US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 11, 2018 (8 years ago)

Monsel's Solution (Ferric Subsulfate), 20%, packaged as 12 single application vials and…

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

Why it was recalled

CGMP Deviations: Products not manufactured under current good manufacturing practices.

What was recalled

Monsel's Solution (Ferric Subsulfate), 20%, packaged as 12 single application vials and 12 applicators, 8 mL per box, Manufactured For: MedGyn Products, Inc., 100 W. Industrial Rd., Addison, IL 60101 USA; Manufactured By: BioDiagnostics Intl, 555 West Lambert Road Unit-C, Brea, CA 92821, NDC 42721-112-08.

Recalling firm
BioDiagnostic International
NDC code
42721-112-08
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0874-2018

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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