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Teleflex Medical Europe Ltd recalls RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055
Recalled August 25, 2021 · FDA recall Z-2322-2021 · Teleflex Medical Europe
Hazard
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat. · FDA Class II
Units
638220 units
Sold at
US Nationwide distribution.
Description
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
Product
RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055 c) 112082060 d) 112082065 e) 112082070 f) 112082075 g) 112082080 h) 112082085 i) 112082090 j) 112082095 k) 112082100
Manufacturer(s)
Teleflex Medical Europe Ltd
Made in
Ireland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →