MAUDE Adverse Event Report: COSMAN MEDICAL CSK-TC ELECTRODE; ELECTRODES

Model Number	CSK-TC15-3M
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	10/18/2017
Type of Reportable Event	Malfunction
Event or Problem Description
The returned electrode was analyzed and confirmed the electrode shaft was broken off at the hub, due to external mechanical force.
Additional Manufacturer Narrative
Additional information was received that the electrode was physically broken prior to return for analysis.No additional information can be obtained.
Event or Problem Description
The returned electrode was analyzed and confirmed the electrode shaft was broken off at the hub, due to external mechanical force.

• Brand Name: CSK-TC ELECTRODE
• Common Device Name: ELECTRODES
• Manufacturer (Section D): COSMAN MEDICAL; 22 terry ave; burlington MA 01803
• MDR Report Key: 6960020
• Report Number: 3006630150-2017-04090
• Device Sequence Number: 19031507
• Product Code: GXI
• UDI-Device Identifier: 00813250011548
• UDI-Public: 00813250011548
• Combination Product (Y/N): N
• Initial Reporter State: GA
• Initial Reporter Country: US
• PMA/510(K) Number: K050084
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 10/18/2017

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: Physician
• Device Model Number: CSK-TC15-3M
• Device Lot Number: L481
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 09/25/2017
• Initial Date Received by Manufacturer: 10/18/2017
• Supplement Date Received by Manufacturer: 10/31/2017
• Initial Report FDA Received Date: 10/18/2017
• Supplement Report FDA Received Date: 11/07/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1