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TELEFLEX Recalls

151 recalls on record · February 18, 2015 to July 8, 2026 · Medical Devices

Recalls by year

15
22
23
26

Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082085
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082075
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082065
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082060
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082055
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080100
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080055
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781075
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781045
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781040
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382030
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181050
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181045
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181040
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180070
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180065
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180060
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180055
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180050
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180045
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.