Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080075

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 Batch Numbers: 18FT26, 18GG17, 18GG19, 18HG15, 18HG37, 18IG04, 18IG29, 18JG17, 18KG10, 19AT23, 19CT64, 19ET12, 19ET24, 19GT31, 19HT69, 19IT11, 20AT22, 20BT13, 20BT42, 20CT02, 20CT54, 20DT09, 20FT21, 20FT60, 20GT18, KME20H0334, KME21F1534, KME22A2269, KME22B0741, KME22B0896, KME22B1031, KME22C0096, KME22E2348, KME22F2118,
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 112080075

Product Codes/Lot Numbers:

UDI/DI Batch Numbers: 18FT26, 18GG17, 18GG19, 18HG15, 18HG37, 18IG04, 18IG29, 18JG17, 18KG10, 19AT23, 19CT64, 19ET12, 19ET24, 19GT31, 19HT69, 19IT11, 20AT22, 20BT13, 20BT42, 20CT02, 20CT54, 20DT09, 20FT21, 20FT60, 20GT18, KME20H0334, KME21F1534, KME22A2269, KME22B0741, KME22B0896, KME22B1031, KME22C0096, KME22E2348, KME22F2118,