DIRECTINJECT ON DEMAND HA CEMENT 79-45905

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-11-29 for DIRECTINJECT ON DEMAND HA CEMENT 79-45905 manufactured by Stryker Orthopaedics-cork.

Event Text Entries

[61301686] Device is not available for evaluation. If additional information is received it will be reported on a supplemental report.
Patient Sequence No: 1, Text Type: N, H10


[61301687] A sales representative reported that the syringe tip had broken off of the direct inject canula. There was no adverse consequences, delay in surgery, or medical intervention reported for this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008010177-2016-00281
MDR Report Key6131956
Date Received2016-11-29
Date of Report2016-11-08
Date of Event2016-11-07
Date Mfgr Received2016-11-08
Date Added to Maude2016-11-29
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. HANS GEIGER
Manufacturer StreetBOETZINGERSTR. 41
Manufacturer CityFREIBURG D-79111
Manufacturer PostalD-79111
Manufacturer Phone76145120
Manufacturer G1STRYKER ORTHOPAEDICS-CORK
Manufacturer StreetIDA INDUSTRIAL ESTATE
Manufacturer CityCARRIGTWOHILL NA
Manufacturer Postal CodeNA
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameDIRECTINJECT ON DEMAND HA CEMENT
Generic NameIMPLANT
Product CodeGXP
Date Received2016-11-29
Catalog Number79-45905
Lot Number16104
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ORTHOPAEDICS-CORK
Manufacturer AddressIDA INDUSTRIAL ESTATE CARRIGTWOHILL NA NA


Patients

Patient NumberTreatmentOutcomeDate
10 2016-11-29

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