Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704340801, Batch Numbers: 18GG15, 18GT32, 18IG13, 18KG24, 18KG33, 18KG34, 18LG01, 18LG03, 19CG05, 19CT36, 19CT72, 19DT13, 19KT20, 20AT05, 20AT50, 20BG19, 20BT43, 20DT01, 20DT04, 20DT24, 20ET30, 20FT21, 20FT43, 20FT58, 20FT68, 20GT22, KME20G0092, KME20K0870, KME20L1581, KME20L1894, KME20M3043, KME21B0039, KME21B1553, KME21C0891, KME21C0930, KME21C1580, KME21L2524, KME22B0933, KME22C2632, KME22C2804, KME22D1106, KME22D2022, KME22D2157, KME22D2462, KME22D2650, KME22D3220, KME22D3334, KME22E0292, KME22E0669, KME22E2685, KME22E2686, KME22F1707, KME22F2556, KME22H1215, KME22J2124, KME22K0712, KME22K0713, KME22K1577, KME22K2171, KME22K2382, KME22K2545, KME22L1846, KME22L2147, KME22L2341, KME22L2372, KME22L2411, KME22M1269, KME22M2426
  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 100382035

Product Codes/Lot Numbers:

UDI/DI 14026704340801, Batch Numbers: 18GG15, 18GT32, 18IG13, 18KG24, 18KG33, 18KG34, 18LG01, 18LG03, 19CG05, 19CT36, 19CT72, 19DT13, 19KT20, 20AT05, 20AT50, 20BG19, 20BT43, 20DT01, 20DT04, 20DT24, 20ET30, 20FT21, 20FT43, 20FT58, 20FT68, 20GT22, KME20G0092, KME20K0870, KME20L1581, KME20L1894, KME20M3043, KME21B0039, KME21B1553, KME21C0891, KME21C0930, KME21C1580, KME21L2524, KME22B0933, KME22C2632, KME22C2804, KME22D1106, KME22D2022, KME22D2157, KME22D2462, KME22D2650, KME22D3220, KME22D3334, KME22E0292, KME22E0669, KME22E2685, KME22E2686, KME22F1707, KME22F2556, KME22H1215, KME22J2124, KME22K0712, KME22K0713, KME22K1577, KME22K2171, KME22K2382, KME22K2545, KME22L1846, KME22L2147, KME22L2341, KME22L2372, KME22L2411, KME22M1269, KME22M2426

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1875-2023

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