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Vascular Technology Recalls
5 recalls on record · July 16, 2014 to September 19, 2018 · Medical Devices
Recalls by year
14
18
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 19, 2018Medical DevicesFDA
Vascular Technology, Inc. recalls VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref. Number: 108910 Intraoperative (microvascular and
Hazard: Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver
July 16, 2014Medical DevicesFDA
Vascular Technology, Inc. recalls VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative
Hazard: Report of the product penetrating the sterile barrier; this could render the product unsterile.
July 16, 2014Medical DevicesFDA
Vascular Technology, Inc. recalls 07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe is intended for the intraoperative and
Hazard: Report of the product penetrating the sterile barrier; this could render the product unsterile.
July 16, 2014Medical DevicesFDA
Vascular Technology, Inc. recalls 07-150-10 MIZUHO, DOPPLER PROBE, SLIM, BX 4, REF 138660 The Doppler probe is intended for the intraoperative and tran
Hazard: Report of the product penetrating the sterile barrier; this could render the product unsterile.
July 16, 2014Medical DevicesFDA
Vascular Technology, Inc. recalls 07-150-07 MIZUHO, MAL DISP DOPPLER PROBE BX 4, REF 138200 The Doppler probe is intended for the intraoperative and tr
Hazard: Report of the product penetrating the sterile barrier; this could render the product unsterile.