FDA Drug recall D-1270-2020
LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
- FDA Drug
- Class I
- terminated
- Published 2020-05-27
On 2020-05-27 the FDA classified a Class I recall of LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09 by Icu Medical, citing presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified as iron oxide.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1270-2020 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2020-05-08 |
| Published | 2020-05-27 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Icu Medical |
| Distribution | US |
Product
LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
Reason
Presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified as iron oxide.
Identifiers
| code_info | Lot #: 07-514-FW Exp. 01-JUL-2021 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1270-2020%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.