Class II · Moderate risk
Domperidone 10 mg capsules
Lack of Processing Controls.
Is Domperidone recalled?
Not under an active recall.
Domperidone was recalled 4 times in the past — all now closed. Most recent: Dec 17, 2018.
Most common reason: Cross-contamination (2 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Domperidone. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Domperidone recalls on record
none so far in 2026; 4 on record, newest first
Class I · High risk
Domperidone capsules 10 mg
Marketed without an approved NDA/ANDA for which safety and efficacy has not been established.
Class II · Moderate risk
Domperidone BP
Penicillin Cross Contamination: Potential for products to be cross-contaminated with penicillin.
Class II · Moderate risk
Domperidone active pharmaceutical ingredient packaged in varying…
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.
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