Asegua recalls 28-tablet Sofosbuvir and Velpatasvir combination tablets due to blister packs not sealing properly, risking tablet exposure. Consumers should contact the manufacturer for details.
Defective Container: blister packs not properly sealed resulting in tablets being loose in the carton.
Asegua is recalling Sofosbuvir and Velpatasvir tablets because the blister packs may not seal correctly, causing tablets to become loose. This could lead to accidental exposure or contamination if the tablets are not properly protected.
The blister packs may not seal properly, allowing tablets to become loose in the carton. This could lead to accidental exposure or contamination if the tablets are not properly protected.
People with a prescription for Sofosbuvir and Velpatasvir tablets from Asegua Therapeutics LLC. Those who have the specific 28-tablet package with 2x14 blister cards are most at risk.
Check for the 28-tablet package with 2x14 blister cards labeled 'Sofosbuvir and Velpatasvir, 400 mg/100 mg', manufactured for Asegua Therapeutics LLC, with NDC# 72626-2701-1 and Lot# 24ASV002UA.
Verify the product has the NDC# 72626-2701-1 and Lot# 24ASV002UA to confirm it is part of the recall.
The recall is due to potential loose tablets in the blister packs, but the product is safe if stored properly. Consult the manufacturer for specific guidance.
Check for the 28-tablet package with 2x14 blister cards labeled 'Sofosbuvir and Velpatasvir, 400 mg/100 mg', manufactured for Asegua Therapeutics LLC, with NDC# 72626-2701-1 and Lot# 24ASV002UA.
The recall does not specify a remedy, so contact Asegua Therapeutics LLC directly for instructions.
We’ve drafted a message you can send Asegua to request your refund or repair — edit it as you like.
Subject: Recall D-0313-2025 — Asegua Asegua Hello, I own a Asegua that is covered by recall D-0313-2025 from Asegua. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
