US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Dec 28, 2023 (3 years ago)

Quality Choice No Drip Severe Congestion Nasal Pump Mist, Oxymetazoline hydrochloride…

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

Why it was recalled

CGMP Deviations: Firm reported possible microbial contamination in the purified water used in the manufacturing of the products. No contamination was found in the final products.

What was recalled

Quality Choice No Drip Severe Congestion Nasal Pump Mist, Oxymetazoline hydrochloride 0.05%, Nasal Decongestant, 12 Hours, 1 fl. oz. bottle, Distributed by C.D.M.A., Inc., 43157 W 9 Mile Rd., Novi, MI 48375, NDC 63868-608-01, UPC 6-35515-98846-0

Recalling firm
Seaway Pharma Inc.
NDC code
63868-608-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0217-2024

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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