5.0MM TI LOCKING SCREW W/T25 STARDRIVE 60MM FOR IM NAILS 04.005.550

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-31 for 5.0MM TI LOCKING SCREW W/T25 STARDRIVE 60MM FOR IM NAILS 04.005.550 manufactured by Oberdorf Synthes Produktions Gmbh.

Event Text Entries

[186117864] Event is reported as 2019, exact date of post-operative screw breakage is unknown. Complainant part is expected to be returned for manufacturer review/ investigation, but has yet to be received. Reporter is a synthes employee. (b)(4). Without a lot number the device history records review could not be completed. Product was not returned. Based on the information available, it has been determined that no corrective and/ or preventative action is proposed. This complaint will be accounted for and monitored via post market surveillance activities. If additional information is made available, the investigation will be updated as applicable. Device was used for treatment, not diagnosis. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


[186117865] Device report from synthes reports an event in (b)(6) as follows: it was reported that on (b)(6) 2019, the patient was implanted with retrograde/ antegrade femoral nail (rafn) 9mm x 400 mm, and 5. 0 mm locking screws (76mm x 1, 60mm x 1 and 32 mmx1). On (b)(6) 2019, the patient was readmitted due to the backed out 76mm screw. The 76mm screw was removed successfully. Post-op, when patient was doing physiotherapy and rehabilitation, patient started feeling pain again. Post-op x-ray was performed on an unknown date. The x-ray showed that the 60mm distal screw was broken, and this caused the nail to back out. The 60 mm screw remains in the patient. Patient has not returned for follow-up. Patient outcome is unknown. This report captures post-op breakage of 60mm distal screw while related complaint (b)(4) captures post-op event of backing out of 76mm screw. Concomitant devices reported: rafn nail (part number unknown, lot unknown, quantity 1), and 32 mm locking screw (part number unknown, lot unknown, quantity 1). This report involves one (1) 5. 0mm ti locking screw w/t25 stardrive 60mm for im nails. This is report 1 of 1 for (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8030965-2020-02426
MDR Report Key9903704
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-31
Date of Report2020-03-04
Date of Event2019-01-01
Date Mfgr Received2020-03-04
Date Added to Maude2020-03-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKARA DITTY-BOVARD
Manufacturer Street1302 WRIGHTS LANE EAST
Manufacturer CityWEST CHESTER PA 19380
Manufacturer CountryUS
Manufacturer Postal19380
Manufacturer Phone6103142063
Manufacturer G1WERK H
Manufacturer StreetIM BIFANG 6
Manufacturer CityHAEGENDORF 4614
Manufacturer CountrySZ
Manufacturer Postal Code4614
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name5.0MM TI LOCKING SCREW W/T25 STARDRIVE 60MM FOR IM NAILS
Generic NameSCREW,FIXATION,BONE
Product CodeHWC
Date Received2020-03-31
Catalog Number04.005.550
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerOBERDORF SYNTHES PRODUKTIONS GMBH
Manufacturer AddressEIMATTSTRASSE 3 OBERDORF 4436 SZ 4436


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-31

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