GlaxoSmithKline recalls Tivicay 50mg tablets with incorrect expiration date labels (Jan 2027 instead of Sep 2026). This affects prescription bottles sold in the US. Check your label for lot number 2A9E.
Labeling: incorrect or missing lot and/or expiration date. An incorrect expiration date was printed on the product labeling with an expiration date of January 2027, whereas the correct expiration date is September 2026.
GlaxoSmithKline is recalling Tivicay (dolutegravir) 50mg tablets due to incorrect expiration dates on labels. This could lead to medication safety issues if patients use expired products. The recall affects prescription bottles with specific lot numbers.
The product labels show an incorrect expiration date of January 2027 instead of the correct September 2026. This could cause confusion about when the medication expires, potentially leading to improper use if patients assume it's still safe after the incorrect date.
Prescription patients using Tivicay 50mg tablets with the lot number 2A9E. Those who have the specific expiration date printed as January 2027 instead of September 2026 are most at risk.
Check your Tivicay 50mg tablets for a label with lot number 2A9E and an expiration date of January 2027. The product was manufactured for ViiV Healthcare in RTP, NC.
Look for the lot number 2A9E and expiration date of January 2027 on the product label.
The product labels show an incorrect expiration date of January 2027 instead of the correct September 2026.
Check your label for lot number 2A9E and expiration date of January 2027. If you have this specific product, contact your pharmacy for guidance.
The recall record does not specify a remedy. You should check with your pharmacy for advice.
We’ve drafted a message you can send GlaxoSmithKline to request your refund or repair — edit it as you like.
Subject: Recall D-0896-2022 — GlaxoSmithKline GlaxoSmithKline Hello, I own a GlaxoSmithKline that is covered by recall D-0896-2022 from GlaxoSmithKline. 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.
