Family Dollar recalls two arthritis pain relief products for improper storage conditions that may affect quality. Consumers should check SKUs 999839 and 914771 sold between April 30 and June 10, 2022.
CGMP Deviations: product held outside appropriate storage temperature conditions.
Family Dollar is recalling two arthritis pain relief products because they were stored at incorrect temperatures. This could affect product quality but does not pose a serious injury risk.
The products were stored outside the required temperature range during distribution, which may cause quality issues. However, this does not involve a risk of injury or serious health effects.
People who purchased the recalled arthritis pain relief capsules from Family Dollar stores between April 30 and June 10, 2022. Those most at risk are individuals using the products for pain relief.
Check for the SKUs 999839 (BC Arthritis Pain Fast Pain Relief 24ct) or 914771 (Good Sense Arthritis Caplet 24ct) on the product packaging. These items were sold at Family Dollar stores from April 30 to June 10, 2022.
Look for the SKUs 999839 or 914771 on the product packaging to confirm if it is recalled.
No, the recall is for quality issues due to improper storage, not a risk of serious injury.
Check for SKUs 999839 (BC Arthritis Pain Fast Pain Relief 24ct) or 914771 (Good Sense Arthritis Caplet 24ct) on the packaging, which were sold at Family Dollar stores between April 30 and June 10, 2022.
The recall record does not specify a return or disposal action, so no action is required beyond checking the product details.
We’ve drafted a message you can send Family Dollar to request your refund or repair — edit it as you like.
Subject: Recall D-1388-2022 — Family Dollar Family Dollar Hello, I own a Family Dollar that is covered by recall D-1388-2022 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.