Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035

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 14026704340443, Batch Numbers: 18IG24, 18JG07, 18LG06, 18LG33, 19AG36, 19CT69, 19DT42, 19ET34, 19FT19, 19FT29, 19HT34, 19IT43, 19JT02, 19LT08, 19LT32, 20ET56, KME20K1811, KME20M0947, KME21A0060, KME21A2390, KME21B0599, KME22D1515, KME22G0175, KME22K0607, KME22K3167, KME23A1884
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:

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035

Product Codes/Lot Numbers:

UDI/DI 14026704340443, Batch Numbers: 18IG24, 18JG07, 18LG06, 18LG33, 19AG36, 19CT69, 19DT42, 19ET34, 19FT19, 19FT29, 19HT34, 19IT43, 19JT02, 19LT08, 19LT32, 20ET56, KME20K1811, KME20M0947, KME21A0060, KME21A2390, KME21B0599, KME22D1515, KME22G0175, KME22K0607, KME22K3167, KME23A1884