MAUDE Adverse Event Report: SYNTHES GMBH 2.7MM TI VA LCP CLAVICLE PLATE LATERAL/ CS1/ LEFT/ STERILE; PLATE, FIXATION, BONE

Catalog Number 04.112.610S

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Joint Dislocation (2374)

Event Date 01/01/2021

Event Type  Injury  

Manufacturer Narrative

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 Description

Device report from synthes reports an event in (b)(6) as follows: it was reported that on an unknown date a patient had a 2.7 variable angle (va) clavicle plate lat cs1 implanted to treat lateral clavicle fracture.Post-operatively patient had a acromioclavicular joint dislocation requiring revision surgery.No further information provided.This report is for one (1) 2.7mm ti va lcp clavicle plate lateral/ cs1/ left/ sterile.This is report 1 of 2 for complaint (b)(4).

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.H10 additional narrative: a2: date of birth is an unknown date in 1997.B3: date of event is an unknown date in 2021.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 Description

It was further reported that the device had been implanted for one month and nineteen days at the time of discovery of the complaint.

• Brand Name: 2.7MM TI VA LCP CLAVICLE PLATE LATERAL/ CS1/ LEFT/ STERILE
• Type of Device: PLATE, FIXATION, BONE
• Manufacturer (Section D): SYNTHES GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• MDR Report Key: 12377447
• MDR Text Key: 268468947
• Report Number: 8030965-2021-07269
• Device Sequence Number: 1
• Product Code: HRS
• UDI-Device Identifier: 07612334214287
• UDI-Public: (01)07612334214287
• Combination Product (y/n): N
• PMA/PMN Number: K203414
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Type of Report: Initial,Followup
• Report Date: 08/18/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/27/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: 04.112.610S
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 09/24/2021
• Patient Sequence Number: 1
• Treatment: UNK - SCREWS: CORTEX; UNK - SCREWS: CORTEX; UNK - SCREWS: CORTEX
• Patient Outcome(s): Required Intervention
• Patient Age: 24 YR