# FDA recall D-1432-2012

> **Cadence Pharmaceuticals** · Class II · drug recall initiated 2012-07-24.

## Product

OFIRMEV (acetaminophen) injection, 1000 mg/100 mL (10 mg/mL), 24-count Single Use 100 mL Vials per carton, Rx only, Manufactured for: Cadence Pharmaceuticals, Inc., San Diego, CA  92130, NDC 43825-102-01, UPC 3 43825 10201 7.

## Reason for recall

Presence of Particulate Matter: The firm initiated the recall due to visible presence of particulate matter.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1432-2012
- **Recalling firm:** Cadence Pharmaceuticals
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-07-24
- **Report date:** 2012-08-08
- **Termination date:** 2013-11-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1432-2012

## Citation

> AI Analytics. FDA recall D-1432-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1432-2012. Source: US FDA. Licensed CC0.

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