Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180065

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 14026704340504, Batch Numbers: 18JG07, 19AG21, 19BG12, 19HT03, 19HT34, 19JT02, 19LT32, 20AT49, KME20M2642, KME21B0078, KME22D1517, KME22H1720, KME22J0807
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 100180065

Product Codes/Lot Numbers:

UDI/DI 14026704340504, Batch Numbers: 18JG07, 19AG21, 19BG12, 19HT03, 19HT34, 19JT02, 19LT32, 20AT49, KME20M2642, KME21B0078, KME22D1517, KME22H1720, KME22J0807