Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704341464, Batch Numbers: 18FG23, 18FT17, 18FT24, 18FT25, 18FT49, 18GG12, 18GG26, 18JG38, 18KG04, 18KG05, 18KG23, 18KG26, 18KG38, 18KT04, 18KT27, 18LG13, 19AT19, 19CG02, 19ET11, 19JT61, 19KT35, 19LT35, 19LT46, 20AT57, 20BT38, 20DT28, KME20H0415, KME20H2140, KME20H2314, KME20H2913, KME20J1999, KME20K0212, KME20K0600, KME20K1434, KME20K3525, KME20L0805, KME21K0478, KME21L1274, KME21L1371, KME22A2199, KME22A2286, KME22A2317, KME22B1140, KME22B1997, KME22B2180, KME22C0133, KME22C0202, KME22C0454, KME22C0573, KME22C0675, KME22D3492, KME22E1281, KME22E1282, KME22E2749, KME22F2444, KME22H2380, KME22K0996, KME23A2734, KME23B2546
- 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 Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090
Product Codes/Lot Numbers:
UDI/DI 14026704341464, Batch Numbers: 18FG23, 18FT17, 18FT24, 18FT25, 18FT49, 18GG12, 18GG26, 18JG38, 18KG04, 18KG05, 18KG23, 18KG26, 18KG38, 18KT04, 18KT27, 18LG13, 19AT19, 19CG02, 19ET11, 19JT61, 19KT35, 19LT35, 19LT46, 20AT57, 20BT38, 20DT28, KME20H0415, KME20H2140, KME20H2314, KME20H2913, KME20J1999, KME20K0212, KME20K0600, KME20K1434, KME20K3525, KME20L0805, KME21K0478, KME21L1274, KME21L1371, KME22A2199, KME22A2286, KME22A2317, KME22B1140, KME22B1997, KME22B2180, KME22C0133, KME22C0202, KME22C0454, KME22C0573, KME22C0675, KME22D3492, KME22E1281, KME22E1282, KME22E2749, KME22F2444, KME22H2380, KME22K0996, KME23A2734, KME23B2546
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1892-2023
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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).
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).