# FDA recall D-020-2013

> **Hospira Inc.** · Class I · drug recall initiated 2012-08-15.

## Product

HYDROmorphone HCl Injection, USP, 2 mg/mL, 1 mL fill in a 2.5 mL Carpuject prefilled cartridge unit, packaged in 10-count Carpujects per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1312-30, Barcode (01) 1 030409 131230 9 (carton), (01) 0 030409 131230 2 (cartridge unit).

## Reason for recall

Superpotent (Single Ingredient) Drug: The prefilled cartridge unit has been found to be overfilled and contain more than the 1 mL labeled fill volume.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-020-2013
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-08-15
- **Report date:** 2012-10-31
- **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-020-2013

## Citation

> AI Analytics. FDA recall D-020-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-020-2013. Source: US FDA. Licensed CC0.

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