FDA Drug recall D-262-2013
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA
- FDA Drug
- Class I
- terminated
- Published 2013-04-24
On 2013-04-24 the FDA classified a Class I recall of Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA by Hospira, citing non-Sterility: Confirmed customer complaint of product contaminated with mold.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-262-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-01-25 |
| Published | 2013-04-24 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
Product
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.
Reason
Non-Sterility: Confirmed customer complaint of product contaminated with mold.
Identifiers
| code_info | Lot #: 05-019-JT*, Exp 05/01/13; lot number * may be followed by 01, 90, or 91. |
|---|
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-262-2013%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.