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
Reported: October 15, 2014 Initiated: September 30, 2014 #D-0013-2015
Product Description
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.
Details
- Recalling Firm
- Gilead Sciences, Inc.
- Units Affected
- 10,317 bottles
- Distribution
- Nationwide
- Location
- Foster City, CA
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Gilead Sciences, Inc.. Units affected: 10,317 bottles.
Why was this product recalled? ▼
Presence of Foreign Substance: Truvada was found to contain small red silicone rubber particulates.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 15, 2014. Severity: Low. Recall number: D-0013-2015.
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