Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055

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 14026704340849, Batch Numbers: 18FG21, 18FG33, 18FT17, 18FT31, 18GT06, 18HG06, 18HG15, 18IT06, 18JG14, 18JT12, 18KG10, 19AG05, 19AT23, 19BG10, 19BG21, 19BG26, 19BT08, 20CT47, 20DT01, 20GG45, 20GT40, KME20H0294, KME20H3036, KME20J0600, KME20J2166, KME20K1116, KME20K1206, KME20K3277, KME20L1040, KME20L1224, KME22F2548
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 100382055

Product Codes/Lot Numbers:

UDI/DI 14026704340849, Batch Numbers: 18FG21, 18FG33, 18FT17, 18FT31, 18GT06, 18HG06, 18HG15, 18IT06, 18JG14, 18JT12, 18KG10, 19AG05, 19AT23, 19BG10, 19BG21, 19BG26, 19BT08, 20CT47, 20DT01, 20GG45, 20GT40, KME20H0294, KME20H3036, KME20J0600, KME20J2166, KME20K1116, KME20K1206, KME20K3277, KME20L1040, KME20L1224, KME22F2548