Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-00-0800-53, 0998-00-0800-55, 0998-00-0800-65
FDA Recall Z-2615-2021 · Posted None
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Recalling FirmDatascope Corp.
Recall StatusOpen, Classified
Product CodeDSP
Date Initiated2021-09-08
Product Quantity3969 total (US), 3550 total (OUS)
Reason for Recall
The Cardiosave IABP may unexpectedly shut down when the device is running on AC power, only one battery is
installed in the IABP, and the battery is physically removed while the battery is being charged. This occurs during
a very specific set of conditions.
Firm Action
On Wednesday, September 8, 2021, the firm distributed Urgent Medical Device Correction letters to affected customers. Customers were informed that all lots of Maquet Cardiosave Hybrid experience the following issue: Unexpected
Shutdown Upon
Battery Removal.
Immediate Actions to be taken by Customers:
To ensure that the Cardiosave Hybrid is not susceptible to shutdown during the removal of a battery, users should not eject a battery when:
- There is a singulat battery in either battery charging bay and unused battery bay is empty.
- The battery is charging on AC power (indicated by a flashing LED on the battery pack).
Additionally, the user can prevent the issue by ensuring that a battery is inserted into each of
the two battery bays. Should a charging battery be ejected inadvertently, the unit will
automatically switch over to the second battery, thus preventing system shutdown.
Furthermore, Datascope/Getinge is developing a software correction to address this issue. A
Datascope/Getinge service representative will contact you to schedule the installation of the
updated software. This work will be done at no cost to your facility.
If you have
any questions, please contact your Datascope/Getinge representative or call the
Datascope/Getinge Technical Support at 1-888-943-8872, options 4, 2, 1, Monday through
Friday, between the hours of 8:00 a.m. and 6:00 p.m. (Eastern Time Zone).
Root Cause
Software design
Distribution Pattern
Nationwide domestic distribution. Foreign distribution worldwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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