UN3 SCREWS, SELF-DRILLING, 1.5X4MM, 5/P 56-15904

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-16 for UN3 SCREWS, SELF-DRILLING, 1.5X4MM, 5/P 56-15904 manufactured by Stryker Leibinger Freiburg.

Event Text Entries

[145367717] Device is not available for evaluation. If additional information is received it will be reported on a supplemental report. Distributor cannot return for evaluation.
Patient Sequence No: 1, Text Type: N, H10


[145367718] It was reported by the distributor that there was an issue during a hydrocephalus case. While the surgeon was implanting a screw he could not properly drive screw into the skull as it kept slipping. There was no significant delay or patient harm reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008010177-2019-00016
MDR Report Key8617849
Date Received2019-05-16
Date of Report2019-05-16
Date of Event2019-03-09
Date Mfgr Received2019-05-10
Date Added to Maude2019-05-16
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. RYLEE KOOLE
Manufacturer StreetBOETZINGERSTR. 41
Manufacturer CityFREIBURG D-79111
Manufacturer PostalD-79111
Manufacturer Phone76145120
Manufacturer G1STRYKER LEIBINGER FREIBURG
Manufacturer StreetBOETZINGERSTR. 41
Manufacturer CityFREIBURG D-79111
Manufacturer Postal CodeD-79111
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameUN3 SCREWS, SELF-DRILLING, 1.5X4MM, 5/P
Generic NameIMPLANT
Product CodeHBW
Date Received2019-05-16
Catalog Number56-15904
Lot Number1000297572
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER LEIBINGER FREIBURG
Manufacturer AddressBOETZINGERSTR. 41 FREIBURG D-79111 D-79111


Patients

Patient NumberTreatmentOutcomeDate
10 2019-05-16

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