Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Truvada (200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate) tablets Recalled by Gilead Sciences, Inc. Due to Presence of Foreign Substance: Truvada was found to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Gilead Sciences, Inc. directly.
Affected Products
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
Quantity: 10,317 bottles
Why Was This Recalled?
Presence of Foreign Substance: Truvada was found to contain small red silicone rubber particulates.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Gilead Sciences, Inc.
Gilead Sciences, Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report