TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082065
- Recall date
- May 25, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1887-2023
- FDA classification
- Class I
- Brand / firm
- TELEFLEX LLC
- Sold / distributed
- US Nationwide distribution including Puerto Rico.
Why it was recalled
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082065
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