Skip to content
Recall Observatory FDA recall evidence

Device product

BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating, Product Code 701047554. For use with an extracorporeal cardiovascular or cardiopulmonary bypass circuit.

Z-0977-2024

January 08, 2024

Class II

Product summary

Firm
Maquet Medical Systems USA
Event
Event 93852
Status
Ongoing
Classification
Class II
Quantity
1090 total
Official record key
device-enforcement:Z-0977-2024

Official wording

Reason: Nonconformities at their seal could potentially compromise the sterile barrier for affected products. Breach of sterile barrier could expose patients to pathogenic agents, resulting in the following potential harms: inflammation, infection, or sepsis.

Code information: UDI-DI 4037691530864 Lots 3000286570 and 3000325568 ***Lots added 3/21/24*** 3000341070; 3000355577; 3000358977

Distribution pattern: Worldwide - US Nationwide distribution to the states of CA, IL, MD, MO, NC, NY, OH, OR, PA, TX, UT, VA and the countries of Canada, Germany, Italy, Japan, and Netherlands.

Derived failure modes

  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    sterile barrier for affected products. Breach