Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Trizivir (abacavir sulfate 300mg Recalled by GlaxoSmithKline Inc Due to Adulterated Presence of Foreign Tablets: Trizivir 300/150/300 mg...
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 GlaxoSmithKline Inc directly.
Affected Products
Trizivir (abacavir sulfate 300mg, lamivudine 150 mg and zidovudine 300 mg), 60 Tablets, Rx only, Manufactured for: ViiV Healthcare, Research Triangle Park, NC 27709 by: GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 49702-217-18
Quantity: 14,465 bottles
Why Was This Recalled?
Adulterated Presence of Foreign Tablets: Trizivir 300/150/300 mg tables, Lot 0ZP5128 may incorrectly contain Lexiva 700 mg tablets.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GlaxoSmithKline Inc
GlaxoSmithKline Inc has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report