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Lower risk Food recall · FDA · Published March 27, 2018

Bestco Calcium Chews Have Lower Vitamin D Than Listed; Recalled

Bestco recalls Signature Care Calcium Chews due to incorrect Vitamin D labeling. The product contains 12.5 mcg (500 IU) instead of the declared 25 mcg (1000 IU) of Vitamin D. Consumers should check UPC code 0-21130-78686 and lot codes 7263AG6, 7282AG3, 7289AG1.

🇺🇸 FDA recall #F-1013-2018FoodBestco ›
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Recalling firmBestco, Inc.288 Mazeppa Rd · Mooresville, NC 28115-7928
✎ GovInfoNow plain-language explainer

What happened, in plain English

Bestco is recalling its Signature Care Calcium Chews because the product contains less Vitamin D than labeled. The bag says 25 mcg (1000 IU) but the actual amount is 12.5 mcg (500 IU). This could lead to insufficient Vitamin D intake for some users. Read more at govinfonow.com/recall/19485-bestco-calcium-chews-have-lower-vitamin-d-than-listed-recalled.

Source Summary by GovInfoNow · govinfonow.com/recall/19485-bestco-calcium-chews-have-lower-vitamin-d-than-listed-recalled · Updated October 7, 2026 · FDA enforcement record: FDA #F-1013-2018

Cite this page

“Bestco Calcium Chews Have Lower Vitamin D Than Listed; Recalled.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19485-bestco-calcium-chews-have-lower-vitamin-d-than-listed-recalled. Based on FDA recall #F-1013-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1013-2018%22&limit=1).

Why it’s dangerous

The product was labeled with 25 mcg (1000 IU) of Vitamin D per serving, but it actually contains only 12.5 mcg (500 IU). This means the product provides half the Vitamin D claimed, which could lead to insufficient Vitamin D intake for some users. The issue stems from a packaging revision error that did not update the batch records.

Who’s affected

People who own or use Bestco's Signature Care Calcium Chews with the UPC code 0-21130-78686 and lot codes 7263AG6, 7282AG3, or 7289AG1 are affected. Those who take the product for Vitamin D supplementation may be at risk of inadequate intake.

How to tell if you have this one

Check the UPC code 0-21130-78686 on the product packaging. The lot codes 7263AG6 (expires 09/2019), 7282AG3 (expires 10/2019), and 7289AG1 (expires 10/2019) are also associated with this recall.

  • Brand
    Bestco
  • Product
    Signature Care Calcium Chews; Dietary Supplement; 500 mg Calcium; 25 mcg Vitamin D; Chocolate; 100 chews; Serving Size
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC code 0-21130-78686 and lot codes 7263AG6, 7282AG3, or 7289AG1 on the packaging.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 5.5 years after the firm started it.

1. Firm started the recall: Mar 27, 201812. FDA classified it Class III: Apr 13, 201823. Published in FDA’s Enforcement Report: Apr 18, 201834. FDA terminated the recall: Oct 6, 2023420182023
  1. Firm started the recall
  2. FDA classified it Class III
  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.

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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-1013-2018 (March 27, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1013-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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