Family Dollar recalls 100-count DRX Fiber Capsules distributed between April 30 and June 10, 2022, due to improper storage temperatures affecting product safety.
CGMP Deviations: product held outside appropriate storage temperature conditions.
Family Dollar is recalling 100-count DRX Fiber Capsules sold between April 30 and June 10, 2022. The capsules were stored at incorrect temperatures, which could affect their safety and effectiveness.
The capsules were stored outside the proper temperature range, which could lead to reduced effectiveness or potential safety issues. This is a manufacturing issue related to storage conditions during production.
Customers who purchased DRX Fiber Capsules from Family Dollar Stores between April 30 and June 10, 2022. People taking these capsules regularly are most at risk if the product was stored improperly.
Check for DRX Fiber Capsules 100-count with SKU 998899 purchased from Family Dollar Stores between April 30 and June 10, 2022.
Verify the product was purchased between April 30 and June 10, 2022, from Family Dollar Stores with SKU 998899.
The product was stored outside the appropriate temperature conditions during distribution, which could affect its safety and effectiveness.
Check for DRX Fiber Capsules 100-count with SKU 998899 purchased from Family Dollar Stores between April 30 and June 10, 2022.
The recall does not specify a remedy, so you should check with Family Dollar Stores for further instructions.
We’ve drafted a message you can send Family Dollar to request your refund or repair — edit it as you like.
Subject: Recall D-1423-2022 — Family Dollar Family Dollar Hello, I own a Family Dollar that is covered by recall D-1423-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
