FDA Drug recall D-1036-2014
Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Rx only
- FDA Drug
- Class II
- terminated
- Published 2014-02-05
On 2014-02-05 the FDA classified a Class II recall of Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Rx only by Hospira, citing lack of Assurance of Sterility; potential leakage from administrative port.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1036-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-01-09 |
| Published | 2014-02-05 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
Product
Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Rx only. Hospira, Lake Forest, IL 60045. NDC 0409-7620-59.
Reason
Lack of Assurance of Sterility; potential leakage from administrative port.
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 #: 26-125-JT, Exp: 8/14 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1036-2014%22
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