Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080070
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704341266, Batch Numbers: 18FG19, 18GG19, 18HG28, 18IG06, 18IG19, 18JG13, 18JG17, 18KG13, 18LT07, 19BG19, 19CT26, 19DT20, 19ET12, 19ET36, 19HT26, 19HT69, 19JT21, 19KT14, 19LT31, 19LT51, 20AT22, 20AT58, 20BT13, 20BT42, 20CT13, 20DT10, 20ET12, 20FT11, 20FT19, 20GG40, 20GT38, KME20K2577, KME20L1985, KME20M1771, KME20M1772, KME21F1585, KME21J0644, KME21J1078, KME22A1109, KME22A1781, KME22B0401, KME22F1174, KME22F2171, KME22G1295, KME22G2999
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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 Magill, High Volume, Low Pressure Cuff, REF 112080070
Product Codes/Lot Numbers:
UDI/DI 14026704341266, Batch Numbers: 18FG19, 18GG19, 18HG28, 18IG06, 18IG19, 18JG13, 18JG17, 18KG13, 18LT07, 19BG19, 19CT26, 19DT20, 19ET12, 19ET36, 19HT26, 19HT69, 19JT21, 19KT14, 19LT31, 19LT51, 20AT22, 20AT58, 20BT13, 20BT42, 20CT13, 20DT10, 20ET12, 20FT11, 20FT19, 20GG40, 20GT38, KME20K2577, KME20L1985, KME20M1771, KME20M1772, KME21F1585, KME21J0644, KME21J1078, KME22A1109, KME22A1781, KME22B0401, KME22F1174, KME22F2171, KME22G1295, KME22G2999
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1961-2023
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There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).