Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170055

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 4026704319541, Batch numbers: 18FG18, 18GG14, 18GG31, 18HG22, 18KG23, 19BG12, 19ET72, 19IT25, 20AT25, 20AT32, 20BT05, 20BT37, 20BT47, 20ET21, KME20G0383, KME20K0936, KME20K2587, KME20L1469, KME20L2378, KME21G0756, KME21M0313, KME21M1832, KME22B0193, KME22D1787, KME22F1665
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:

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170055

Product Codes/Lot Numbers:

UDI/DI 4026704319541, Batch numbers: 18FG18, 18GG14, 18GG31, 18HG22, 18KG23, 19BG12, 19ET72, 19IT25, 20AT25, 20AT32, 20BT05, 20BT37, 20BT47, 20ET21, KME20G0383, KME20K0936, KME20K2587, KME20L1469, KME20L2378, KME21G0756, KME21M0313, KME21M1832, KME22B0193, KME22D1787, KME22F1665