FDA Medical Device Recalls (openFDA)
Datascope Corp.: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
- Recall number
- Z-0076-2022
- Recalling firm
- Datascope Corp.
- Product
- Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
- Status
- Open, Classified
- Initiated
- 2021-09-08
- Posted
- 2021-10-07
- Terminated
- not on file
- Reason
- The Helium Indicator on the Cardiosave display may over represent the amount of helium in unit in the presence of Electromagnetic Interference.
- Root cause
- Device Design
- 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 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).
- Quantity
- 5054 total (US); 5033 total (OUS)
- Distribution
- Worldwide distribution - US Nationwide distribution.
- Lot, serial or model codes
- All lots
- 510(k) numbers
- ["K181122"]
- PMA numbers
- not on file
- Product code
- DSP
- Firm FEI
- 3001418283
- Firm city
- Mahwah
- Firm state
- NJ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28