ClearanceBrief
Recall Z-3000-2011 ยท JAQ System, Applicator, Radionuclide, Remote-Controlled

Varian Medical Systems, Inc. Oncology Systems

Titanium Fletcher-style Applicator Set - Defined Geometry - CT Compatible with Titanium intrauterine probe with stopper length 70 mm, 30 degree angle. Varian Medical Systems, Palo Alto, CA; Manufactured by Varian Medical Systems Haan GmbH, Haan, Germany. To treat cancer of the uterus, cervix, endometrium and vagina.

DateAug 11, 2011 (initiated Jul 13, 2011)
StatusTerminated
ReasonPotential of weld failure of the Titanium intrauterine probe at the cervical stopper.
Root causeDevice Design
ActionVarian Medical Systems sent an "URGENT MEDICAL DEVICE CORRECTION/URGENT FIELD SAFETY NOTICE" letter dated July 13, 2011 to all affected customers. The letter describes the product, problem, and the actions to be taken by the customers. The letter instructs customers to return all affected product to Varian Brachy Therapy by using the contact information provided in the letter. Replacement product will be provided free of charge to the customers. Customers should contact their local Varian Customer Support District or Regional Manager for questions regarding this notice.
Quantity437 - all sizes
DistributionWorldwide Distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K983436GAMMAMED PLUS HIGH DOSE RATE REMOTE AFTERLOADING SYSTEM
Gammamed USA, Oct 29, 1998