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Lower risk Drug recall · FDA · Published February 18, 2022

Family Dollar OTC Drugs Recall: Rodent Contamination Risk

Family Dollar stores in Alabama, Arkansas, Louisiana, Mississippi, Missouri, and Tennessee sold OTC drugs with potential rodent exposure. Consumers should check if their products were distributed between January 2021 and present.

🇺🇸 FDA recall #D-0641-2022DrugFamily Dollar ›
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Contact the company

Recalling firmDollar Tree Distribution, Inc.500 Volvo Pkwy · Chesapeake, VA 23320-1604
✎ GovInfoNow plain-language explainer

What happened, in plain English

Family Dollar stores in Alabama, Arkansas, Louisiana, Mississippi, Missouri, and Tennessee sold OTC drugs that may have been contaminated by rodents during distribution. This recall is due to potential exposure to rodents in the distribution center, which could pose a health risk. Read more at govinfonow.com/recall/35211-family-dollar-otc-drugs-recall-rodent-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/35211-family-dollar-otc-drugs-recall-rodent-contamination-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0641-2022

Cite this page

“Family Dollar OTC Drugs Recall: Rodent Contamination Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35211-family-dollar-otc-drugs-recall-rodent-contamination-risk. Based on FDA recall #D-0641-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0641-2022%22&limit=1).

Why it’s dangerous

Rodents in the distribution center could contaminate the drugs with their droppings, fur, or other materials. This poses a risk of exposure to pathogens or allergens that could cause illness or allergic reactions in sensitive individuals.

Who’s affected

People who purchased OTC drugs from Family Dollar stores in Alabama, Arkansas, Louisiana, Mississippi, Missouri, or Tennessee between January 2021 and present. Those most at risk are individuals with compromised immune systems or allergies to rodent-related materials.

How to tell if you have this one

Check if you bought OTC drugs from Family Dollar stores in Alabama, Arkansas, Louisiana, Mississippi, Missouri, or Tennessee between January 1, 2021 and the present date. The products were distributed through Family Dollar retail stores in those states.

  • Brand
    Family Dollar
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Review the product packaging for the distribution date and location to confirm if it matches the recall criteria.

Where it went and when

Where it was distributed

Distributed in 6 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Alabama, Arkansas, Louisiana, Mississippi, Missouri, Tennessee” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arkansas, Louisiana, Mississippi, Missouri, Tennessee.

Recall timeline

FDA published this recall 19 days after the firm started it.

1. Firm started the recall: Feb 18, 202212. FDA classified it Class II: Mar 1, 202223. Published in FDA’s Enforcement Report: Mar 9, 202232022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #D-0641-2022 (February 18, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0641-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA