MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC 6.5MM CANCELLOUS BONE SCREW 16MM THREAD/85MM; SCREW, FIXATION, BONE

Model Number	216.085
Medical Device Problem Code	Material Twisted/Bent (2981)
Health Effect - Clinical Code	No Patient Involvement (2645)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Additional device product code: ktt.Complainant part is expected to be returned for manufacturer review/investigation, but has yet to be received.Reporter is synthes sales consultant.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
It was reported on (b)(6) 2018, during sterile processing, it was found out that the two (2) hexagon screw recessed of the partially threaded had a metal shaving that was broke loose and one (1) hexagon screw had a metal shaving that was still stuck in the hexagon screw.There was no patient involvement.This report is for one (1) 6.5mm cancellous bone screw 16mm thread/85mm.This is report 3 of 3 for complaint (b)(4).
Additional Manufacturer Narrative
It was reported on (b)(6) 2018, during sterile processing, it was found out that the two (2) hexagon screw recessed of the partially threaded with a metal shavings that was broke loose and one (1) hexagon screw had a metal shaving that was still stuck in the hexagon screw.There was no patient involvement.Flow: damage: visual (appearance not as expected).Visual inspection performed at customer quality (cq) no issues were noted with the implant, there is no evidence that threads peeled/broken.On the screw head there is a piece of metal shaving embedded inside however the shaving does not appear to be part of any of the screws that were returned.There were metal shavings that came back; however they don't belong to any of the returned implants.The received condition does not agree with the complaint description and is unconfirmed.While no definitive root cause could be determined as no issues with the implant itself were discovered.During the investigation, no product design or manufacturing issues were observed that may have contributed to the complaint condition.Based on the investigation findings, it has been determined that no corrective and/or preventative action is proposed.Device was used for treatment, not diagnosis.
Additional Manufacturer Narrative
The device was received, and the product evaluation is in progress.No conclusion can be drawn.Additionally, device history records review could not be completed without lot number.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: 6.5MM CANCELLOUS BONE SCREW 16MM THREAD/85MM
• Common Device Name: SCREW, FIXATION, BONE
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• MDR Report Key: 8034071
• Report Number: 2939274-2018-54752
• Device Sequence Number: 13827550
• Product Code: HWC
• UDI-Device Identifier: 10886982155283
• UDI-Public: (01)10886982155283
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K061621
• 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,Followup
• Report Date (Section B): 10/17/2018

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: 216.085
• Device Catalogue Number: 216.085
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/07/2018
• Initial Date Received by Manufacturer: 10/17/2018
• Supplement Date Received by Manufacturer: 11/07/2018; 12/10/2018
• Initial Report FDA Received Date: 11/02/2018
• Supplement Report FDA Received Date: 11/19/2018; 12/11/2018
• Patient Sequence Number: 1