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Stop using now Drug recall · FDA · Published November 6, 2018

Recall: Calcium Carbonate Antacid Tablets Contain Metal Particles

L. Perrigo Company recalls Healthy Accents, HealthMart, and DG health calcium carbonate chewable antacid tablets due to foreign metal particles.

🇺🇸 FDA recall #D-0266-2019DrugHealthy Accents / HealthMart / DG health ›
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Recalling firmL. Perrigo Company515 Eastern Ave · Allegan, MI 49010-9070
✎ GovInfoNow plain-language explainer

What happened, in plain English

L. Perrigo Company is recalling Calcium Carbonate chewable antacid tablets because they may contain metal particles. The affected products are sold under the Healthy Accents, HealthMart Pharmacy, and DG health brands. Consumers should check their bottles for specific lot numbers and expiration dates to see if they are included in this recall. Read more at govinfonow.com/recall/39439-recall-calcium-carbonate-antacid-tablets-contain-metal-particles.

Source Summary by GovInfoNow · govinfonow.com/recall/39439-recall-calcium-carbonate-antacid-tablets-contain-metal-particles · Updated October 11, 2026 · FDA enforcement record: FDA #D-0266-2019

Cite this page

“Recall: Calcium Carbonate Antacid Tablets Contain Metal Particles.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/39439-recall-calcium-carbonate-antacid-tablets-contain-metal-particles. Based on FDA recall #D-0266-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0266-2019%22&limit=1).

Why it’s dangerous

The product was found to contain metal particles, which is a foreign substance that could be swallowed. Ingesting metal particles can cause internal injury or other health complications.

Who’s affected

Consumers who purchased Calcium Carbonate chewable antacid tablets from the Healthy Accents, HealthMart Pharmacy, or DG health brands nationwide. Individuals with these specific lot numbers and expiration dates are at risk of ingesting foreign metal particles.

How to tell if you have this one

Check your bottle for the following details: Product is Calcium Carbonate chewable tablets, 750mg, in a 60-count bottle. Look for NDC numbers 55316-014-72 (Healthy Accents), 62011-0295-1 (HealthMart Pharmacy), or 55910-717-72 (DG health). Verify the lot numbers are PA17-412, PA17-077, PA17-196, PA17-127, or PA17-150, and that the expiration date is 11/18.

  • Brand
    Healthy Accents / HealthMart / DG health
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not consume the antacid tablets if they match the recalled lot numbers and expiration date.

  2. Check your bottle details

    Verify the NDC number, lot number, and expiration date against the recall list to confirm if your specific bottle is affected.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 23 months after the firm started it.

1. Firm started the recall: Nov 6, 201812. FDA classified it Class II: Nov 20, 201823. Published in FDA’s Enforcement Report: Nov 28, 201834. FDA terminated the recall: Sep 28, 2020420182020
  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.

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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-0266-2019 (November 6, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0266-2019 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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