MAUDE Adverse Event Report: OBERDORF SYNTHES PRODUKTIONS GMBH STARDRIVE SCREWDRIVER T25/SELF-RETAINING/LONG

Catalog Number	03.010.108
Medical Device Problem Code	Material Twisted/Bent (2981)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	09/25/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Complainant part is expected to be returned for manufacturer review/investigation, but has yet to be received.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.
Event or Problem Description
Device report from synthes reports an event in (b)(6) as follows: it was reported during a procedure on (b)(6) 2020 several issues occurred intraoperatively which included device malfunctions and missing implant components.The surgeon noted the main implants were missing associated locking screws.Some of the screw lengths were on back order however, there were other lengths of screws in the set additionally, the long t25 screwdriver was worn and would not engage the recess of the screws well.The connecting screw for the nail was worn out and did not connect to the implant properly.Also, during the surgery, the surgeon used the aiming guide to drill for the proximal screws.Once the screws were implanted, an x-ray was taken and it was noted that the screws missed the nail.The surgery was delayed 60 minutes and the procedure was completed using a competitor's nail.This is report 2 of 7 (b)(4).

• Brand Name: STARDRIVE SCREWDRIVER T25/SELF-RETAINING/LONG
• Common Device Name: SCREWDRIVER
• Manufacturer (Section D): OBERDORF SYNTHES PRODUKTIONS GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• MDR Report Key: 10684333
• Report Number: 8030965-2020-07946
• Device Sequence Number: 3208869
• Product Code: HXX
• UDI-Device Identifier: 07611819765733
• UDI-Public: (01)07611819765733
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 09/25/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: 03.010.108
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 09/25/2020
• Initial Report FDA Received Date: 10/15/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: AIM-ARM F/EXPERT ALFN; CONNECSCR CANN F/EXPERT TN+FN F/03.010.0; HIP SCR Ø5 SELF-TAP L55 F/EXPERT ALFN TA; LOCKSCR Ø4 L66 F/NAILS TAN DBLUE; UNK - NAILS; UNK - SCREWS: TRAUMA