ACCUPACE 4802

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2012-08-13 for ACCUPACE 4802 manufactured by Pace Medical, Inc..

Event Text Entries

[2861057] Pace medical was notified on may 19, 2011 by (b)(6) via letter that unit had a fault.
Patient Sequence No: 1, Text Type: D, B5


[10221750] Customer complained that the device was not sensing in the vvi mode. Customer's complaint was confirmed. The analog board was replaced as part of the system's electronic module. The device was re-calibrated and final tested. All tests were passed and the device was returned to the customer. Reason for failure: unknown: possible trace failure in the printed circuit board. This may have been caused by a sudden impact.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1218087-2012-00028
MDR Report Key2699092
Report Source01,07
Date Received2012-08-13
Date Added to Maude2012-08-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer Street310 SOUTH STREET SUITE 2
Manufacturer CityPLAINVILLE MA 02762
Manufacturer CountryUS
Manufacturer Postal02762
Manufacturer Phone5083163861
Single Use3
Remedial ActionRP
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameACCUPACE
Generic NamePACING ANALYZER
Product CodeJOQ
Date Received2012-08-13
Returned To Mfg2011-05-19
Model Number4802
Catalog Number4802
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerPACE MEDICAL, INC.
Manufacturer AddressPLAINVILLE MA 02762 US 02762


Patients

Patient NumberTreatmentOutcomeDate
10 2012-08-13

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