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Unrated Drug recall · FDA · Published November 23, 2016

Jeffreys Drug Store Recalls Domperidone Capsules 10mg Due to Unapproved Safety

Jeffreys Drug Store recalls 10mg domperidone capsules compounded in 60, 90, and 360-count bottles due to lack of FDA approval for safety and efficacy. Consumers should check lot numbers and expiration dates.

🇺🇸 FDA recall #D-0494-2017DrugJeffreys Drug Store ›
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Recalling firmJeffreys Drug Store1 N Central Ave · Canonsburg, PA 15317-1301
✎ GovInfoNow plain-language explainer

What happened, in plain English

Jeffreys Drug Store is recalling 10mg domperidone capsules compounded in 60, 90, and 360-count bottles because they were sold without FDA approval for safety and efficacy. This means the product may not be safe for use as intended. Read more at govinfonow.com/recall/42145-jeffreys-drug-store-recalls-domperidone-capsules-10mg-due-to-unapproved.

Source Summary by GovInfoNow · govinfonow.com/recall/42145-jeffreys-drug-store-recalls-domperidone-capsules-10mg-due-to-unapproved · Updated October 8, 2026 · FDA enforcement record: FDA #D-0494-2017

Cite this page

“Jeffreys Drug Store Recalls Domperidone Capsules 10mg Due to Unapproved Safety.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/42145-jeffreys-drug-store-recalls-domperidone-capsules-10mg-due-to-unapproved. Based on FDA recall #D-0494-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0494-2017%22&limit=1).

Why it’s dangerous

The product was marketed without an FDA-approved application for safety and efficacy. This means the product's safety and effectiveness for medical use have not been proven by the FDA, which could lead to health risks if used improperly.

Who’s affected

People who purchased these specific domperidone capsules from Jeffreys Drug Store in Canonsburg, PA, between the dates of manufacture and expiration (Lot #071116-103323, Exp. 1/7/2017). Those using the product for medical purposes without FDA approval are at risk.

How to tell if you have this one

Check for the lot number 071116-103323 and expiration date 1/7/2017 on the bottle. The product was dispensed by Jeffreys Drug Store at 1 North Central Ave. in Canonsburg, PA.

  • Brand
    Jeffreys Drug Store
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot number 071116-103323 and expiration date 1/7/2017 on the bottle.

Where it went and when

Where it was distributed

Distributed in Pennsylvania.

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: yesPANew 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: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

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

States: Pennsylvania.

Recall timeline

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

1. Firm started the recall: Nov 23, 201612. FDA classified it Class I: Feb 27, 201723. Published in FDA’s Enforcement Report: Mar 8, 201734. FDA terminated the recall: Oct 29, 2018420162018
  1. Firm started the recall
  2. FDA classified it Class I
  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-0494-2017 (November 23, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0494-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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