Family Dollar recalls PREVACID 24HR LANSOPRAZOLE 15MG capsules sold between April 30 and June 10, 2022, due to potential storage temperature deviations affecting product safety.
CGMP Deviations: product held outside appropriate storage temperature conditions.
Family Dollar stores recalled PREVACID 24HR LANSOPRAZOLE 15MG capsules sold between April 30 and June 10, 2022. The recall is due to possible temperature issues during storage that could affect product safety.
The product may have been stored outside the proper temperature range, which could affect its safety and effectiveness. This is a manufacturing issue related to storage conditions during production or distribution.
People who purchased PREVACID 24HR LANSOPRAZOLE 15MG capsules from Family Dollar stores between April 30 and June 10, 2022. Those with the product are most at risk if it was stored outside recommended temperature conditions.
Check for PREVACID 24HR LANSOPRAZOLE 15MG capsules in 14-count bottles sold at Family Dollar stores between April 30 and June 10, 2022. The SKU number is 903449.
Look for the SKU number 903449 on the product packaging to confirm it was part of the recalled batch.
The recall is due to potential storage temperature deviations, but the product is safe if stored within the recommended temperature range.
Check for PREVACID 24HR LANSOPRAZOLE 15MG capsules in 14-count bottles sold at Family Dollar stores between April 30 and June 10, 2022. The SKU number is 903449.
The recall does not specify a remedy, so no action is required if the product was stored properly.
We’ve drafted a message you can send Family Dollar to request your refund or repair — edit it as you like.
Subject: Recall D-1420-2022 — Family Dollar Family Dollar Hello, I own a Family Dollar that is covered by recall D-1420-2022 from Family Dollar. 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.