ClearanceBrief
Recall Z-1374-2023 ยท FHW Device, Impotence, Mechanical/Hydraulic

Coloplast Manufacturing US, LLC

Titan 0-Deg Scrotal 20 Cm, Catalog Number ES89202400; inflatable penile Prosthesis

DateApr 12, 2023 (initiated Mar 1, 2023)
StatusOpen, Classified
ReasonXXX
Root causeProcess change control
ActionThe firm issued an URGENT MEDICAL DEVICE VOLUNTARY RECALL notice on 03/01/2023 by UPS next day air. The notice explained the issue and the hazard to health. The notice requests the removal and return of the affected product. Distributors are instructed to notify their customers. For further questions, please contact the Coloplast Customer Service team directly at (800) 258-3476, or by email urology@coloplast.com.
Quantity20 units
DistributionWorldwide distribution - US Nationwide and the countries of Turkey, Italy, Germany, Belgium, France, United Kingdom, Spain, Portugal.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.