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FDA Medical Device Recalls (openFDA)

Datascope Corp.: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-0800-55, 0998-UC-0800-55, 0998-00-0800-65

Recall number
Z-2437-2023
Recalling firm
Datascope Corp.
Product
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-0800-55, 0998-UC-0800-55, 0998-00-0800-65
Status
Open, Classified
Initiated
2023-07-31
Posted
2023-08-30
Terminated
not on file
Reason
Users were identifying autofill failure conditions on the devices causing pump stops.
Root cause
Under Investigation by firm
Action
An URGENT MEDICAL DEVICE CORRECTION dated 7/31/23 was sent to customers. Autofill Alarms User Actions to be taken now: Our records indicate that you may have a Cardiosave Hybrid and/or Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) in your facility. Please examine your inventory immediately to determine if you have any Cardiosave Hybrid and/or Rescue IABPs. As a result of the investigation into the complaints, Getinge would like to reinforce information that is detailed in the Cardiosave Instructions for Use to help minimize the frequency and impact of these alarms: As per the Cardiosave Operating Instructions in sections 2.1.8, Initiation of Assist and 2.1.9, IAB Fill ; the system performs an autofill under the following three conditions: " Initiation of Therapy " Every two (2) hours while therapy is ongoing " If during transport, the atmospheric pressure changes by a 25 mmHg (~1,000 ft.) rise or 50 mmHg (~2,000 ft.) drop during therapy to keep the balloon pressure acclimated to local conditions If the autofill procedure fails to purge and fill the Pneumatic Module properly, the message Autofill Failure will be displayed, an audible alarm will be activated, and pumping will be suspended until the alarm is cleared. Corrective action can be obtained by pressing the Help Available key. The three high priority alarms are: " Autofill Failure No Helium " Autofill Failure Blood Suspected " Autofill Failure Note: Autofill Failure Blood Suspected is caused by a leak in the IAB which results in blood migration back into the IABP system. The failure of the IAB is outside of the scope of this Field Safety Notification. Autofill Failure No Helium " Verify that the Cardiosave device has sufficient Helium in the system. " If the Cardiosave is in Hybrid mode (console within a hospital cart), verify the external Helium Tank is connected to the cart, is opened, and there is sufficient Helium in the tank to support the IABP therapy. " If the Cardiosave is in Rescue
Quantity
9175 units
Distribution
Worldwide - US Nationwide distribution.
Lot, serial or model codes
All Lot Numbers. Model: 0998-00-0800-31, UDI: 10607567109053; Model: 0998-UC-0800-31, UDI: N/A; Model: 0998-00-0800-32, UDI: 10607567111117; Model: 0998-00-0800-33, UDI: 10607567109008; Model: 0998-UC-0800-33, UDI: N/A; Model: 0998-00-0800-34, UDI: 10607567111940; Model: 0998-00-0800-35, UDI: 10607567109107; Model: 0998-00-0800-45, UDI: 10607567108421; Model: 0998-00-0800-52, UDI: 10607567108438; Model: 0998-UC-0800-52, UDI: N/A; Model: 0998-00-0800-53, UDI: 10607567108391; Model: 0998-UC-0800-53, UDI: N/A; Model: 0998-00-0800-55, UDI: 10607567108414; Model: 0998-UC-0800-55, UDI: N/A; Model: 0998-00-0800-65, UDI: 10607567113432; Model: 0998-00-0800-75, UDI: 10607567112312; Model: 0998-00-0800-83, UDI: 10607567108407; Model: 0998-00-0800-85, UDI: 10607567113449
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

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