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CS100 Intra-Aortic Balloon Pump, Refurbished, ITALIAN,NON-UTS,INTL 0998-UC-3013-67Recalls & reported problems

Datascope Corp. · CS100 Intra-Aortic Balloon Pump, Refurbished, ITALIAN,NON-UTS,INTL · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10607567108681), received between Nov 20, 2020 and Nov 19, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Display or Visual Feedback Problem” (1 report).

8 other recalls cover devices cleared under the same FDA submission (K031636); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Display or Visual Feedback Problem1
  • Gas/Air Leak1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 19, 2021Gas/Air Leak; Gas/Air Leak

    IT WAS REPORTED THAT BEFORE USE THE CS100 INTRA-AORTIC BALLOON PUMP (IABP) HAD A HELIUM LEAK. THERE WAS NO PATIENT INVOLVED AND NO ADVERSE EVENT WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12843023 ↗
  • MalfunctionNov 20, 2020Display or Visual Feedback Problem; Display or Visual Feedback Problem

    IT WAS REPORTED THAT THE CS100 INTRA-AORTIC BALLOON PUMP (IABP) HAD A DISPLAY FAULT. IT IS UNKNOWN THE CIRCUMSTANCES UNDER WHICH THE EVENT OCCURRED. IT IS ALSO UNKNOWN IF THERE WAS PATIENT INVOLVEMENT. HOWEVER, THERE WAS NO ADVERSE EVENT REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10877568 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K031636. One submission often covers many models, so check the product and lot details in each record.

  • Z-1486-2026 · Jan 23, 2026 · Open, Classified
    CS100 IABP. Software Version CS100 IABP Q.01.
  • Z-3085-2017 · Jul 17, 2017 · Open, Classified
    CS 100i Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing coronary perfusion and reducing left ventricular work. Coronary perfusion is increased by a
  • Z-3086-2017 · Jul 17, 2017 · Open, Classified
    CS 100 Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing coronary perfusion and reducing left ventricular work. Coronary perfusion is increased by au
  • Z-2736-2017 · Jun 16, 2017 · Terminated
    CS 100i Intra-Aortic Balloon Pump
  • Z-2737-2017 · Jun 16, 2017 · Terminated
    CS 100 Intra-Aortic Balloon Pump
  • Z-1523-2014 · Mar 21, 2014 · Terminated
    Datascope System 98/98xt, CS 100/CS100i and CS 300 Intra-Aortic Balloon Pump. The Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate in
  • Z-2414-2011 · Mar 16, 2011 · Terminated
    Datascope/ Maquet IABPs. System 98/98XT Intra-Aortic Balloon Pump; CS100/CS100i Intra-Aortic Balloon Pump; CS300 Intra-Aortic Balloon Pump; Manufactured by Datascope Corp., 130
  • Z-1811-2010 · May 10, 2010 · Terminated
    CS100 Intra-Aortic Balloon Pump.

Other System, Balloon, Intra-Aortic And Control devices

All System, Balloon, Intra-Aortic And Control devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page