MAUDE Adverse Event Report: COSMAN MEDICAL CSK 10CM TC ELECTRODE WITH 3M CABLE; ELECTRODES

Model Number	CSK-TC10-3M
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	08/01/2018
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Field expiration date: na field occupation: medical professional.
Event or Problem Description
The visual inspection on the returned electrode revealed that electrode shaft was broken right at the hub.The functional test could not be performed due to broken electrode.

• Brand Name: CSK 10CM TC ELECTRODE WITH 3M CABLE
• Common Device Name: ELECTRODES
• Manufacturer (Section D): COSMAN MEDICAL; 22 terry ave; burlington MA 01803
• MDR Report Key: 7739442
• Report Number: 3006630150-2018-02295
• Device Sequence Number: 11022999
• Product Code: GXI
• UDI-Device Identifier: 00813250011524
• UDI-Public: 00813250011524
• Combination Product (Y/N): N
• Initial Reporter State: FL
• 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
• Report Date (Section B): 08/01/2018

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: CSK-TC10-3M
• Device Lot Number: N195
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/30/2018
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/01/2018
• Initial Report FDA Received Date: 08/01/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1