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 8, 2026Medical DevicesFDA
TELEFLEX LLC recalls Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips
Hazard: Due to out-of-specification, or potential out-of-specification, levels of endotoxins
July 12, 2023Medical DevicesFDA
TELEFLEX LLC recalls Pilling LOWSLEY PROSTATIC TRACTOR STR, REF 243201; retractor
Hazard: There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
July 12, 2023Medical DevicesFDA
TELEFLEX LLC recalls Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor
Hazard: There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
July 12, 2023Medical DevicesFDA
TELEFLEX LLC recalls Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Hazard: There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080090
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 112080085
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 112080080
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 112080075
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 112080070
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 112080065
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 112080060
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 112080050
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 111781080
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 111781070
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 111781065
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 111781060
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 111781055
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 111781050
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 111781035
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 111780090
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 111780085
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 111780080
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 111780070
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 111780065
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 111780060
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 111780055
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 111780050
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 111780045
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 111780040
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 111780035
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.