Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704341242, Batch Numbers: 18GG18, 18HG21, 18IG16, 18KG01, 18KG19, 18LG18, 19BG18, 19BG33, 19GT13, 19HT31, 19HT55, 19IT15, 19JT35, 19KT14, 19LT21, 20AT26, 20CT11, 20FT68, 20GT49, KME20M0409, KME21A1111, KME21A2095, KME21B2212, KME21C2483, KME21C3405, KME22B0921, KME22B0923, KME22D0289, KME22D1811, KME22D1855, KME22D2401, KME22E2898, KME22H2600, KME22H3295, KME22J2877, KME22K2861, KME22K3117, KME22M1510, KME22M2546, KME23B0521, KME23B3047
- 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 111781080
Product Codes/Lot Numbers:
UDI/DI 14026704341242, Batch Numbers: 18GG18, 18HG21, 18IG16, 18KG01, 18KG19, 18LG18, 19BG18, 19BG33, 19GT13, 19HT31, 19HT55, 19IT15, 19JT35, 19KT14, 19LT21, 20AT26, 20CT11, 20FT68, 20GT49, KME20M0409, KME21A1111, KME21A2095, KME21B2212, KME21C2483, KME21C3405, KME22B0921, KME22B0923, KME22D0289, KME22D1811, KME22D1855, KME22D2401, KME22E2898, KME22H2600, KME22H3295, KME22J2877, KME22K2861, KME22K3117, KME22M1510, KME22M2546, KME23B0521, KME23B3047
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1957-2023
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