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O-Two Medical Technologies Recalls
6 recalls on record · July 19, 2017 to April 10, 2019 · Medical Devices
Recalls by year
17
18
19
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 10, 2019Medical DevicesFDA
O-Two Medical Technologies, Inc. recalls e700 Automatic Transport Ventilator, Model Number 01EVE700
Hazard: There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.
April 10, 2019Medical DevicesFDA
O-Two Medical Technologies, Inc. recalls e600 Automatic Transport Ventilator, Model Number 01EVE600
Hazard: There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.
April 10, 2019Medical DevicesFDA
O-Two Medical Technologies, Inc. recalls e500 Automatic Transport Ventilator, Model Number 01EVE500
Hazard: There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.
August 29, 2018Medical DevicesFDA
O-Two Medical Technologies, Inc. recalls O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000
Hazard: Higher levels of nitrous oxide delivered than specification
July 19, 2017Medical DevicesFDA
O-Two Medical Technologies, Inc. recalls Burn Relief¿, MODEL #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200, CATALOG #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200 -
Hazard: For lack of evidence to validate effectiveness of sterilization dose, O-Two Medical Technologies Inc. hereby announces a voluntary medical device recall of the suspected batches of Burn Relief¿ products to prevent potential contamination. .
July 19, 2017Medical DevicesFDA
O-Two Medical Technologies, Inc. recalls O-Two Adult Ventilation Timer, MODEL #(s): 01BM1000-CS, 01BM3201-MOTP-CS, 01BM3201-MOTL-CS, CATALOG #(s): 01BM1000 ---
Hazard: Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the malfunctioning device was reported to be twice that of the rate noted on the label.