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RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040

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 14026704341525, Batch Numbers: 18FG14, 18FG22, 18JG08, 18KG25, 18LG04, 18LG30, 19DT35, 19DT36, 19ET09, 19ET31, 19ET51, 19HT60, 19IT32, 19IT43, 20AT06, 20AT39, 20BT01, 20BT53, 20CT12, 20CT27, 20CT54, 20DT04, 20ET30, 20FT58, KME20G0182, KME20H0372, KME20H0373, KME20J0924, KME20J2043, KME21C2368, KME21K1187, KME21K1188, KME21K1977, KME21M1084, KME21M1842, KME21M1845, KME21M2733, KME21M2734, KME21M2735, KME21M2736, KME22B2019, KME22C1693, KME22D0057, KME22D0180, KME22D0819, KME22D1066, KME22D3269, KME22E0602, KME22E2648, KME22E2681, KME22F1440, KME22F1692, KME22F2455, KME22G2312, KME22H1126, KME22H1212, KME22H2302, KME22J1615, KME22K0283, KME22K0632, KME22K1096, KME22M1155, KME22M1478, KME22M1659, KME23B3174
  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 112480040

Product Codes/Lot Numbers:

UDI/DI 14026704341525, Batch Numbers: 18FG14, 18FG22, 18JG08, 18KG25, 18LG04, 18LG30, 19DT35, 19DT36, 19ET09, 19ET31, 19ET51, 19HT60, 19IT32, 19IT43, 20AT06, 20AT39, 20BT01, 20BT53, 20CT12, 20CT27, 20CT54, 20DT04, 20ET30, 20FT58, KME20G0182, KME20H0372, KME20H0373, KME20J0924, KME20J2043, KME21C2368, KME21K1187, KME21K1188, KME21K1977, KME21M1084, KME21M1842, KME21M1845, KME21M2733, KME21M2734, KME21M2735, KME21M2736, KME22B2019, KME22C1693, KME22D0057, KME22D0180, KME22D0819, KME22D1066, KME22D3269, KME22E0602, KME22E2648, KME22E2681, KME22F1440, KME22F1692, KME22F2455, KME22G2312, KME22H1126, KME22H1212, KME22H2302, KME22J1615, KME22K0283, KME22K0632, KME22K1096, KME22M1155, KME22M1478, KME22M1659, KME23B3174

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1898-2023

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