FDA Drug recall D-836-2013
0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09
- FDA Drug
- Class I
- terminated
- Published 2013-08-14
On 2013-08-14 the FDA classified a Class I recall of 0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09 by Hospira, citing presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-836-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-03-29 |
| Published | 2013-08-14 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
Product
0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
Reason
Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates
Identifiers
| code_info | Lot #: 25-037-JT*, Exp 1JAN2015, Note: the lot number may be followed by 01 or 90 |
|---|
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-836-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.