🔍 RecallPedia

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480025

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 14026704341495, Batch Numbers: 18FG31, 18GT32, 18IG03, 18IG29, 18KG08, 18LG03, 19AG08, 19AG38, 19BG12, 19BG35, 19DT13, 19DT36, 19ET51, 19FT12, 19FT28, 19GT02, 19HT05, 19HT79, 19IT59, 19LT08, 19LT31, 20BG15, 20BT01, 20CT07, 20DT24, 20ET53, 20GT38, KME20H2416, KME20H2417, KME20J1068, KME20K2143, KME20K2598, KME20L0449, KME20L1346, KME20M0127, KME20M1797, KME21A0348, KME21B0087, KME21B0465, KME21C0163, KME21C1805, KME21C2447, KME21C2688, KME21C3244, KME21K2877, KME22A1408, KME22A2390, KME22A2545, KME22B0845, KME22B2017, KME22B2848, KME22C2802, KME22E0598, KME22E2130, KME22E2191, KME22G1878, KME22G2593, KME22H0532, KME22H1185, KME22H2178, KME22H2180, KME22J1309, KME22J2321
  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 112480025

Product Codes/Lot Numbers:

UDI/DI 14026704341495, Batch Numbers: 18FG31, 18GT32, 18IG03, 18IG29, 18KG08, 18LG03, 19AG08, 19AG38, 19BG12, 19BG35, 19DT13, 19DT36, 19ET51, 19FT12, 19FT28, 19GT02, 19HT05, 19HT79, 19IT59, 19LT08, 19LT31, 20BG15, 20BT01, 20CT07, 20DT24, 20ET53, 20GT38, KME20H2416, KME20H2417, KME20J1068, KME20K2143, KME20K2598, KME20L0449, KME20L1346, KME20M0127, KME20M1797, KME21A0348, KME21B0087, KME21B0465, KME21C0163, KME21C1805, KME21C2447, KME21C2688, KME21C3244, KME21K2877, KME22A1408, KME22A2390, KME22A2545, KME22B0845, KME22B2017, KME22B2848, KME22C2802, KME22E0598, KME22E2130, KME22E2191, KME22G1878, KME22G2593, KME22H0532, KME22H1185, KME22H2178, KME22H2180, KME22J1309, KME22J2321

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1895-2023

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