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microTargeting™ Electrode and Insertion Tube Kit

FHC, INC. · Model FC7100-00132 · UDI-DI 10873263001322

GZLHAW Prescription
2
510(k) clearances
228
Adverse events (3 deaths)
24
Recalls
24
Facilities

Description

Array Insertion Electrode/Tube with Stylet Kit, 5x, Sterile, for use with Nexframe and microTargeting Drive. Contains: IT(AR8): Insertion Tube w/ Stylet. MTDPBN(PA)(DB2): microTargeting Electrode. Individual Specifications: IT(AR8) - 217mm tube length, 0.89mm OD, 0.58mm ID MTDPBN(PA)(DB2) - 249.2mm electrode length, 10mm differential length, 234.2mm protective tube length. 1 Meg RZAP, 0.56mm od

Recalls

DateFirmReason
2024-09-19Ad-Tech Medical Instrument CorporationAd-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style contact SD electrodes where the MR Conditional symbol was incorrectly p
2024-09-19Ad-Tech Medical Instrument CorporationAd-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style contact SD electrodes where the MR Conditional symbol was incorrectly p
2024-09-19Ad-Tech Medical Instrument CorporationAd-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style contact SD electrodes where the MR Conditional symbol was incorrectly p
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.