Normosol-M and 5% Dextrose — Class III drug recall D-0727-2016
Ongoing recall by Hospira Inc., reported 2016-03-02, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer report of an incorrect expiration date
| Recall number | D-0727-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2016-02-02 |
| Classified | 2016-02-24 |
| Reported by FDA | 2016-03-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | HK |
| Quantity | 10,778 bags |
| Reason classes | labeling |
| NDC | 00409-7965-09 |
| Lot numbers | 56-853-FW |
| Expiration dates | 2017-08-01 |
Product
Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7965-09, Barcode (01) 0 030409 796509 0.
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer report of an incorrect expiration date printed on the primary container labeled "01AUG1017" rather than "01AUG2017".
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-0727-2016. 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.