Atripla recall: Particulate Matter
Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil fumarate 300 mg) Tablets, 30 Tablet Bottles, Rx only. Manufactured for…
Why was Atripla recalled?
Presence of Foreign Substance: Red Silicone Rubber Particulates are Present in Drug.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #'s: 002390, 002400, Exp 02/17.
- Product
- Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil fumarate 300 mg) Tablets, 30 Tablet Bottles, Rx only. Manufactured for…
- Recalling firm
- Gilead Sciences, Inc.
- Quantity
- 39,223 bottles
- Distribution
- Nationwide including Puerto Rico.
- Recall date
- March 5, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)