ELECTRICAL UMBILICAL CABLE 2035U

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-10-27 for ELECTRICAL UMBILICAL CABLE 2035U manufactured by Medtronic Cryocath Lp.

Event Text Entries

[29932359] This event occurred outside the us where the same model is distributed. All information provided is included in this report. Patient information is not generally available due to confidentiality concerns. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[29932360] It was reported that prior to use, there were four electrical cables in one package and no inner or sterile packing. It was noted that the packing box was sealed with a sticker and the orientation of the sticker was observed to be positioned differently than expected. The cables were not replaced and no patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


[37031721]
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3002648230-2015-00368
MDR Report Key5180094
Date Received2015-10-27
Date of Report2015-10-02
Date of Event2015-10-02
Date Mfgr Received2015-10-02
Device Manufacturer Date2012-04-24
Date Added to Maude2015-10-27
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 ContactANNE SCHILLING
Manufacturer Street8200 CORAL SEA ST NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone7635052036
Manufacturer G1MEDTRONIC CARDIAC RHYTHM HEART FAILURE
Manufacturer Street8200 CORAL SEA ST NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal Code55112
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameELECTRICAL UMBILICAL CABLE
Generic NameCABLE
Product CodeISN
Date Received2015-10-27
Model Number2035U
Catalog Number2035U
Lot Number09352
Device Expiration Date2014-03-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC CRYOCATH LP
Manufacturer Address16771 CHEMIN STE-MARIE KIRKLAND H9H 5H3 CA H9H 5H3


Patients

Patient NumberTreatmentOutcomeDate
10 2015-10-27

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