Lactated Ringer's Injection — Class III drug recall D-215-2013
Terminated recall by Hospira, Inc., reported 2013-04-03, distributed in NC. CGMP Deviations: Shipment of product not approved for release.
| Recall number | D-215-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira, Inc., Lake Forest, IL, United States |
| Recall initiated | 2012-06-21 |
| Classified | 2013-03-22 |
| Reported by FDA | 2013-04-03 |
| Terminated | 2013-03-28 |
| Distributed | NC |
| Quantity | 1,296 units |
| Reason classes | cgmp, unapproved product |
| NDC | 00409-7953-09 |
| Lot numbers | 04/14, 16-836-FW |
Product
Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
Reason for recall
CGMP Deviations: Shipment of product not approved for release.
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-215-2013. 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.