June 2018 FDA Recall Drug by Biodiagnostic International
D-0874-2018 - CGMP Deviations

This Class II drug recall was voluntarily initiated by Biodiagnostic International on June 11, 2018 for the product Drug. The FDA reported the reason for recall as cgmp deviations. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0874-2018

Reason for Recall
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Initiated
06-11-2018
Reported
06-20-2018
Quantity
1000 boxes

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
BioDiagnostic International
Product was distributed to one sole customer in Illinois who further distributed Nationwide in the USA.
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.

Batch or Lot Expiration Information

Lot# All lots within expiry