COUNTERSINK, CANNULATED AUTOFIX 2.0/2.5 9071003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-12-28 for COUNTERSINK, CANNULATED AUTOFIX 2.0/2.5 9071003 manufactured by Stryker Gmbh.

Event Text Entries

[35017233] (b)(4). Device will not be returned. If additional information becomes available it will be provided on a supplemental report. The device is not available to stryker.
Patient Sequence No: 1, Text Type: N, H10


[35017234] T-7 driver and countersink broke during surgery.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008031020-2015-00676
MDR Report Key5328833
Date Received2015-12-28
Date of Report2014-05-28
Date of Event2014-05-28
Date Mfgr Received2014-05-28
Date Added to Maude2015-12-28
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 ContactMR. ANNA JUSINSKI
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer Phone2018315000
Manufacturer G1STRYKER GMBH
Manufacturer StreetBOHNACKERWEG 1 POSTFACH
Manufacturer CitySELZACH 2545
Manufacturer CountryCH
Manufacturer Postal Code2545
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCOUNTERSINK, CANNULATED AUTOFIX 2.0/2.5
Generic NameORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Product CodeHWW
Date Received2015-12-28
Catalog Number9071003
Lot NumberV0498
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER GMBH
Manufacturer AddressBOHNACKERWEG 1 POSTFACH SELZACH 2545 CH 2545


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-12-28

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