US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 23, 2018 (8 years ago)

Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Dissolution Specifications. High dissolution results were obtained during stability testing.

What was recalled

Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By: Actavis 60 Columbia Rd., Bldg. B Morristown, NJ 07960. NDC 63739-284-10

Recalling firm
Mckesson Packaging Services
NDC code
63739-284-10
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0715-2018

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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