Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704340832, Batch Numbers: 18FG02, 18FT26, 18FT35, 18GG26, 18HT18, 18IG04, 18IG10, 18JG36, 18JT06, 18JT10, 18KG23, 18KT30, 18LG06, 18LT18, 19BG16, 19BG21, 19CG06, 19DT16, 19DT39, 19GT58, 19IT20, 19JT46, 19KT29, 19LT46, 20AT26, 20CT11, 20CT38, 20DT13, 20DT23, 20GG45, 20GT24, 20GT41, 20GT44, KME20H0293, KME20H1490, KME20H2049, KME20L1755, KME20L2383, KME20L2596, KME20M2056, KME21M2476, KME22A1524, KME22D0857, KME22D2479, KME22D3022, KME22F2427, KME22G0200, KME22G1191
- 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 uncuffed/plain - Murphy, REF 100382050
Product Codes/Lot Numbers:
UDI/DI 14026704340832, Batch Numbers: 18FG02, 18FT26, 18FT35, 18GG26, 18HT18, 18IG04, 18IG10, 18JG36, 18JT06, 18JT10, 18KG23, 18KT30, 18LG06, 18LT18, 19BG16, 19BG21, 19CG06, 19DT16, 19DT39, 19GT58, 19IT20, 19JT46, 19KT29, 19LT46, 20AT26, 20CT11, 20CT38, 20DT13, 20DT23, 20GG45, 20GT24, 20GT41, 20GT44, KME20H0293, KME20H1490, KME20H2049, KME20L1755, KME20L2383, KME20L2596, KME20M2056, KME21M2476, KME22A1524, KME22D0857, KME22D2479, KME22D3022, KME22F2427, KME22G0200, KME22G1191
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1876-2023
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).