# FDA recall D-0559-2016

> **PD-Rx Pharmaceuticals, Inc.** · Class II · drug recall initiated 2015-07-10.

## Product

Clonidine Hydrochloride Tablets, USP, 0.1 mg, 100-count bottles, Rx only, Packaged by PD-RX Pharmaceuticals, Inc., Oklahoma City, OK 73127, MFG: Mutual Pharm. Co. Inc., Philadelphia, PA 19124, NDC 43063-509-01

## Reason for recall

cGMP Deviations

## Distribution

Alabama

## Key facts

- **Recall number:** D-0559-2016
- **Recalling firm:** PD-Rx Pharmaceuticals, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-07-10
- **Report date:** 2016-01-06
- **Termination date:** 2017-03-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oklahoma City, OK, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0559-2016

## Citation

> AI Analytics. FDA recall D-0559-2016. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0559-2016. Source: US FDA. Licensed CC0.

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