Family Dollar recalls 24-count Sudfedrine PE Max Strength tablets distributed between April 30 and June 10, 2022, due to improper storage temperature conditions.
CGMP Deviations: product held outside appropriate storage temperature conditions.
Family Dollar is recalling 24-count Sudfedrine PE Max Strength tablets sold between April 30 and June 10, 2022. The product was stored outside the required temperature range, which could affect its safety.
The product was stored outside the required temperature range, which could lead to improper drug stability. This might affect the medication's effectiveness or safety, but the recall does not specify a risk of serious injury.
People who purchased these Sudfedrine tablets from Family Dollar stores between April 30 and June 10, 2022. Those with medical conditions requiring this medication may be at higher risk.
Check for the 24-count Sudfedrine PE Max Strength tablets with SKU 916001 purchased from Family Dollar stores between April 30 and June 10, 2022.
Verify the product was purchased from Family Dollar stores between April 30 and June 10, 2022, with SKU 916001.
The recall is due to improper storage temperature conditions, which could affect the medication's stability, but the official notice does not specify a risk of serious injury.
Check for the 24-count Sudfedrine PE Max Strength tablets with SKU 916001 purchased from Family Dollar stores between April 30 and June 10, 2022.
The recall does not provide a specific remedy, so you should check with Family Dollar or the manufacturer 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-1455-2022 — Family Dollar Family Dollar Hello, I own a Family Dollar that is covered by recall D-1455-2022 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.
