Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780070
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704341105, Batch Numbers: 18FG12, 18FG24, 18GG01, 18GG26, 18GT26, 18HG36, 18IG14, 18IT05, 18JG07, 18KG10, 18KG34, 18LG11, 18LG31, 19AG36, 19CG07, 19CT69, 19ET12, 19GT39, 19GT44, 19HT80, 19IT12, 19IT43, 19JT01, 19JT55, 19KT21, 19LT08, 19LT31, 20AT13, 20AT49, 20BT53, 20CT24, 20DT09, 20DT24, 20ET50, 20FT39, 20FT59, 20GG27, KME20J2813, KME20J3155, KME20K1111, KME20K2068, KME20K3244, KME20L0730, KME20L0731, KME20L1681, KME20M0276, KME20M0955, KME20M2655, KME21A0979, KME21B0096, KME21B0154, KME21B1518, KME21C0334, KME21M1046, KME22A0450, KME22A1594, KME22B0425, KME22B1002, KME22C0473, KME22D1110, KME22D2351, KME22D2363, KME22D3366, KME22D3379, KME22E1102, KME22E2443, KME22F1333, KME22G0171, KME22G1728, KME22G3156, KME22H0815, KME22H1321, KME22J0749, KME22K1286, KME22K2440, KME22L1550, KME22L1660, KME22L2544
- 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:
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780070
Product Codes/Lot Numbers:
UDI/DI 14026704341105, Batch Numbers: 18FG12, 18FG24, 18GG01, 18GG26, 18GT26, 18HG36, 18IG14, 18IT05, 18JG07, 18KG10, 18KG34, 18LG11, 18LG31, 19AG36, 19CG07, 19CT69, 19ET12, 19GT39, 19GT44, 19HT80, 19IT12, 19IT43, 19JT01, 19JT55, 19KT21, 19LT08, 19LT31, 20AT13, 20AT49, 20BT53, 20CT24, 20DT09, 20DT24, 20ET50, 20FT39, 20FT59, 20GG27, KME20J2813, KME20J3155, KME20K1111, KME20K2068, KME20K3244, KME20L0730, KME20L0731, KME20L1681, KME20M0276, KME20M0955, KME20M2655, KME21A0979, KME21B0096, KME21B0154, KME21B1518, KME21C0334, KME21M1046, KME22A0450, KME22A1594, KME22B0425, KME22B1002, KME22C0473, KME22D1110, KME22D2351, KME22D2363, KME22D3366, KME22D3379, KME22E1102, KME22E2443, KME22F1333, KME22G0171, KME22G1728, KME22G3156, KME22H0815, KME22H1321, KME22J0749, KME22K1286, KME22K2440, KME22L1550, KME22L1660, KME22L2544
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1947-2023
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