# FDA recall D-0129-2024

> **Golden State Medical Supply Inc.** · Class II · drug recall initiated 2023-11-10.

## Product

PAROXETINE tablets, USP, 20 mg, Packaged as a) 90-count bottle NDC 60429-735-90; b)1000-count bottle, NDC 60429-735-10; Rx Only, Manufactured by Apotex, Inc., Toronto, Ontario, Canada, M9L 1T9, Packaged by GSMS, Incorporated, Camarillo, CA 93012.

## Reason for recall

Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0129-2024
- **Recalling firm:** Golden State Medical Supply Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-11-10
- **Report date:** 2023-12-06
- **Termination date:** 2025-03-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Camarillo, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0129-2024

## Citation

> AI Analytics. FDA recall D-0129-2024. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/D-0129-2024. Source: US FDA. Licensed CC0.

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