Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704340832, Batch Numbers: 18FG02, 18FT26, 18FT35, 18GG26, 18HT18, 18IG04, 18IG10, 18JG36, 18JT06, 18JT10, 18KG23, 18KT30, 18LG06, 18LT18, 19BG16, 19BG21, 19CG06, 19DT16, 19DT39, 19GT58, 19IT20, 19JT46, 19KT29, 19LT46, 20AT26, 20CT11, 20CT38, 20DT13, 20DT23, 20GG45, 20GT24, 20GT41, 20GT44, KME20H0293, KME20H1490, KME20H2049, KME20L1755, KME20L2383, KME20L2596, KME20M2056, KME21M2476, KME22A1524, KME22D0857, KME22D2479, KME22D3022, KME22F2427, KME22G0200, KME22G1191
  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 100382050

Product Codes/Lot Numbers:

UDI/DI 14026704340832, Batch Numbers: 18FG02, 18FT26, 18FT35, 18GG26, 18HT18, 18IG04, 18IG10, 18JG36, 18JT06, 18JT10, 18KG23, 18KT30, 18LG06, 18LT18, 19BG16, 19BG21, 19CG06, 19DT16, 19DT39, 19GT58, 19IT20, 19JT46, 19KT29, 19LT46, 20AT26, 20CT11, 20CT38, 20DT13, 20DT23, 20GG45, 20GT24, 20GT41, 20GT44, KME20H0293, KME20H1490, KME20H2049, KME20L1755, KME20L2383, KME20L2596, KME20M2056, KME21M2476, KME22A1524, KME22D0857, KME22D2479, KME22D3022, KME22F2427, KME22G0200, KME22G1191

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1876-2023

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