🔍 RecallPedia

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095

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 14026704341471, Batch Numbers: 18HG08, 18HT04, 18IG29, 18IT04, 18JT16, 18KG37, 18KT27, 18LT16, 19BG02, 19CG02, 19CT04, 19CT72, 19GT25, 19HT19, 19HT47, 19JT05, 19KT55, 19LT08, 20AT13, 20CT02, 20CT29, 20DT32, 20GT23, 20GT44, KME20H1486, KME20J1899, KME20K2166, KME20L1592, KME20L2462, KME20L2557, KME20M2115, KME20M2198, KME21A2346, KME21E1393, KME21K1818, KME22B1259, KME22B1420, KME22B1854, KME22C0677, KME22C0713, KME22C0844, KME22C1612, KME22C2606, KME22C2757, KME22D1593, KME22D1778, KME22E1285, KME22E2362, KME22F1401, KME22F2452, KME23A0557, KME23A0763
  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 112082095

Product Codes/Lot Numbers:

UDI/DI 14026704341471, Batch Numbers: 18HG08, 18HT04, 18IG29, 18IT04, 18JT16, 18KG37, 18KT27, 18LT16, 19BG02, 19CG02, 19CT04, 19CT72, 19GT25, 19HT19, 19HT47, 19JT05, 19KT55, 19LT08, 20AT13, 20CT02, 20CT29, 20DT32, 20GT23, 20GT44, KME20H1486, KME20J1899, KME20K2166, KME20L1592, KME20L2462, KME20L2557, KME20M2115, KME20M2198, KME21A2346, KME21E1393, KME21K1818, KME22B1259, KME22B1420, KME22B1854, KME22C0677, KME22C0713, KME22C0844, KME22C1612, KME22C2606, KME22C2757, KME22D1593, KME22D1778, KME22E1285, KME22E2362, KME22F1401, KME22F2452, KME23A0557, KME23A0763

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1893-2023

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