Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380040

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 14026704340641, Batch Numbers: 19FT28, 19GT04, 19GT51, 19KT13, 19LT28, 20BG15, 20ET03, KME20H2609, KME20J3088, KME20K2749, KME20L0640, KME20M1726, KME20M2538, KME21A0858, KME21M2918, KME22B2857, KME22C3373, KME22D0876
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 - Magill, REF 100380040

Product Codes/Lot Numbers:

UDI/DI 14026704340641, Batch Numbers: 19FT28, 19GT04, 19GT51, 19KT13, 19LT28, 20BG15, 20ET03, KME20H2609, KME20J3088, KME20K2749, KME20L0640, KME20M1726, KME20M2538, KME21A0858, KME21M2918, KME22B2857, KME22C3373, KME22D0876