Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704341051, Batch Numbers: 18FG12, 18GG26, 18GT26, 18HG24, 18HG36, 18JG13, 18JG36, 18LG31, 18LG33, 19AG11, 19AG21, 19CG07, 19DT42, 19FT18, 19GT43, 19JT02, 19KT37, 19LT32, 20AT13, 20BT53, 20CT21, 20DT15, 20ET50, 20FT36, 20FT60, 20GG43, 20GT40, KME20K2722, KME20K2733, KME20L0659, KME20L1620, KME20M0897, KME20M1522, KME21A0198, KME21A0967, KME21A2397, KME21B2435, KME21C0325, KME22C1814, KME22C1815, KME22C2815, KME22D1075, KME22D3468, KME22E0686, KME22E2786, KME22F1459, KME22G0186, KME22G0338, KME22H1790, KME22J0267, KME22J1449, KME22J2193, KME22J2455, KME22K0574, KME22M1047, KME22M1305, KME22M1323, KME22M2819, KME22M3040, KME23A2332, KME23A2894, KME23A2895, KME23A3034
- 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 111780045
Product Codes/Lot Numbers:
UDI/DI 14026704341051, Batch Numbers: 18FG12, 18GG26, 18GT26, 18HG24, 18HG36, 18JG13, 18JG36, 18LG31, 18LG33, 19AG11, 19AG21, 19CG07, 19DT42, 19FT18, 19GT43, 19JT02, 19KT37, 19LT32, 20AT13, 20BT53, 20CT21, 20DT15, 20ET50, 20FT36, 20FT60, 20GG43, 20GT40, KME20K2722, KME20K2733, KME20L0659, KME20L1620, KME20M0897, KME20M1522, KME21A0198, KME21A0967, KME21A2397, KME21B2435, KME21C0325, KME22C1814, KME22C1815, KME22C2815, KME22D1075, KME22D3468, KME22E0686, KME22E2786, KME22F1459, KME22G0186, KME22G0338, KME22H1790, KME22J0267, KME22J1449, KME22J2193, KME22J2455, KME22K0574, KME22M1047, KME22M1305, KME22M1323, KME22M2819, KME22M3040, KME23A2332, KME23A2894, KME23A2895, KME23A3034
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1942-2023
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