# FDA recall D-1081-2015

> **Apotex Inc.** · Class III · drug recall initiated 2015-04-07.

## Product

Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9

## Reason for recall

Subpotent drug

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1081-2015
- **Recalling firm:** Apotex Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-04-07
- **Report date:** 2015-05-20
- **Termination date:** 2017-04-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Toronto, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1081-2015

## Citation

> AI Analytics. FDA recall D-1081-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1081-2015. Source: US FDA. Licensed CC0.

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