Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080
Reported: July 5, 2023 Initiated: May 25, 2023 #Z-1890-2023
Product Description
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080
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
- 170179 units
- Distribution
- US Nationwide distribution including Puerto Rico.
- Location
- Morrisville, NC
Frequently Asked Questions
What product was recalled? ▼
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080. Recalled by TELEFLEX LLC. Units affected: 170179 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-1890-2023.
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