# FDA recall D-296-2013

> **Jubilant Cadista Pharmaceuticals Inc.** · Class II · drug recall initiated 2013-02-11.

## Product

Pantoprazole Sodium Delayed Release Tablets USP, 40 mg, 90 count bottles, Manufactured by Jubilant Life Sciences Ltd, Roorkee-247661 India ;Marketed by Jubilant Cadista Pharmaceuatical Inc Salisbury, MD 21801 NDC 59746-284-90

## Reason for recall

cGMP Deviations: Oral products were not manufactured in accordance with Good Manufacturing Practices.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-296-2013
- **Recalling firm:** Jubilant Cadista Pharmaceuticals Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-02-11
- **Report date:** 2013-05-08
- **Termination date:** 2013-12-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Salisbury, MD, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-296-2013

## Citation

> AI Analytics. FDA recall D-296-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-296-2013. Source: US FDA. Licensed CC0.

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