FDA Drug recall D-263-2013
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible containers, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7929…
- 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 containers, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7929… by Hospira, citing non-Sterility: One confirmed customer report that product contained spore-like particulates, consistent with mold.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-263-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-10-05 |
| 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 containers, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7929-09.
Reason
Non-Sterility: One confirmed customer report that product contained spore-like particulates, consistent with mold.
Identifiers
| code_info | Lot # :12-160-JT*, Exp 12/01/13; 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-263-2013%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.