MAUDE Adverse Event Report: SYNTHES GMBH 4.0MM CANCELLOUS BONE SCREW FULLY THREADED/18MM; SCREW, FIXATION, BONE

Model Number	206.018
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Hypersensitivity/Allergic reaction (1907)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
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.Common device name: additional procode: hrs.Device available for evaluation: complainant part is not expected to be returned for manufacturer review/investigation.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 denmark reports an event as follows: it was reported that on an unknown date, a patient experienced an allergic reaction caused by an implant in the ankle.No further information was provided.This report is for a 4.0mm cancellous bone screw fully threaded/18mm.This is report 7 of 10 for (b)(4).
Event or Problem Description
This is report 8 of 10 for (b)(4).
Additional Manufacturer Narrative
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.Product was not returned.Based on the information available, it has been determined that no corrective and 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.

• Brand Name: 4.0MM CANCELLOUS BONE SCREW FULLY THREADED/18MM
• Common Device Name: SCREW, FIXATION, BONE
• Manufacturer (Section D): SYNTHES GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• Manufacturer (Section G): SYNTHES SELZACH; bohackerweg 5; selzach 2545 ; SZ 2545
• Manufacturer Contact: kate karberg ; 1302 wright lane east; west chester, PA ; 3035526892
• MDR Report Key: 15914031
• Report Number: 8030965-2022-10564
• Device Sequence Number: 4347492
• Product Code: HWC
• UDI-Device Identifier: 10886982147240
• UDI-Public: (01)10886982147240
• Combination Product (Y/N): N
• Initial Reporter Country: DA
• PMA/510(K) Number: K083213
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 12/02/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 206.018
• Device Catalogue Number: 206.018
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 11/10/2022
• Supplement Date Received by Manufacturer: 12/15/2022
• Initial Report FDA Received Date: 12/05/2022
• Supplement Report FDA Received Date: 01/09/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: CANCELLOUSSCR Ø4 FULL-THR L18 SST; CANCELLOUSSCR Ø4 FULL-THR L18 SST; CORTSCR Ø3.5 SELF-TAP L14 SST; CORTSCR Ø3.5 SELF-TAP L14 SST; CORTSCR Ø3.5 SELF-TAP L16 SST; CORTSCR Ø3.5 SELF-TAP L24 SST; CORTSCR Ø3.5 SELF-TAP L50 SST; CORTSCR Ø3.5 SELF-TAP L50 SST; LCP 1/3-TUB-PL 3.5 7HO L88 SST
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown