FDAFDA · Food and drugs·Recall number D-0013-2015
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
Published October 15, 2014 · Recall initiated: September 30, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Foreign Substance: Truvada was found to contain small red silicone rubber particulates.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- TRUVADA
- Manufacturer
- Gilead Sciences, Inc.
- Distributor
- Nationwide
- Lot
- TRUVADA (NDA 21-752; NDC 61958-0701-1) Lot# 002808, Expiration Date: 31 December 2017
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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