LACTATED RINGER'S Injection — Class I drug recall D-1270-2020
Terminated recall by ICU Medical Inc, reported 2020-05-27, distributed nationwide. Presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified
| Recall number | D-1270-2020 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ICU Medical Inc, Lake Forest, IL, United States |
| Recall initiated | 2020-05-08 |
| Classified | 2020-05-19 |
| Reported by FDA | 2020-05-27 |
| Terminated | 2021-11-10 |
| Distributed | Nationwide (US) |
| Quantity | 93,648 flexible |
| Reason classes | specification failure |
| NDC | 00409-7953-09 |
| Lot numbers | 07-514-FW |
| Expiration dates | 2021-07-01 |
Product
LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
Reason for recall
Presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified as iron oxide.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1270-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.