Public recall detail

Fresenius Blood Pump Rotor

2024-05-06

medium
Recall Safety notice
Quick summary

Quick summary: Fresenius Blood Pump Rotor. Date: 2024-05-06.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Fresenius Blood Pump Rotor. Date: 2024-05-06.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandFresenius USA, Inc.
ProductFresenius Blood Pump Rotor
IssueMedical devices - Performance
Recall classType II
IdentificationRA-75480

Affected products

ProductAffected products
LotLot or serial number
ModelModel or catalog number/
Serial numberLot or serial number
DescriptionAffected products
ProductBlood Pump Rotor (Spare Part) Used For Fresenius 2008T Hemodialysis System
LotNot applicable.
Model190729
Serial numberNot applicable.
DescriptionBlood Pump Rotor (Spare Part) Used For Fresenius 2008T Hemodialysis System
ProductBlood Pump Rotor (Spare Part) Used For K@Home
LotNot applicable.
Model191014 190395
Serial numberNot applicable.
DescriptionBlood Pump Rotor (Spare Part) Used For K@Home
ProductBlood Pump Rotor (Spare Part) Used For 2008T Hemodialysis System CDX
LotNot applicable.
Model190713 190766 190908 190573
Serial numberNot applicable.
DescriptionBlood Pump Rotor (Spare Part) Used For 2008T Hemodialysis System CDX

Issue

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 you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Gastroenterology and urology
CompaniesFresenius USA, Inc. 4040 Nelson Avenue, Concord, California, United States, 94520
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-75480
Background{}
CompaniesFresenius USA, Inc. 4040 Nelson Avenue, Concord, California, United States, 94520
AudiencesHealthcare
Source updated2024-05-06

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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