US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jul 23, 2026 (41 days ago)

Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only, Distributed by…

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

Why it was recalled

shortfill; reports of empty capsules.

What was recalled

Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India, NDC 59651-719-99

Recalling firm
Aurobindo Pharma USA Inc
NDC code
59651-719-99
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0733-2026

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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