RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480035

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704341518, Batch Numbers: 18GG15, 18GG16, 18IG01, 18IG03, 18IG04, 18IG13, 18LG30, 19BG16, 19BG35, 19DT35, 19ET51, 19GT51, 19IT38, 19JT20, 19JT50, 19KT37, 19KT60, 19LT03, 19LT27, 20AT54, 20BT42, 20BT51, 20CT07, 20CT54, 20ET30, 20FT43, KME20H2894, KME20J0754, KME20J3097, KME20M2591, KME20M3049, KME20M3050, KME21A0349, KME21A3147, KME21A3239, KME21B1099, KME21C1766, KME21C2690, KME21C3242, KME21D0295, KME21D2960, KME21K1922, KME21M0820, KME21M2050, KME21M3073, KME22A0416, KME22A1499, KME22B2850, KME22C1453, KME22C1455, KME22C2694, KME22D1761, KME22D2536, KME22E0601, KME22F2453, KME22G0614, KME22G1180, KME22G1181, KME22G1876, KME22H2913, KME22H3442, KME22J2322, KME22J3348, KME22L1190, KME22L1191, KME22L1547, KME23A2353, KME23A2534, KME23B0590, KME23C0083
  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 112480035

Product Codes/Lot Numbers:

UDI/DI 14026704341518, Batch Numbers: 18GG15, 18GG16, 18IG01, 18IG03, 18IG04, 18IG13, 18LG30, 19BG16, 19BG35, 19DT35, 19ET51, 19GT51, 19IT38, 19JT20, 19JT50, 19KT37, 19KT60, 19LT03, 19LT27, 20AT54, 20BT42, 20BT51, 20CT07, 20CT54, 20ET30, 20FT43, KME20H2894, KME20J0754, KME20J3097, KME20M2591, KME20M3049, KME20M3050, KME21A0349, KME21A3147, KME21A3239, KME21B1099, KME21C1766, KME21C2690, KME21C3242, KME21D0295, KME21D2960, KME21K1922, KME21M0820, KME21M2050, KME21M3073, KME22A0416, KME22A1499, KME22B2850, KME22C1453, KME22C1455, KME22C2694, KME22D1761, KME22D2536, KME22E0601, KME22F2453, KME22G0614, KME22G1180, KME22G1181, KME22G1876, KME22H2913, KME22H3442, KME22J2322, KME22J3348, KME22L1190, KME22L1191, KME22L1547, KME23A2353, KME23A2534, KME23B0590, KME23C0083

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1897-2023

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