# FDA recall D-0272-2015

> **Perry Drug Inc.** · Class II · drug recall initiated 2014-11-07.

## Product

HCG-20,000 U/2 mL Vial, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS ---NDC 88888-2195-47

## Reason for recall

Lack of sterility assurance;All lots of sterile products compounded by the pharmacy that are within expiry were recalled due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

## Distribution

Kansas and Missouri

## Key facts

- **Recall number:** D-0272-2015
- **Recalling firm:** Perry Drug Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-11-07
- **Report date:** 2014-12-03
- **Termination date:** 2015-11-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Overland Park, KS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0272-2015

## Citation

> AI Analytics. FDA recall D-0272-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0272-2015. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
