AMPLATZ TYPE RENAL DILATOR M0062601000 260-100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2009-04-24 for AMPLATZ TYPE RENAL DILATOR M0062601000 260-100 manufactured by Boston Scientific Corporation.

Event Text Entries

[1094578] It was reported to boston scientific corp that a renal dilator was inspected upon receipt at the user facility. According to the complainant, during unpacking, the internal "slots" that the device is packed in were damaged. There was no damage to the outer packaging and it is unk if the device was damaged. There was no pt involvement in this event.
Patient Sequence No: 1, Text Type: D, B5


[8275388] The device has not been rec'd for analysis. Upon receipt and completion of the failure analysis of the complaint device, if there is any further relevant info from that review, a supplemental mdr will be filed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3005099803-2009-02054
MDR Report Key1437869
Report Source06,07
Date Received2009-04-24
Date of Report2009-03-30
Date of Event2009-03-30
Date Mfgr Received2009-03-30
Device Manufacturer Date2009-02-01
Date Added to Maude2009-09-08
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 ContactCHARLES MONTGOMERY
Manufacturer Street100 BOSTON SCIENTIFIC WAY
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086836132
Manufacturer G1BOSTON SCIENTIFIC CORPORATION
Manufacturer Street780 BROOKSDIE DR.
Manufacturer CitySPENCER IN 47460
Manufacturer CountryUS
Manufacturer Postal Code47460
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAMPLATZ TYPE RENAL DILATOR
Product CodeGCC
Date Received2009-04-24
Model NumberM0062601000
Catalog Number260-100
Lot Number12409412
Device Expiration Date2013-02-17
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer AddressSPENCER IN US


Patients

Patient NumberTreatmentOutcomeDate
10 2009-04-24

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