🔍 RecallPedia

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780050

Class I - Dangerous
🏥 Medical Devices Recalled: May 25, 2023 TELEFLEX Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704341068, Batch Numbers: 18FG12, 18FG24, 18GG03, 18GT26, 18HG24, 18IG24, 18JG07, 18KG34, 18LG11, 18LG31, 19AG09, 19AG11, 19AG21, 19AG36, 19CG07, 19CT36, 19DT06, 19FT18, 19GT44, 19JT01, 19KT37, 19LT04, 19LT32, 20AT09, 20BT53, 20CT24, 20DT24, 20ET50, 20ET56, 20FT36, 20FT58, KME20J1117, KME20M0952, KME21A0202, KME21A2486, KME21B0747, KME21C0326, KME22A1676, KME22B0553, KME22B1725, KME22C2818, KME22D0293, KME22D2681, KME22F0733, KME22G0349, KME22G3043, KME22H1792, KME22J2836, KME22K0470, KME22K0876, KME22M1319, KME22M1954, KME23A0157, KME23A1282, KME23A1422, KME23A1483, KME23A2002, KME23A2278, KME23B0506
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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 Murphy Eye, High Volume, Low Pressure Cuff, REF 111780050

Product Codes/Lot Numbers:

UDI/DI 14026704341068, Batch Numbers: 18FG12, 18FG24, 18GG03, 18GT26, 18HG24, 18IG24, 18JG07, 18KG34, 18LG11, 18LG31, 19AG09, 19AG11, 19AG21, 19AG36, 19CG07, 19CT36, 19DT06, 19FT18, 19GT44, 19JT01, 19KT37, 19LT04, 19LT32, 20AT09, 20BT53, 20CT24, 20DT24, 20ET50, 20ET56, 20FT36, 20FT58, KME20J1117, KME20M0952, KME21A0202, KME21A2486, KME21B0747, KME21C0326, KME22A1676, KME22B0553, KME22B1725, KME22C2818, KME22D0293, KME22D2681, KME22F0733, KME22G0349, KME22G3043, KME22H1792, KME22J2836, KME22K0470, KME22K0876, KME22M1319, KME22M1954, KME23A0157, KME23A1282, KME23A1422, KME23A1483, KME23A2002, KME23A2278, KME23B0506

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1943-2023

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