Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060

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 14026704340856, Batch Numbers: 18FG02, 18FG28, 18FT08, 18FT33, 18JG15, 18KG23, 18KG39, 20BT17, 20CT07, KME20H1758, KME20H2730, KME21D0828, KME21J0120, KME21J1583, KME22A2339, KME22B0949, KME22B1778, KME22C2310, KME22D1804, KME22F0417, KME22F0556, KME22F1739
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 uncuffed/plain - Murphy, REF 100382060

Product Codes/Lot Numbers:

UDI/DI 14026704340856, Batch Numbers: 18FG02, 18FG28, 18FT08, 18FT33, 18JG15, 18KG23, 18KG39, 20BT17, 20CT07, KME20H1758, KME20H2730, KME21D0828, KME21J0120, KME21J1583, KME22A2339, KME22B0949, KME22B1778, KME22C2310, KME22D1804, KME22F0417, KME22F0556, KME22F1739