Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060

Class I - Dangerous

🏥 Medical Devices Recalled: May 25, 2023 TELEFLEX Other Medical Devices Nationwide

What Should You Do?

Check if you have this product:
UDI/DI 14026704341266, Batch Numbers: 18GG26, 18GT08, 18GT11, 18IG22, 18IT18, 18JG33, 19AG39, 19ET31, 19GT25, 19IT20, 19KT14, 19KT47, 20AT58, 20CT13, 20FT66, KME20J1463, KME21K0521, KME22A2893, KME22B2215, KME22C2044, KME22G2998, KME22J0859
Do not eat it: Even if it looks and smells fine, do not consume this product.
Throw it away or return it: You can return the product to the store for a full refund.
Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:: TELEFLEX LLC
Reason for Recall:: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: ongoing

Product Information

Full Description:

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060

Product Codes/Lot Numbers:

UDI/DI 14026704341266, Batch Numbers: 18GG26, 18GT08, 18GT11, 18IG22, 18IT18, 18JG33, 19AG39, 19ET31, 19GT25, 19IT20, 19KT14, 19KT47, 20AT58, 20CT13, 20FT66, KME20J1463, KME21K0521, KME22A2893, KME22B2215, KME22C2044, KME22G2998, KME22J0859