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Alung Technologies Inc recalls ALung Technologies Hemolung Respiratory Assist System (RAS) with CME BodyGuard 323 Infusion Pump(EUA) - Product Usage: a
Recalled February 10, 2021 · FDA recall Z-0938-2021 · Alung Technologies
Hazard
CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a component to the Hemolung for EUA, and the infusion pump may have a delivery inaccuracy · FDA Class II
Units
101 units
Sold at
US Nationwide distribution.
Description
CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a component to the Hemolung for EUA, and the infusion pump may have a delivery inaccuracy
Product
ALung Technologies Hemolung Respiratory Assist System (RAS) with CME BodyGuard 323 Infusion Pump(EUA) - Product Usage: an off-the-shelf infusion pump and administration set to provide a 30 mL/hr continuous saline flush to the integrated blood pump bearing.
Manufacturer(s)
Alung Technologies Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →