Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035
Reported: July 5, 2023 Initiated: May 25, 2023 #Z-1940-2023
Product Description
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035
Reason for Recall
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Details
- Recalling Firm
- TELEFLEX LLC
- Units Affected
- 36135 units
- Distribution
- US Nationwide distribution including Puerto Rico.
- Location
- Morrisville, NC
Frequently Asked Questions
What product was recalled? ▼
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035. Recalled by TELEFLEX LLC. Units affected: 36135 units.
Why was this product recalled? ▼
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 5, 2023. Severity: Critical. Recall number: Z-1940-2023.
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