Medical device recalls
38685 federal recalls on file. Federal recalls for medical devices — surgical equipment, monitors, diagnostic tools, implants, home health devices. Sourced from the FDA.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080065
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080050
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781070
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781065
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781060
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781055
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781035
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780090
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780085
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780080
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780070
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780065
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780060
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780055
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780050
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IPreformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382040
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380065
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380060
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-07-05FDA-DeviceTELEFLEX LLCClass IEndotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380055
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
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