Medtronic Perfusion Systems: Medical Device Recalls in 2014

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Medtronic Perfusion Systems in 2014. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

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The Affinity Fusion Oxygenator with Integrated Arterial Filter and Carmeda Bioactive Surface is a single-use, microporous, hollow-fiber, gas-exchange device with plasma resistant fiber and integrated heat exchanger and arterial filter. The oxygenator is bonded on its primary blood contacting surfaces with a non-leaching biocompatible surface to reduce platelet activation and adhesion and preserve platelet function. The device is non-toxic, nonpyrogenic, and supplied sterile in individual packaging.