# FDA recall D-0013-2015

> **Gilead Sciences, Inc.** · Class III · drug recall initiated 2014-09-30.

## Product

Truvada (200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate) tablets, 30 count bottles, Rx only, Manufactured for Gilead Sciences, Inc. Foster City, CA 94404, NDC 61958-0701-1

## Reason for recall

Presence of Foreign Substance: Truvada was found to contain small red silicone rubber particulates.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0013-2015
- **Recalling firm:** Gilead Sciences, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-09-30
- **Report date:** 2014-10-15
- **Termination date:** 2015-05-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Foster City, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0013-2015

## Citation

> AI Analytics. FDA recall D-0013-2015. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0013-2015. Source: US FDA. Licensed CC0.

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