Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040
Reported: July 5, 2023 Initiated: May 25, 2023 #Z-1863-2023
Product Description
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040
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
- 5120 units
- Distribution
- US Nationwide distribution including Puerto Rico.
- Location
- Morrisville, NC
Frequently Asked Questions
What product was recalled? ▼
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040. Recalled by TELEFLEX LLC. Units affected: 5120 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-1863-2023.
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