MAUDE Adverse Event Report: K2M, INC. MI OFFSET ROD REDUCER; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Model Number	5101-90012
Medical Device Problem Codes	Material Deformation (2976); Failure to Eject (4010)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/11/2022
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the everest mi offset rod reducer was difficult to come off of the screw and was broken/bent when attempting to remove.The surgery was completed successfully with no surgical delay.No adverse consequences or medical intervention were reported.
Additional Manufacturer Narrative
H6 coding has been updated to reflect investigation conclusion.H3 other text: no product returned.
Event or Problem Description
It was reported that the everest mi offset rod reducer was difficult to come off of the screw and was broken/bent when attempting to remove.The surgery was completed successfully with no surgical delay.No adverse consequences or medical intervention were reported.

• Brand Name: MI OFFSET ROD REDUCER
• Common Device Name: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
• Manufacturer (Section D): K2M, INC.; 600 hope parkway se; leesburg VA 20175
• Manufacturer (Section G): K2M, INC.; 600 hope parkway se; leesburg VA 20175
• Manufacturer Contact: rita karan ; 2 pearl court; allendale, NJ 07401 ; 2017608000
• MDR Report Key: 15185999
• Report Number: 3004774118-2022-00319
• Device Sequence Number: 6390467
• Product Code: LXH
• UDI-Device Identifier: 10888857104006
• UDI-Public: 10888857104006
• Combination Product (Y/N): N
• Initial Reporter State: VA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 11/04/2022

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 Model Number: 5101-90012
• Device Catalogue Number: 5101-90012
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 07/11/2022
• Supplement Date Received by Manufacturer: 10/07/2022
• Initial Report FDA Received Date: 08/08/2022
• Supplement Report FDA Received Date: 11/04/2022
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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