# FDA recall D-017-2014

> **Apotex Inc.** · Class II · drug recall initiated 2013-07-17.

## Product

Acyclovir Tablets USP 800 mg ,(NDC 60505-5307-1), Rx only,  Manufactured by Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for Apotex Corp.,Weston, Florida 33326.

## Reason for recall

Presence of Particulate Matter: Product from lot KF2199, may contain tablets with pieces of nitrile rubber glove embedded within the tablets.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-017-2014
- **Recalling firm:** Apotex Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-07-17
- **Report date:** 2013-12-04
- **Termination date:** 2014-08-04

- **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-017-2014

## Citation

> AI Analytics. FDA recall D-017-2014. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-017-2014. Source: US FDA. Licensed CC0.

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