LACTATED RINGER'S and 5% DEXTROSE Injection USP — Class I drug recall D-0392-2015
Terminated recall by Hospira Inc., reported 2015-02-25, distributed nationwide. Non-Sterility: Confirmed customer complaint of particulate matter floating within the solution of the primary
| Recall number | D-0392-2015 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2014-07-10 |
| Classified | 2015-02-17 |
| Reported by FDA | 2015-02-25 |
| Terminated | 2015-11-23 |
| Distributed | Nationwide (US) |
| Quantity | 142,644 bags |
| Reason classes | microbial contamination, sterility, specification failure |
| Pathogens | mold |
| NDC | 00409-7929-09 |
| Lot numbers | 11/15, 35-118 |
Product
LACTATED RINGER'S and 5% DEXTROSE Injection USP, 1000 mL, flexible containers, Rx Only, Hospira, Inc., Lake Forest, IL 600045, NDC 0409-7929-09
Reason for recall
Non-Sterility: Confirmed customer complaint of particulate matter floating within the solution of the primary container, consistent with mold.
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-0392-2015. 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.