MAUDE Adverse Event Report: SMITH & NEPHEW, INC. ELECTROBLADE RESECTOR,4.5 FULL RADIUS; ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Catalog Number	7209855
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	12/27/2018
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that during the surgery it was noticed metal shavings in the tissue and the device locked up.The procedure was successfully completed with and unknown delay using a back up device.No patient injury or other complications were reported.
Additional Manufacturer Narrative
H10: h6: visual inspection and functional testing could not be performed because the device in question has not been returned for evaluation.Thus, the complaint could not be verified and a root cause could not be determined with confidence.It is difficult to perform an accurate evaluation of a failure without having the failed product to look at.As such the complaint is being closed without conclusion.However, if the product is returned in the future the complaint can be reopened and evaluated.

• Brand Name: ELECTROBLADE RESECTOR,4.5 FULL RADIUS
• Common Device Name: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 150 minuteman road; andover MA 01810
• MDR Report Key: 8356336
• Report Number: 3003604053-2019-00016
• Device Sequence Number: 1959976
• Product Code: GEI
• UDI-Device Identifier: 03596010492302
• UDI-Public: 03596010492302
• Combination Product (Y/N): N
• Initial Reporter State: KY
• Initial Reporter Country: US
• PMA/510(K) Number: K012314
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/15/2019

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: 10/31/2021
• Device Catalogue Number: 7209855
• Device Lot Number: 4476052
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 01/28/2019
• Supplement Date Received by Manufacturer: 04/12/2019
• Initial Report FDA Received Date: 02/20/2019
• Supplement Report FDA Received Date: 04/15/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1