MAUDE Adverse Event Report: OBERDORF SYNTHES PRODUKTIONS GMBH CONICAL EXTRACTION SCREW FOR 3.5MM SCREWS; EXTRACTOR

Catalog Number	309.521
Medical Device Problem Code	Material Twisted/Bent (2981)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Initial reporter is synthes sales representative.Device history records review was completed for part: 309.521, lot: 9588804.Manufacturing location: bettlach, release to warehouse date: nov 12, 2015.A manufacturing record evaluation was performed for the finished device lot number, and no non-conformance were identified.Product investigation was completed.Upon visual inspection, the distal tip of the device had stripped threads.There remaining of the device showed surface wear consistent with use which would not impact the functionality of the device.Because of the damages, the complaint relevant dimensions cannot be checked to print specifications anymore.The manufacturing review shows that the production procedure was according to the specifications and there were no issues that would contribute to this complaint condition.Due to the stripped thread, the complaint condition is rated as confirmed.Because of the damage, it is not possible to measure the relevant dimension.The damage is clearly caused post manufacturing.Due to the damage signs we can assume that this product was an often and intensive used instrument.The damage at the tip indicates that a mechanical overloading situation during its use could likely caused the deformation of the tip.As per the leaflet ¿important information¿: end of life of a device is normally determined by wear and damage due to use.Evidence of damage and wear on a device may include but is not limited to corrosion (i.E.Rust, pitting), discoloration, excessive scratches, flaking, wear and cracks.Improperly functioning devices, devices with unrecognizable markings, missing or removed (buffed off) part numbers, damaged and excessively worn devices should not be used.Based on the investigation findings, it has been determined that no corrective and/or preventative action is proposed as no product related issue could be detected.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 (b)(6) reports an event as follows: it was reported that on an unknown date, a patient underwent an osteosynthesis surgery with the proximal humerus internal locking system (philos) due to a fracture.During the implantation of the proximal humeral plate, it was impossible to remove the plate from the insertion handle.The surgeon removed the implanted plate due to it was impossible to detach the insertion handle and another plate was implanted but not mini-invasive.There was a surgical delay of at least 2 hours.Procedure and patient outcome are unknown.Due to system limitation, this event is captured under this (b)(4) and linked (b)(4).Concomitant device: screw (part unknown, lot unknown, quantity unknown).This report is for one (1) extraction screw.This is report 10 of 10 for (b)(4).

• Brand Name: CONICAL EXTRACTION SCREW FOR 3.5MM SCREWS
• Common Device Name: EXTRACTOR
• Manufacturer (Section D): OBERDORF SYNTHES PRODUKTIONS GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• MDR Report Key: 8650106
• Report Number: 8030965-2019-64633
• Device Sequence Number: 11572363
• Product Code: HWB
• UDI-Device Identifier: 07611819204409
• UDI-Public: (01)07611819204409
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• 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: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 04/02/2019

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: 309.521
• Device Lot Number: 9588804
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/24/2019
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/30/2019
• Initial Report FDA Received Date: 05/29/2019
• 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: UNK - SCREWS: TRAUMA