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Stop using now Drug recall · FDA · Published November 6, 2015

Glades Drugs Recalls Vitamin D3 Supplements Due to High Potency

Glades Drugs Inc. recalls Vitamin D3 supplements because they contain an extremely high level of vitamin D3. Check lot codes and expiration dates.

🇺🇸 FDA recall #D-0669-2016DrugGlades Drugs ›
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Contact the company

Recalling firmGlades Drugs Inc.109 S Lake Ave · Pahokee, FL 33476-1803
✎ GovInfoNow plain-language explainer

What happened, in plain English

Glades Drugs Inc. is recalling Vitamin Supplement (Vial) D3 products because they contain an extremely high level of vitamin D3 (Cholecalciferol). This product was distributed in New York and Georgia with an expiration date of February 20, 2016. The recall involves approximately 7,800 capsules across various lot codes. Read more at govinfonow.com/recall/43402-glades-drugs-inc-recalls-vitamin-supplement-vial-d3-cholecalciferol-vit.

Source Summary by GovInfoNow · govinfonow.com/recall/43402-glades-drugs-inc-recalls-vitamin-supplement-vial-d3-cholecalciferol-vit · Updated October 11, 2026 · FDA enforcement record: FDA #D-0669-2016

Cite this page

“Glades Drugs Recalls Vitamin D3 Supplements Due to High Potency.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43402-glades-drugs-inc-recalls-vitamin-supplement-vial-d3-cholecalciferol-vit. Based on FDA recall #D-0669-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0669-2016%22&limit=1).

Why it’s dangerous

The supplement contains an extremely high level of vitamin D3 (Cholecalciferol), which classifies it as a superpotent drug. Excessive intake of vitamin D can lead to serious health issues, including toxicity, though specific injury details are not listed in the record.

Who’s affected

Consumers in New York and Georgia who purchased Glades Drugs Vitamin D3 supplements between vials of 60, 120, or 180 counts. Individuals taking this specific supplement are at risk due to the excessive dosage.

How to tell if you have this one

Look for Glades Drugs Vitamin Supplement (Vial) D3 in vials containing 60, 120, or 180 capsules. Check the expiration date of 02/20/2016 and verify if your lot code matches one of the following: AICACABF@3, AICECABF@2, AJBFCABF@4, ABCCABF@4, AICACABF@5, AICECABF@3, AJBHCABF@2, ABCCABF@5, AICBCABF@1, AICECABF@4, AJCBCABF@1, ABGCABF@4, AICBCABF@2, AICECABF@5, JCBCABF@2, BACDCABF@5, AICBCABF@3, AICICABF@3, BAAGCABF@2, BADACABF@3, AICBCABF@4, AJADCABF@1, BAAICABF@1, BACCABF@3, AICECABF@1, AJBECABF@6, BABCCABF@2, or BBAECABF@5.

  • Brand
    Glades Drugs
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop using the supplement

    Discontinue use of the recalled Vitamin D3 supplements immediately due to the superpotent dosage.

  2. Check your lot code

    Compare the lot code on your vial against the list provided in the recall record to confirm if it is affected.

Where it went and when

Where it was distributed

Distributed in Georgia and New York.

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: yesNYRhode 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: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

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

States: Georgia, New York.

Recall timeline

FDA published this recall 4 months after the firm started it.

1. Firm started the recall: Nov 6, 201512. FDA classified it Class I: Feb 16, 201623. Published in FDA’s Enforcement Report: Feb 24, 2016320152016
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

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

✎ GovInfoNow

Questions people ask

What specific ingredients are in the recalled product?

The product contains cholecalciferol (vit D3), lipoic acid, ubiquinol, methylcobalamin, pyridoxine, methionine, inositol, and choline bitartrate USP.

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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-0669-2016 (November 6, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0669-2016 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