MICRO-PACE 4570

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 MICRO-PACE 4570 manufactured by Pace Medical, Inc.

Event Text Entries

[2862476] Pace medical was notified on 09/09/2011 by (b)(6) via letter that unit had a fault.
Patient Sequence No: 1, Text Type: D, B5


[10223468] Customer returned device stating a complaint that it was not pacing appropriately. The device was examined and no faults could be found. Device functioned normally. The device was tested 24 hours and functioned as designed. Device re-calibrated and final tested. All tests were passed and the device was returned to the customer. Reason for complaint: user error.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1218087-2012-00050
MDR Report Key2699213
Report Source01,07
Date Received2012-08-13
Date Mfgr Received2011-09-14
Device Manufacturer Date1998-05-01
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 ST, STE 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 NameMICRO-PACE
Generic NameTEMPORARY CARDIAC PACEMAKER
Product CodeJOQ
Date Received2012-08-13
Returned To Mfg2011-09-09
Model Number4570
Catalog Number4570
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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