MAUDE Adverse Event Report: ARTHREX, INC. TORPEDO, 5.0MM X 13 CM; BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

Model Number	TORPEDO, 5.0MM X 13 CM
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	06/30/2021
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
On (b)(6) 2021, it was reported by a¿sales representative¿via¿sems¿that 2 of the ar-8500td¿torpedo, 5.0mm x 13 cm metal tips broke off during the procedure.This was¿discovered during¿a shoulder procedure.¿how the procedure was completed if occurred during use.¿a 3rd ar-8500td shaver was opened to compare, making sure all pieces were found.A portable x-ray was done while the patient was still in the or, no foreign objects were seen on x-ray.Additional information 8/3/2021 the sales rep reported the incident occurred during one of the dr's.Shoulder scopes.Two torpedo shavers were broken during a normal bursectomy in the sub-acromial space.

• Brand Name: TORPEDO, 5.0MM X 13 CM
• Common Device Name: BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL
• Manufacturer (Section D): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• MDR Report Key: 12333389
• Report Number: 1220246-2021-03525
• Device Sequence Number: 3935837
• Product Code: GFA
• UDI-Device Identifier: 00888867043923
• UDI-Public: 00888867043923
• Combination Product (Y/N): N
• Initial Reporter State: WI
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: distributor
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial
• Report Date (Section B): 08/17/2021

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 Expiration Date: 12/31/2025
• Device Model Number: TORPEDO, 5.0MM X 13 CM
• Device Catalogue Number: AR-8500TD
• Device Lot Number: 12612482
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/27/2021
• Initial Report FDA Received Date: 08/17/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1