# FDA recall D-1419-2012

> **Hospira Inc.** · Class I · drug recall initiated 2012-04-17.

## Product

Morphine Sulfate Injection, USP,  4mg/mL, 1 mL fill in 2.5 mL Carpuject Cartridge Unit with Luer Lock, packaged 10 Carpujects/carton, CII, Rx only, Hospira, Inc., Lake Forest, IL  ---- NDC 0409-1258-30

## Reason for recall

Superpotent; Cartridges labeled to contain 1 mL found to contain 2.2 mL

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1419-2012
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-04-17
- **Report date:** 2012-07-25
- **Termination date:** 2015-05-29

- **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-1419-2012

## Citation

> AI Analytics. FDA recall D-1419-2012. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-1419-2012. Source: US FDA. Licensed CC0.

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