Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704340863, Batch Numbers: 18KG25, 19BT19, 19CT22, 19CT39, 19ET06, KME21L2054, KME22A2341, KME22C2640, KME22E2541, KME22F1554, KME22F2582
- 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 100382065
Product Codes/Lot Numbers:
UDI/DI 14026704340863, Batch Numbers: 18KG25, 19BT19, 19CT22, 19CT39, 19ET06, KME21L2054, KME22A2341, KME22C2640, KME22E2541, KME22F1554, KME22F2582
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1939-2023
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