US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 17, 2018 (8 years ago)

Domperidone 10 mg capsules, 100-count per prescription, Rx only, Duren's Health Mart…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Processing Controls.

What was recalled

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

Recalling firm
Duren Health Mart Pharmacy
NDC code
00507-2011-00
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0421-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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