# FDA recall D-1570-2014

> **Apotex Corp.** · Class III · drug recall initiated 2014-08-21.

## Product

Candesartan Cilexetil and Hydrochlorothiazide Tablets 32 mg/12.5 mg, 90 count bottles, Rx only, Manufactured by: Apotex Research Pvt. Ltd. Bangalore - 560 099, India NDC 60505-3759-9

## Reason for recall

Failed Impurity/Degradation Specification; high out of specification for CAD II degradant

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1570-2014
- **Recalling firm:** Apotex Corp.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-08-21
- **Report date:** 2014-09-24
- **Termination date:** 2019-10-02

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1570-2014

## Citation

> AI Analytics. FDA recall D-1570-2014. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1570-2014. Source: US FDA. Licensed CC0.

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