🔍 RecallPedia

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082100

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 14026704341488, Batch Numbers: 18GG13, 18JG24, 18JG36, 18JT06, 18KG10, 18LG06, 19AG36, 19CG02, 19GT16, 19GT59, 19IT33, 19JT56, 19KT14, 19KT49, 20AT01, 20AT22, 20BG18, 20DT18, 20DT19, 20ET17, KME20H2141, KME20K1809, KME20K2553, KME20L0335, KME20M1341, KME20M2113, KME21A2342, KME21A2668, KME21C0017, KME21F2252, KME21F2345, KME22B1777, KME22B1881, KME22C0019, KME22C0063, KME22C0327, KME22E2679, KME22F0401, KME22H0209, KME22H2251, KME22J2931, KME22J3329, KME22L0218, KME22L0219, KME22L2730, KME22L2731, KME23A2196, KME23A2539, KME23A3169
  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:

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082100

Product Codes/Lot Numbers:

UDI/DI 14026704341488, Batch Numbers: 18GG13, 18JG24, 18JG36, 18JT06, 18KG10, 18LG06, 19AG36, 19CG02, 19GT16, 19GT59, 19IT33, 19JT56, 19KT14, 19KT49, 20AT01, 20AT22, 20BG18, 20DT18, 20DT19, 20ET17, KME20H2141, KME20K1809, KME20K2553, KME20L0335, KME20M1341, KME20M2113, KME21A2342, KME21A2668, KME21C0017, KME21F2252, KME21F2345, KME22B1777, KME22B1881, KME22C0019, KME22C0063, KME22C0327, KME22E2679, KME22F0401, KME22H0209, KME22H2251, KME22J2931, KME22J3329, KME22L0218, KME22L0219, KME22L2730, KME22L2731, KME23A2196, KME23A2539, KME23A3169

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1894-2023

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