# FDA recall D-1522-2019

> **Geritrex, LLC** · Class II · drug recall initiated 2019-05-31.

## Product

Gericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg/5mL, 16 FL OZ (473 ml), Dist. BY: Gericare Pharmaceuticals corp. 1650 63rd Street Brooklyn, NY 11204, NDC 57896-403-16

## Reason for recall

cGMP Deviations: Products may have microbial contamination.

## Distribution

U.S.A. Nationwide

## Key facts

- **Recall number:** D-1522-2019
- **Recalling firm:** Geritrex, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-05-31
- **Report date:** 2019-07-31
- **Termination date:** 2024-02-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Middletown, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1522-2019

## Citation

> AI Analytics. FDA recall D-1522-2019. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-1522-2019. Source: US FDA. Licensed CC0.

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