Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080080

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: 18FG02, 18GG15, 18IG13, 18IG22, 18JG17, 18JG38, 19BG21, 19DT19, 19GT24, 19HT26, 19JT20, 19KT19, 19KT38, 19KT50, 19LT46, 19LT47, 20AT06, 20BT09, 20DT23, 20GG39, KME21G0866, KME22A2268, KME22B0062
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 112080080

Product Codes/Lot Numbers:

UDI/DI 14026704341266, Batch Numbers: 18FG02, 18GG15, 18IG13, 18IG22, 18JG17, 18JG38, 19BG21, 19DT19, 19GT24, 19HT26, 19JT20, 19KT19, 19KT38, 19KT50, 19LT46, 19LT47, 20AT06, 20BT09, 20DT23, 20GG39, KME21G0866, KME22A2268, KME22B0062