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

Family Dollar Dietary Supplements Recall: Rodent Contamination Risk

Family Dollar recalls dietary supplements sold in Alabama, Arkansas, Louisiana, Mississippi, Missouri, and Tennessee from January 2021 due to potential rodent contamination in distribution centers. Consumers should check product labels and contact Family Dollar for details.

🇺🇸 FDA recall #F-0812-2022FoodFamily 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 is recalling dietary supplements sold in several states from January 2021 because rodents may have contaminated the products during distribution. This could lead to potential exposure to rodent pathogens or parasites. Read more at govinfonow.com/recall/13280-family-dollar-dietary-supplements-recall-rodent-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/13280-family-dollar-dietary-supplements-recall-rodent-contamination-risk · Updated October 4, 2026 · FDA enforcement record: FDA #F-0812-2022

Cite this page

“Family Dollar Dietary Supplements Recall: Rodent Contamination Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13280-family-dollar-dietary-supplements-recall-rodent-contamination-risk. Based on FDA recall #F-0812-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0812-2022%22&limit=1).

Why it’s dangerous

Rodents in the distribution center could have contaminated the supplements with pathogens, parasites, or other harmful substances. This poses a risk of potential exposure to rodent-borne illnesses through ingestion of contaminated products.

Who’s affected

People who purchased dietary supplements (vitamins, minerals, herbal supplements) from Family Dollar stores in Alabama, Arkansas, Louisiana, Mississippi, Missouri, or Tennessee between January 2021 and present are affected. Those with compromised immune systems or allergies to rodent-related substances may be at higher risk.

How to tell if you have this one

Check for dietary supplements purchased from Family Dollar stores in Alabama, Arkansas, Louisiana, Mississippi, Missouri, or Tennessee from January 1, 2021 onward. Look for product labels indicating the specific supplement type (vitamins, minerals, herbal supplements).

  • Brand
    Family Dollar
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee
Recall numberProduct, codes & lots
F-0810-2022Food products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee; All food products purchased from Family Dollar retail stores located in AL, AR, LA, MS, MO, and TN from January 1, 2021 to present
F-0812-2022Dietary supplements purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee, including but not limited to vitamins, herbal and mineral supplements; All dietary supplements purchased from Family Dollar retail stores located in AL, AR, LA, MS, MO, and TN from January 1, 2021 to present
Based on the official FDA remedy

What to do — step by step

  1. Check Product Labels

    Review the product label to confirm it was purchased from Family Dollar stores in Alabama, Arkansas, Louisiana, Mississippi, Missouri, or Tennessee between January 1, 2021 and present.

  2. Contact Family Dollar

    Reach out to Family Dollar directly for assistance with the recall or to get information about the product.

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 and 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 terminated this recall 2.4 years after the firm started it.

1. Firm started the recall: Feb 18, 202212. FDA classified it Class II: Mar 3, 202223. Published in FDA’s Enforcement Report: Mar 9, 202234. FDA terminated the recall: Jul 17, 2024420222024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury from this recall?

The recall is for potential exposure to rodent activity, which could lead to health risks like infections or parasites, but the hazard level is low risk as no specific injuries have been reported.

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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 #F-0812-2022 (February 18, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0812-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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