Class II · Moderate risk Terminated
Domperidone 10 mg capsules
Reason Lack of Processing Controls.
Domperidone capsules 10 mg
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Marketed without an approved NDA/ANDA for which safety and efficacy has not been established.
What was recalled
Domperidone capsules 10 mg, compounded, dispensed in 60, 90, and 360 count bottles, Jeffreys Drug Store 1 North Central Ave. Canonsburg, PA
- Recalling firm
- Jeffreys Drug Store
- Origin
- PA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0494-2017
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.
Other Domperidone recalls
See all
Class II · Moderate risk Terminated
Domperidone BP
Reason Penicillin Cross Contamination: Potential for products to be cross-contaminated with penicillin.
Class II · Moderate risk Terminated
Domperidone active pharmaceutical ingredient packaged in varying…
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they were repackaged in a facility with penicillin products without adequate separation which could introduce the potential for cross contamination with penicillin.
Get an alert if your medication is recalled
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.