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Use caution Food recall · FDA · Published January 22, 2019

Good Neighbor Pharmacy Co Q10 Recall: Mislabeled Vit D Risk

Good Neighbor Pharmacy recalls 5,484 bottles of Co Q10 200mg capsules due to mislabeling and potential Vitamin D contamination. Check your UPC.

🇺🇸 FDA recall #F-1146-2019FoodGood Neighbor Pharmacy ›
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Contact the company

Recalling firmTwenty-First Century Healthcare, Inc2119 S Wilson St · Tempe, AZ 85282-2034
✎ GovInfoNow plain-language explainer

Twenty-First Century Healthcare, Inc. is recalling Good Neighbor Pharmacy brand Co Q10 200mg dietary supplement capsules because the product is mislabeled and may contain Vitamin D 2000 IU. The recall affects 5,484 bottles distributed nationwide through distributors. Consumers should check their bottles for specific lot numbers to see if they are included in this recall. Read more at govinfonow.com/recall/17797-good-neighbor-pharmacy-co-q10-recall-mislabeled-vit-d-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/17797-good-neighbor-pharmacy-co-q10-recall-mislabeled-vit-d-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-1146-2019

Cite this page

“Good Neighbor Pharmacy Co Q10 Recall: Mislabeled Vit D Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/17797-good-neighbor-pharmacy-co-q10-recall-mislabeled-vit-d-risk. Based on FDA recall #F-1146-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1146-2019%22&limit=1).

The FDA announced on Jan. 22, 2019, that Twenty-First Century Healthcare, Inc. is recalling Good Neighbor Pharmacy Co Q10 200mg capsules due to mislabeling and potential Vitamin D contamination. Owners should stop using the product immediately.

How to tell if you have it

  • Good Neighbor Pharmacy, Co Q10 200mg Capsule, Dietary Supplement
  • UPC: 0-87701-40817-5
  • Lot Number: 12921101
  • Exp Date: 06/21
  • 30 capsules

The hazard

The product is mislabeled and may contain Vitamin D 2000 IU. The FDA classified the recall as Class III.

Context

GovInfoNow's records show Twenty-First Century Healthcare, Inc. has one other recall on record since May 7, 2021, involving mislabeled Vitamin D3 tablets. Other recent recalls of similar products include Winder Labs Grape Multivitamins (Oct. 27, 2025), Yunker Energy & Health Herbal Supplement (March 12, 2026), and Wellnov Liposomal Mens 50+ Liquid Multivitamin Drops (April 23, 2026).

How to tell if you have this one

Look for Good Neighbor Pharmacy brand Co Q10 200mg Capsule, Dietary Supplement in 30-capsule bottles. Check for UPC: 0-87701-40817-5 and Lot Number: 12921101 with an expiration date of 06/21.

  • Brand
    Good Neighbor Pharmacy
  • Product
    Good Neighbor Pharmacy, Co Q10 200mg Capsule, Dietary Supplement, UPC: 0-87701-40817-5, 30 capsules
  • 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 III
  • Status
    Terminated
  • Distribution
    Nationwide. 14 DCs and distributor. No foreign/VA/govt/military consignees.
Recall numberProduct, codes & lots
F-1146-2019Good Neighbor Pharmacy, Co Q10 200mg Capsule, Dietary Supplement, UPC: 0-87701-40817-5, 30 capsules.; Lot Number: 12921101 Exp Date: 06/21 Product Number: 0-87701-40817-5
F-1147-2019Good Neighbor Pharmacy, D 2000 IU, Dietary Supplement, UPC: 0-87701-40751-2, 30 tablets.; Lot Number: 12921101 Exp Date: 06/21 Product Number: 0-87701-40751-2
Based on the official FDA remedy

What to do — step by step

  1. Check your bottle details

    Verify if your bottle has UPC 0-87701-40817-5 and Lot Number 12921101 with an expiration date of 06/21.

  2. Contact the manufacturer

    Since no specific remedy is stated in the record, contact Twenty-First Century Healthcare, Inc. for further instructions on returns or refunds.

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. 14 DCs and distributor. No foreign/VA/govt/military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Jan 22, 201912. FDA classified it Class III: Mar 5, 201923. Published in FDA’s Enforcement Report: Mar 13, 201934. FDA terminated the recall: Aug 29, 201942019
  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.

✎ GovInfoNow

Questions people ask

How many bottles are affected by this recall?

A total of 5,484 bottles were distributed nationwide through 14 distribution centers and distributors.

Where was this product sold?

The product was distributed nationwide through 14 distribution centers and distributors; no foreign, VA, government, or military consignees were involved.

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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-1146-2019 (January 22, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1146-2019 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