Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704341389, Batch Numbers: 18GG02, 18GG19, 18GG23, 18GT06, 18JG04, 18JG15, 18JG16, 18JG18, 18JT06, 18JT16, 19AG33, 19AT20, 19BG02, 19BG03, 19BG10, 19BG15, 19BG22, 19BG26, 19BG42, 19BT04, 19CT25, 19CT82, 19DT05, 19FT38, 19IT26, 19JT18, 19LT13, 19LT17, 19LT50, 20AT13, 20AT40, 20BT38, 20CT02, 20CT12, 20CT43, 20DT13, 20ET12, 20ET17, 20ET56, 20FT23, 20GG47, 20GT32, KME20J1385, KME21G1704, KME21G1949, KME21K0151, KME21K0292, KME21M2075, KME21M2306, KME21M2649, KME22A1589, KME22A2197, KME22B1848, KME22B2478, KME22B2538, KME22B2578, KME22B2692, KME22C0066, KME22C0571, KME22D0281, KME22D2503, KME22D2504, KME22E0316, KME22E1277, KME22E1422, KME22E2743, KME22E2879, KME22G0063, KME22J0616, KME22J1331, KME22J1463, KME22K0660, KME22L1657, KME23A2133, KME23A2214, KME23A2221, KME23A2299, KME23A2358, KME23C0172
- 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 112082050
Product Codes/Lot Numbers:
UDI/DI 14026704341389, Batch Numbers: 18GG02, 18GG19, 18GG23, 18GT06, 18JG04, 18JG15, 18JG16, 18JG18, 18JT06, 18JT16, 19AG33, 19AT20, 19BG02, 19BG03, 19BG10, 19BG15, 19BG22, 19BG26, 19BG42, 19BT04, 19CT25, 19CT82, 19DT05, 19FT38, 19IT26, 19JT18, 19LT13, 19LT17, 19LT50, 20AT13, 20AT40, 20BT38, 20CT02, 20CT12, 20CT43, 20DT13, 20ET12, 20ET17, 20ET56, 20FT23, 20GG47, 20GT32, KME20J1385, KME21G1704, KME21G1949, KME21K0151, KME21K0292, KME21M2075, KME21M2306, KME21M2649, KME22A1589, KME22A2197, KME22B1848, KME22B2478, KME22B2538, KME22B2578, KME22B2692, KME22C0066, KME22C0571, KME22D0281, KME22D2503, KME22D2504, KME22E0316, KME22E1277, KME22E1422, KME22E2743, KME22E2879, KME22G0063, KME22J0616, KME22J1331, KME22J1463, KME22K0660, KME22L1657, KME23A2133, KME23A2214, KME23A2221, KME23A2299, KME23A2358, KME23C0172
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1884-2023
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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).