MAUDE Adverse Event Report: ZIMMER SPINE FINAL SCREWDRIVER SHAFT; INSTINCT JAVA SYSTEM

Catalog Number	046W1AN00640
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/14/2022
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Without a product return, no product evaluation is able to be conducted.Current information is insufficient to permit a valid conclusion about the cause of this event.If additional information is obtained that adds value to the relevant content of this report and/or a conclusion can be drawn, a follow-up report will be sent.Reference reports 3003853072-2022-00003 through 3003853072-2022-00005.
Event or Problem Description
It was reported that the tips of three instinct java screwdrivers broke on three different closure tops during final tightening intra-operatively.One of the broken tips of the screwdriver could not be removed from the closure top and remains implanted.The surgery was completed with another device.This is report three of three for this event.
Additional Manufacturer Narrative
Device evaluation: visual inspection revealed that the tips of each devices were twisted and fractured.One fractured off tip was returned.Potential cause: root cause was unable to be determined.This event could possibly be attributed to wear through use over time or multiple sterilization cycles.It could also be attributed to applying off-axis forces to the driver.Dhr review: per dhr review, the parts were likely conforming when they left zimvie control.Device use: this device is used for treatment.If additional information is obtained that adds value to the relevant content of this report, a follow-up report will be sent.
Event or Problem Description
It was reported that the tips of three instinct java screwdrivers broke on three different closure tops during final tightening intra-operatively.One of the broken tips of the screwdriver could not be removed from the closure top and remains implanted.The surgery was completed with another device.This is report three of three for this event.
Additional Manufacturer Narrative
Current information is insufficient to permit a valid conclusion about the cause of this event.A follow up report will be sent upon completion of the device evaluation.
Event or Problem Description
It was reported that the tips of three instinct java screwdrivers broke on three different closure tops during final tightening intra-operatively.One of the broken tips of the screwdriver could not be removed from the closure top and remains implanted.The surgery was completed with another device.This is report three of three for this event.

• Brand Name: FINAL SCREWDRIVER SHAFT
• Common Device Name: INSTINCT JAVA SYSTEM
• Manufacturer (Section D): ZIMMER SPINE; 23 parvis des chartrons; cite mondiale; bordeaux, cedex 33080 ; FR 33080
• Manufacturer (Section G): ZIMMER SPINE; 23 parvis des chartrons; cite mondiale; bordeaux, cedex 33080 ; FR 33080
• Manufacturer Contact: kim martinez ; 10225 westmoor dr.; na; westminster, CO 80021 ; 3035144809
• MDR Report Key: 14407733
• Report Number: 3003853072-2022-00005
• Device Sequence Number: 5564341
• Product Code: NKB
• UDI-Device Identifier: 00889024342187
• UDI-Public: (01)00889024342187(10)A2418908A(11)160923
• Combination Product (Y/N): N
• Initial Reporter Country: IN
• PMA/510(K) Number: K111301
• 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,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 08/31/2022

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: 046W1AN00640
• Device Lot Number: A2418908A
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/18/2022
• Supplement Date Received by Manufacturer: 06/21/2022; 08/19/2022
• Initial Report FDA Received Date: 05/16/2022
• Supplement Report FDA Received Date: 07/14/2022; 08/31/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 09/23/2016
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown