MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC CANNULATED 4.0MM HEXAGONAL SCREWDRIVER; SCREWDRIVERS

Model Number	313.93
Medical Device Problem Code	Contamination /Decontamination Problem (2895)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).Complainant device is expected to be returned for manufacturer review/investigation.The investigation could not be completed, no product was received; no conclusion could be drawn at the time of filing this report.The investigation could not be completed, no product was received; no conclusion could be drawn at the time of filing this report.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 europe reports an event in (b)(6) as follows: it was reported that during field inspection and sterile processing, all the simili wood handle of the screwdriver are leaving residue in the peel pack.A brown spot making the responsible this complaint involves five (5) devices.This report is for one (1) cannulated 4.0mm hexagonal screwdriver.This report is 3 of 5 for (b)(4).
Additional Manufacturer Narrative
Product complaint # (b)(4).Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.D9: product received.H3, h6: investigation summary: investigation flow: visual.Visual inspection: the solid hexagonal screw driver (part# 313.930, lot # 8368907, quantity # (b)(4)) was received at us cq.Upon visual inspection at cq, it was noticed that there were minor scratches on the surface of the shaft and the handle was discolored but there is no evidence of foreign substance on the surface of the device.Defect identified/ device failure was not confirmed.Complaint was not confirmed.Investigation conclusion: the complaint condition was not confirmed for the solid hexagonal screw driver (part# 313.930, lot # 8368907, quantity # (b)(4)) as the device received was decontaminated and no residue was observed on the device.There is no indication that a design or manufacturing issue has caused the complaint condition and hence the root cause cannot be determined.Based on the investigation findings, it has been determined that no corrective and/or preventative action is proposed.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post market safety surveillance activities.Device history lot: part # 313.930; lot # 8368907; release to warehouse date: mar 28, 2013.Manufacturer: hagendorf.No ncr's were generated during production.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.

• Brand Name: CANNULATED 4.0MM HEXAGONAL SCREWDRIVER
• Common Device Name: SCREWDRIVERS
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• MDR Report Key: 12084053
• Report Number: 2939274-2021-03289
• Device Sequence Number: 3235941
• Product Code: HXX
• UDI-Device Identifier: 10886982188243
• UDI-Public: 10886982188243
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 06/05/2021

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 Model Number: 313.93
• Device Catalogue Number: 313.930-US
• Device Lot Number: 8368907
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/15/2021
• Initial Date Received by Manufacturer: 06/05/2021
• Supplement Date Received by Manufacturer: 07/28/2021
• Initial Report FDA Received Date: 06/29/2021
• Supplement Report FDA Received Date: 08/12/2021
• 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: SCRDRIVER T25 SELF-HOLDING L290; SCRDRIVER-HEX Ø3.5 COMBINED W/STARDR T25; SCRDRIVER-HEX-SMALL W/HOLD-SLEEVE; SCRDRIVERSHAFT-HEX F/CANNSCR Ø6.5+7.3; SCRDRIVER T25 SELF-HOLDING L290.; SCRDRIVER-HEX Ø3.5 COMBINED W/STARDR T25.; SCRDRIVER-HEX-SMALL W/HOLD-SLEEVE.; SCRDRIVERSHAFT-HEX F/CANNSCR Ø6.5+7.3.