015%22
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