CS300 N/A 0998-00-3023-53

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-27 for CS300 N/A 0998-00-3023-53 manufactured by Datascope Corp. - Mahwah.

Event Text Entries

[185521945] The production device history record (dhr) for this intra-aortic balloon pump (iabp) was not required to be reviewed as per company standard operating procedure since the device manufacture date is greater than one year from the event date. A getinge service territory manager (stm) was dispatched to evaluate the iabp unit. The batteries were not replaced. A preventative maintenance (pm) was completed. The stm completed all safety, functionality and calibration checks and all tests passed to factory specifications. The iabp unit was cleared for clinical use and released to the customer.
Patient Sequence No: 1, Text Type: N, H10


[185521946] It was reported that, before use on a patient, the cs300 intra-aortic balloon pump (iabp) had a battery replacement error. There was no patient involvement, thus no adverse event was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2249723-2020-00514
MDR Report Key9889944
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-03-27
Date of Report2020-03-24
Date of Event2020-03-05
Date Mfgr Received2020-03-05
Device Manufacturer Date2007-02-01
Date Added to Maude2020-03-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street1300 MACARTHUR BLVD
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer G1DATASCOPE CORP. - MAHWAH
Manufacturer Street1300 MACARTHUR BLVD
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal Code07430
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCS300
Generic NameSYSTEM, BALLOON, INTRA-AORTIC AND CONTROL
Product CodeDSP
Date Received2020-03-27
Model NumberN/A
Catalog Number0998-00-3023-53
Lot NumberN/A
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDATASCOPE CORP. - MAHWAH
Manufacturer Address1300 MACARTHUR BLVD MAHWAH NJ 07430 US 07430


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-27

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