# FDA recall D-1059-2014

> **Greenstone Llc** · Class III · drug recall initiated 2013-11-04.

## Product

Glipizide XL (glipizide) extended release tablets, 5 mg , 500 count bottles, Rx only, Distributed by: Greenstone Ltd., Peapack, NJ ---  NDC 59762-5032-2

## Reason for recall

Failed Dissolution Specification; the bulk lot yielded an out of specification result at the 8 hr timepoint, 18 month interval

## Distribution

US Nationwide (including PR)

## Key facts

- **Recall number:** D-1059-2014
- **Recalling firm:** Greenstone Llc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-11-04
- **Report date:** 2014-02-12
- **Termination date:** 2015-06-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Peapack, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1059-2014

## Citation

> AI Analytics. FDA recall D-1059-2014. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1059-2014. Source: US FDA. Licensed CC0.

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