# FDA recall D-1211-2018

> **Hetero Labs, Ltd. - Unit III** · Class III · drug recall initiated 2018-09-12.

## Product

Fenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ, 08854, NDC 31722-596-90

## Reason for recall

Presence of Foreign Tablet/Capsule: A foreign identified as Valacyclovir tablet 500 mg was co-mingled in a bottle containing Fenofibrate Tablets, USP 145 mg.

## Distribution

Indiana and Louisiana

## Key facts

- **Recall number:** D-1211-2018
- **Recalling firm:** Hetero Labs, Ltd. - Unit III
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-09-12
- **Report date:** 2018-10-03
- **Termination date:** 2018-11-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hyderabad, India

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1211-2018

## Citation

> AI Analytics. FDA recall D-1211-2018. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/D-1211-2018. Source: US FDA. Licensed CC0.

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