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RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480030

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 14026704341501, Batch Numbers: 18GG16, 18HG10, 18HG25, 18IG03, 19BG12, 19BG16, 19CT42, 19CT64, 19DT36, 19ET09, 19ET31, 19ET53, 19GT02, 19IT38, 19JT21, 19JT55, 19KT20, 19KT37, 19LT31, 20AT40, 20DT01, 20DT20, 20ET30, 20GT38, KME20J3096, KME20K2145, KME20L1345, KME20M1802, KME21B0621, KME21B2379, KME21C0168, KME22A1495, KME22A2394, KME22A2396, KME22B2938, KME22C2668, KME22C2669, KME22C2687, KME22D3223, KME22E1149, KME22E2287, KME22G1233, KME22G1879, KME23B0133, KME23B0560, KME23B0717, KME23B2197
  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:

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480030

Product Codes/Lot Numbers:

UDI/DI 14026704341501, Batch Numbers: 18GG16, 18HG10, 18HG25, 18IG03, 19BG12, 19BG16, 19CT42, 19CT64, 19DT36, 19ET09, 19ET31, 19ET53, 19GT02, 19IT38, 19JT21, 19JT55, 19KT20, 19KT37, 19LT31, 20AT40, 20DT01, 20DT20, 20ET30, 20GT38, KME20J3096, KME20K2145, KME20L1345, KME20M1802, KME21B0621, KME21B2379, KME21C0168, KME22A1495, KME22A2394, KME22A2396, KME22B2938, KME22C2668, KME22C2669, KME22C2687, KME22D3223, KME22E1149, KME22E2287, KME22G1233, KME22G1879, KME23B0133, KME23B0560, KME23B0717, KME23B2197

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1896-2023

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