# FDA recall D-1437-2019

> **Geritrex, LLC** · Class II · drug recall initiated 2019-05-06.

## Product

Senna (sennosides 8.8 mg) Syrup 8 fl oz. (236 mL) bottles, Distributed by Geritrex, LLC 40 Commercial Avenue Middletown, NY 10941, NDC 54162-007-08

## Reason for recall

Failed Impurities/Degradation Specifications: Atypical odor and unpleasant taste was reported

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-1437-2019
- **Recalling firm:** Geritrex, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-05-06
- **Report date:** 2019-06-19
- **Termination date:** 2024-02-21

- **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-1437-2019

## Citation

> AI Analytics. FDA recall D-1437-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-1437-2019. Source: US FDA. Licensed CC0.

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