# FDA recall D-1226-2014

> **Hospira Inc.** · Class III · drug recall initiated 2014-03-25.

## Product

Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., Lake Forest, IL.

## Reason for recall

Labeling; Missing label; ampoules are missing the immediate container label

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1226-2014
- **Recalling firm:** Hospira Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-03-25
- **Report date:** 2014-04-16
- **Termination date:** 2015-12-18

- **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-1226-2014

## Citation

> AI Analytics. FDA recall D-1226-2014. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-1226-2014. Source: US FDA. Licensed CC0.

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