Official recall record

Fresenius Blood Pump Rotor

What the authority reported

This is a field action notification by the manufacturer, Fresenius USA Inc. for Blood Pump Rotor Spare Parts that are compatible with 2008 series hemodialysis machine. The Blood Pump Rotor turns to move the blood along the blood pump segment of the machine. An increased number of complaints were reported to the manufacturer on the Blood Pump Rotor (p/n - f40015481 rev a, implemented in May 2020) after a period of use by clinics noting loose/dislodged guide sheaves. After thorough review of the complaints and root cause investigation, the manufacturer updated the Blood Pump Rotor design to p/n - f40015481 rev c to address customer complaints for bent guide pins due to improper unloading of blood lines. The rev a part was installed as a component of the arterial blood pump on the 2008 series hemodialysis machines during the period May 2020 till Apr 2024. The blood pump rotor is also sold as a spare part for the 2008 series blood pump module. Since, rev c design is now complete, and the part is now available, Fresenius USA has initiated a field action notification to conduct medical device correction if necessary. Recall start date: April 16, 2024

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

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