MAUDE Adverse Event Report: ARTHREX, INC. PERC INSERT KIT FOR 2.9MM P-LCK; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Model Number	PERC INSERT KIT FOR 2.9MM P-LCK
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	03/24/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The contribution of the device to the reported event could not be determined as the device was not returned for evaluation.The root cause of the event could not be determined from the information available and without device evaluation.If the device becomes available for evaluation, a follow-up report will be submitted.
Event or Problem Description
It was reported via a medwatch letter that a guidewire was missing from the tray, so a substitute wire was used from the ar-1923pk disposable instrument kit for tenodesis screw.The end of the wire broke off into patient, but was retrieved prior to closure of incision.

• Brand Name: PERC INSERT KIT FOR 2.9MM P-LCK
• Common Device Name: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
• Manufacturer (Section D): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• MDR Report Key: 11956478
• Report Number: 1220246-2021-03242
• Device Sequence Number: 4004306
• Product Code: LXH
• UDI-Device Identifier: 00888867096745
• UDI-Public: 00888867096745
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Nurse
• Type of Report: Initial
• Report Date (Section B): 06/08/2021

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: PERC INSERT KIT FOR 2.9MM P-LCK
• Device Catalogue Number: AR-1923PK
• Device Lot Number: 12123033
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/21/2021
• Initial Report FDA Received Date: 06/08/2021
• Patient Sequence Number: 1