PlainRecalls
FDA Devices Moderate Class II Ongoing

Blood Pump Rotor, Model Number: F40015481 Rev A

Reported: May 29, 2024 Initiated: April 17, 2024 #Z-1866-2024

Product Description

Blood Pump Rotor, Model Number: F40015481 Rev A

Reason for Recall

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

Details

Units Affected
45,880 components
Distribution
US Nationwide distribution.
Location
Waltham, MA

Frequently Asked Questions

What product was recalled?
Blood Pump Rotor, Model Number: F40015481 Rev A. Recalled by Fresenius Medical Care Holdings, Inc.. Units affected: 45,880 components.
Why was this product recalled?
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 29, 2024. Severity: Moderate. Recall number: Z-1866-2024.