Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781070
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704341228, Batch Numbers: 18GG17, 18GG25, 18GT32, 18HG19, 18IG16, 18JG13, 18JG21, 18KG01, 18LG12, 18LG15, 18LG30, 19AG15, 19AG25, 19AG29, 19BG03, 19CT56, 19GT17, 19HT02, 19HT31, 19HT68, 19HT69, 19IT19, 19JT11, 19JT35, 19KT02, 19LT21, 20AT22, 20BG11, 20CT11, 20DT22, 20DT35, 20FT64, 20FT68, 20GT34, 20GT49, KME20H0436, KME20H2683, KME20M0445, KME20M2650, KME21A2042, KME21A2083, KME21A2187, KME21A2929, KME21B0718, KME21B1715, KME21B1946, KME21C0552, KME21C1043, KME21C1044, KME21C1910, KME21C1912, KME21F1682, KME21F1864, KME21K1635, KME21M0798, KME21M2432, KME22A0810, KME22A2177, KME22A2883, KME22A2924, KME22A3263, KME22B2796, KME22C0042, KME22C0206, KME22C0505, KME22D2264, KME22D3154, KME22E1996, KME22E2224, KME22E2513, KME22F0202, KME22H0792, KME22H1588, KME22H2923, KME22J1124, KME22J2482, KME22J3020
- 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 111781070
Product Codes/Lot Numbers:
UDI/DI 14026704341228, Batch Numbers: 18GG17, 18GG25, 18GT32, 18HG19, 18IG16, 18JG13, 18JG21, 18KG01, 18LG12, 18LG15, 18LG30, 19AG15, 19AG25, 19AG29, 19BG03, 19CT56, 19GT17, 19HT02, 19HT31, 19HT68, 19HT69, 19IT19, 19JT11, 19JT35, 19KT02, 19LT21, 20AT22, 20BG11, 20CT11, 20DT22, 20DT35, 20FT64, 20FT68, 20GT34, 20GT49, KME20H0436, KME20H2683, KME20M0445, KME20M2650, KME21A2042, KME21A2083, KME21A2187, KME21A2929, KME21B0718, KME21B1715, KME21B1946, KME21C0552, KME21C1043, KME21C1044, KME21C1910, KME21C1912, KME21F1682, KME21F1864, KME21K1635, KME21M0798, KME21M2432, KME22A0810, KME22A2177, KME22A2883, KME22A2924, KME22A3263, KME22B2796, KME22C0042, KME22C0206, KME22C0505, KME22D2264, KME22D3154, KME22E1996, KME22E2224, KME22E2513, KME22F0202, KME22H0792, KME22H1588, KME22H2923, KME22J1124, KME22J2482, KME22J3020
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1956-2023
Related Recalls
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).