# FDA recall D-1363-2014

> **Legacy Pharmaceutical Packaging** · Class II · drug recall initiated 2014-04-09.

## Product

Pantoprazole Sodium, Delayed-release tablets, USP, 40 mg tablets, 100 (10x10) unit dose packages, Manufactured by Dr. Reddy's Laboratories Limited, India and Distributed by Major Pharmaceuticals, Livonia, MI --- NDC 0904-6235-61

## Reason for recall

Correct Labeled Product Miscart/Mispack: some cartons labeled as Pantoprazole Sodium Delayed-Release may contain correctly labeled blister cards of Lorazepam tablets

## Distribution

IN

## Key facts

- **Recall number:** D-1363-2014
- **Recalling firm:** Legacy Pharmaceutical Packaging
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-04-09
- **Report date:** 2014-06-18
- **Termination date:** 2017-01-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Earth City, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1363-2014

## Citation

> AI Analytics. FDA recall D-1363-2014. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/D-1363-2014. Source: US FDA. Licensed CC0.

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