ClearanceBrief
Recall Z-3052-2017 ยท PGW Ear, Nose, And Throat Stereotaxic Instrument

Medtronic Navigation, Inc.

Medtronic Curved Suction 70 9733450 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system. The AxiEM system is an electromagnetic (EM) tracking solution for surgical tools. The system measures an induced voltage cr

DateJun 29, 2017
StatusTerminated
ReasonThe instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Root causeDevice Design
ActionMedtronic sent an Urgent Medical Device Recall letter dated June 25, 2017, via overnight mail on June 29, 2017, to all affected customers. Letters to foreign customers are being handled by geography-specific Regulatory Specialists. Customers were instructed examine their inventory for the affected product and immediately quarantine them for return for Medtronic. Customers with affected product were instructed to contact Medtronic Technical Services at 1-800-595-9709 to receive a return material authorization (RMA) and arrange for their return and no charge replacements. Customers were asked
Quantity149 instruments
DistributionWorldwide Distribution - US (nationwide) and Internationally to Canada.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K153555EM ENT Navigated Suctions
Medtronic Navigation, Inc., Apr 7, 2016