Duren Health Mart Pharmacy Recalls Domperidone Capsules Due to Processing Controls
Duren Health Mart Pharmacy recalls 100-count Domperidone 10mg capsules (Rx only) because of lack of processing controls. No remedy specified in official notice.
Recall notice
Lack of Processing Controls.
Contact the company
What happened, in plain English
Duren Health Mart Pharmacy is recalling 100-count Domper: 10mg capsules that require a prescription. The recall is due to a lack of processing controls, but no specific remedy is provided in the official notice. Read more at govinfonow.com/recall/39316-duren-health-mart-pharmacy-recalls-domperidone-capsules-due-to-processing.
Source Summary by GovInfoNow · govinfonow.com/recall/39316-duren-health-mart-pharmacy-recalls-domperidone-capsules-due-to-processing · Updated October 5, 2026 · FDA enforcement record: FDA #D-0421-2019
Cite this page
“Duren Health Mart Pharmacy Recalls Domperidone Capsules Due to Processing Controls.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39316-duren-health-mart-pharmacy-recalls-domperidone-capsules-due-to-processing. Based on FDA recall #D-0421-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0421-2019%22&limit=1).
Why it’s dangerous
The recall states there is a lack of processing controls, which could lead to potential quality issues with the medication. However, the specific hazard mechanism is not clearly described in the official notice.
Who’s affected
People who purchased or have the 100-count Domperidone 10mg capsules from Duren Health Mart Pharmacy in Waynesboro, TN. Those with a prescription for this medication are most at risk.
How to tell if you have this one
Check for 100-count Domperidone 10mg capsules with the NDC code 00507-2011-00. These were sold by Duren Health Mart Pharmacy at 215 Dexter Woods Blvd in Waynesboro, TN.
- Brand
Duren Health Mart Pharmacy- Category
Drug
All 6 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 II- Status
Terminated- Distribution
TN only
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0416-2019 | Omeprazole 4 mg/mL Suspension, 150cc to 300 cc per prescription, Rx only, Duren's Health Mart Pharmacy 215 Dexter Woods Blvd. Waynesboro, TN 38485, NDC 00000-0001-07; N/A | 2700 cc |
| D-0417-2019 | Progesterone 10% cream, 12gm to 30gm per prescription, Rx only, Duren's Health Mart Pharmacy 215 Dexter Woods Blvd. Waynesboro, TN 38485, NDC 00000-0002-99; N/A | 200 grams |
| D-0418-2019 | Testosterone 0.1% cream, 30 grams, Rx only, Duren's Health Mart Pharmacy 215 Dexter Woods Blvd. Waynesboro, TN38485, NDC 00000-0000-98; N/A | 300 grams |
| D-0419-2019 | Promethazine Gel 50 mg/mL, 1cc to 10cc per prescription, Rx only, Duren's Health Mart Pharmacy 215 Dexter Woods Blvd. Waynesboro, TN38485, NDC 00002-1901-03; N/A | 876 cc |
| D-0420-2019 | Progesterone 100 mg SR capsules, 30-180 capsules per prescription, Rx only, Duren's Health Mart Pharmacy 215 Dexter Woods Blvd. Waynesboro, TN38485, NDC 00311-2003-01; N/A | 1306 capsules |
| D-0421-2019 | Domperidone 10 mg capsules, 100-count per prescription, Rx only, Duren's Health Mart Pharmacy 215 Dexter Woods Blvd. Waynesboro, TN 38485, NDC 00507-2011-00; N/A | 840 capsules |
What to do — step by step
Check Product Details
Look for the NDC code 00507-2011-00 on the packaging to confirm if you have the recalled product.
Where it went and when
Where it was distributed
Distributed in Tennessee.
FDA distribution: “TN only” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Tennessee.
Recall timeline
FDA terminated this recall 3.1 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- 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-0421-2019 (December 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0421-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.