# FDA recall D-0729-2022

> **Drug Depot, Inc., dba APS Pharmacy** · Class II · drug recall initiated 2022-03-23.

## Product

(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy

## Reason for recall

Lack of sterility assurance.

## Distribution

Nationwide in the USA including Puerto Rico.

## Key facts

- **Recall number:** D-0729-2022
- **Recalling firm:** Drug Depot, Inc., dba APS Pharmacy
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-03-23
- **Report date:** 2022-04-06
- **Termination date:** 2023-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Palm Harbor, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0729-2022

## Citation

> AI Analytics. FDA recall D-0729-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0729-2022. Source: US FDA. Licensed CC0.

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