🔍 RecallPedia

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382040

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 14026704340818, Batch Numbers: 18FG31, 18FG33, 18FT13, 18GG15, 18HG08, 18HG10, 18HG25, 18IG13, 18JG08, 18KG09, 18KG33, 18LG01, 19BG12, 19BG35, 19ET09, 19FT12, 19GT05, 19IT11, 19KT20, 19KT38, 20AT37, 20CT12, 20CT53, 20DT04, 20ET56, 20FT21, 20FT43, 20GT18, KME20G0126, KME20H0286, KME20H1091, KME20H2041, KME20J2613, KME20K0326, KME20K0601, KME20M0209, KME20M1518, KME21B1133, KME21B1830, KME21C1573, KME21C1675, KME21C2245, KME21C3124, KME21D0525, KME21J0629, KME21K0797, KME21L2516, KME21L2526, KME21M0868, KME22C2637, KME22D0032, KME22D0811, KME22D0943, KME22D1009, KME22E0606, KME22E1274, KME22E2288
  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 uncuffed/plain - Murphy, REF 100382040

Product Codes/Lot Numbers:

UDI/DI 14026704340818, Batch Numbers: 18FG31, 18FG33, 18FT13, 18GG15, 18HG08, 18HG10, 18HG25, 18IG13, 18JG08, 18KG09, 18KG33, 18LG01, 19BG12, 19BG35, 19ET09, 19FT12, 19GT05, 19IT11, 19KT20, 19KT38, 20AT37, 20CT12, 20CT53, 20DT04, 20ET56, 20FT21, 20FT43, 20GT18, KME20G0126, KME20H0286, KME20H1091, KME20H2041, KME20J2613, KME20K0326, KME20K0601, KME20M0209, KME20M1518, KME21B1133, KME21B1830, KME21C1573, KME21C1675, KME21C2245, KME21C3124, KME21D0525, KME21J0629, KME21K0797, KME21L2516, KME21L2526, KME21M0868, KME22C2637, KME22D0032, KME22D0811, KME22D0943, KME22D1009, KME22E0606, KME22E1274, KME22E2288

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1935-2023

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