Datascope Corp. Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
Brand
Datascope Corp.
Lot Codes / Batch Numbers
All lots
Products Sold
All lots
Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-75, 0998-00-0800-83, 099 due to The Helium Indicator on the Cardiosave display may over represent the amount of helium in unit in the presence of Electromagnetic Interference.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Helium Indicator on the Cardiosave display may over represent the amount of helium in unit in the presence of Electromagnetic Interference.
Recommended Action
Per FDA guidance
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 and Maquet Cardiosave Rescue experience the following issue: Helium Indicator Inaccuracy in the Presence of Continuous EMC Disturbances. Customers were provided with actions to take to limit the possibility of loss of therapy due to an over-reporting of remaining helium on the Helium Indicator. Cardiosave Hybrid users should view the mechanical gauge on the Cardiosave Top Panel to assess remaining helium capacity in case of suspected EMC disturbances. Cardiosave Rescue users should ensure the internal helium reservoir is full prior to use of the device. If the on-screen helium indicator is not showing full, fill the internal helium reservoir via the hospital cart or Helium Refilling Station. Please review the Cardiosave IABP Operation Transport Quick Reference Guide (0002-08-9772) for details on using the Cardiosave Rescue in transport. For both devices: Where practical maximize separation of Cardiosave system from other electronic equipment, communication devices and cables (e.g. power and communication cables). In particular, follow the recommended separation distances between communications equipment and the Cardiosave equipment as specified in the Cardiosave Operating instructions manual. The firm is developing a hardware correction to address this issue. A Datascope/Getinge service representative will contact customers to schedule the installation of the correction when available. The correction approximately will begin late Q2 2022. 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).
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026