US Drug Recall Register
Class III · Low risk Terminated Initiated Jun 7, 2016 (10 years ago)

Cyproheptadine Hydrochloride Syrup, Oral Solution USP, 2 mg/5 mL, packaged in an amber…

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

Why it was recalled

Subpotency: product assayed and found OOS for cyproheptadine

What was recalled

Cyproheptadine Hydrochloride Syrup, Oral Solution USP, 2 mg/5 mL, packaged in an amber glass 473 mL (one pint) bottle with child-resistant screw closure, Rx only, Distributed by: Rising Pharmaceuticals, Inc., Allendale, NJ 07401, Manufactured by: Lyne Laboratories, Inc., Brockton, MA 02301, NDC 64980-0504-48

Recalling firm
Lyne Laboratories, Inc.
NDC code
64980-0504-48
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1062-2016

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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