BEDSIDE 4170

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 BEDSIDE 4170 manufactured by Pace Medical, Inc..

Event Text Entries

[2861425] Pace medical was notified on may 26, 2011 by (b)(6) via letter that unit had a fault.
Patient Sequence No: 1, Text Type: D, B5


[10127579] Customer returned device with request to check the pt cable connector. Device was examined and it was found that a component needed to be replaced. The device was re-calibrated and final tested. All tests were passed and the device was returned to the customer. Reason for failure: random component failure.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1218087-2012-00030
MDR Report Key2699090
Report Source01,07
Date Received2012-08-13
Date Mfgr Received2011-06-02
Device Manufacturer Date2002-11-01
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
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 NameBEDSIDE
Generic NameTEMPORARY CARDIAC PACEMAKER
Product CodeJOQ
Date Received2012-08-13
Returned To Mfg2011-05-26
Model Number4170
Catalog Number4170
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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