🔍 RecallPedia

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025

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 14026704340788, Batch Numbers: 18FG22, 18FG31, 18FT13, 18GG16, 18GG34, 18GT12, 18HG08, 18IG13, 18IG14, 18JG09, 18JG14, 18JG35, 18KG08, 18LG15, 19AG04, 19AG07, 19AG21, 19BG12, 19CT37, 19CT41, 19CT44, 19CT64, 19ET57, 19FT25, 19GT04, 19GT29, 19KT65, 19LT03, 19LT27, 20AT37, 20BT15, 20CT12, 20DT04, 20ET03, 20ET33, 20FT21, 20FT40, 20GG41, KME20K2027, KME20K3208, KME21C1802, KME21C2684, KME21D0352, KME21D0601, KME21D1281, KME21D1818, KME21E1427, KME21M3077, KME22B1025, KME22B1089, KME22C0099, KME22E0297, KME22F0538, KME22F2559, KME22F2561, KME22G0176, KME22H1542, KME22K0062, KME22K0425, KME22K2437, KME22K2588, KME22L2985
  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 100382025

Product Codes/Lot Numbers:

UDI/DI 14026704340788, Batch Numbers: 18FG22, 18FG31, 18FT13, 18GG16, 18GG34, 18GT12, 18HG08, 18IG13, 18IG14, 18JG09, 18JG14, 18JG35, 18KG08, 18LG15, 19AG04, 19AG07, 19AG21, 19BG12, 19CT37, 19CT41, 19CT44, 19CT64, 19ET57, 19FT25, 19GT04, 19GT29, 19KT65, 19LT03, 19LT27, 20AT37, 20BT15, 20CT12, 20DT04, 20ET03, 20ET33, 20FT21, 20FT40, 20GG41, KME20K2027, KME20K3208, KME21C1802, KME21C2684, KME21D0352, KME21D0601, KME21D1281, KME21D1818, KME21E1427, KME21M3077, KME22B1025, KME22B1089, KME22C0099, KME22E0297, KME22F0538, KME22F2559, KME22F2561, KME22G0176, KME22H1542, KME22K0062, KME22K0425, KME22K2437, KME22K2588, KME22L2985

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1934-2023

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