# FDA recall D-0276-2022

> **Ascent Pharmaceuticals, Inc.** · Class II · drug recall initiated 2021-11-19.

## Product

Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg, 100-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY 11722, NDC 31722-997-01.

## Reason for recall

Product Mix-up

## Distribution

USA Nationwide

## Key facts

- **Recall number:** D-0276-2022
- **Recalling firm:** Ascent Pharmaceuticals, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-11-19
- **Report date:** 2021-12-15
- **Termination date:** 2023-12-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Central Islip, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0276-2022

## Citation

> AI Analytics. FDA recall D-0276-2022. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/D-0276-2022. Source: US FDA. Licensed CC0.

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