HYDROSET INJECTABLE CEMENT KIT 10CC 397010

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-06-05 for HYDROSET INJECTABLE CEMENT KIT 10CC 397010 manufactured by Stryker Orthopaedics-limerick.

Event Text Entries

[76765057] Device is not available for evaluation. If additional information is received it will be reported on a supplemental report. Remains implanted.
Patient Sequence No: 1, Text Type: N, H10


[76765058] It was reported by the patient's mother that the patient is experiencing pain after hydroset was used in a procedure. There was no delay in surgery or medical intervention reported regarding this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008010177-2017-00122
MDR Report Key6610808
Date Received2017-06-05
Date of Report2017-06-05
Date of Event2017-05-09
Date Mfgr Received2017-05-09
Date Added to Maude2017-06-05
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 StreetRAHEEN BUSINESS PARK
Manufacturer CityLIMERICK NA
Manufacturer PostalNA
Manufacturer Phone61498200
Manufacturer G1STRYKER ORTHOPAEDICS-LIMERICK
Manufacturer StreetRAHEEN BUSINESS PARK
Manufacturer CityLIMERICK NA
Manufacturer Postal CodeNA
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameHYDROSET INJECTABLE CEMENT KIT 10CC
Generic NameIMPLANT
Product CodeGXP
Date Received2017-06-05
Catalog Number397010
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ORTHOPAEDICS-LIMERICK
Manufacturer AddressRAHEEN BUSINESS PARK LIMERICK NA NA


Patients

Patient NumberTreatmentOutcomeDate
10 2017-06-05

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