# FDA recall D-0727-2016

> **Hospira Inc.** · Class III · drug recall initiated 2016-02-02.

## 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".

## Distribution

Nationwide and Hong Kong

## Key facts

- **Recall number:** D-0727-2016
- **Recalling firm:** Hospira Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2016-02-02
- **Report date:** 2016-03-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lake Forest, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0727-2016

## Citation

> AI Analytics. FDA recall D-0727-2016. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-0727-2016. Source: US FDA. Licensed CC0.

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