# FDA recall D-1118-2017

> **PD-Rx Pharmaceuticals, Inc.** · Class III · drug recall initiated 2017-08-11.

## Product

Phentermine Capsules, 15 mg,  a) 7-count bottle (NDC 55289-791-07), b) 14-count bottle ( NDC 55289-791-14), c) 21-count bottle (NDC 55289-791-21), d) 30-count bottle (NDC 55289-791-30), e) 60-count bottle (NDC 55289-791-60), Packaged by PD-Rx Pharmaceuticals, Incorporated, Oklahoma City, OK. 73127 Mfg: KVK-Tech, Inc. Newtown, PA 18940

## Reason for recall

Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at 30th month Room Temperature Retained Sample stabilities test .

## Distribution

Nationwide.

## Key facts

- **Recall number:** D-1118-2017
- **Recalling firm:** PD-Rx Pharmaceuticals, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-08-11
- **Report date:** 2017-08-30
- **Termination date:** 2020-01-29

- **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-1118-2017

## Citation

> AI Analytics. FDA recall D-1118-2017. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-1118-2017. Source: US FDA. Licensed CC0.

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