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OptumHealth Care Solutions LLC recalls Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump
Recalled May 29, 2024 · FDA recall Z-1811-2024 · OptumHealth Care Solutions
Hazard
Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being removed the from the market due to multiple potential failure modes, including battery failure, upstream occlusion, system errors, drug product leakage, high or low flow rate, or damaged pump housing. · FDA Class I
Units
208 units
Sold at
US Nationwide Distribution
Description
Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being removed the from the market due to multiple potential failure modes, including battery failure, upstream occlusion, system errors, drug product leakage, high or low flow rate, or damaged pump housing.
Product
Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump
Manufacturer(s)
OptumHealth Care Solutions LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →