MAUDE Adverse Event Report: STRYKER ENDOSCOPY-SAN JOSE PKG, RESECTOSCOPE CABLE, (VALLEYLAB/BOVIE); CYSTOSCOPE AND ACCESSORIES, FLEXIBLE/RIGID

Model Number 0502990300

Device Problems Sparking (2595); Electrical Shorting (2926)

Patient Problems Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)

Event Date 01/01/2020

Event Type  malfunction  

Manufacturer Narrative

Additional information will be provided once the investigation has been completed.The device manufacturer date is not known at this time.However, should it become available it will be provided in future reports.

Event Description

It was reported that the device sparked.

Event Description

It was reported that the device sparked.

Manufacturer Narrative

The device manufacture date is not known.This complaint investigation was closed based on the device not received, therefore the reported failure mode was not confirmed.In the event that the device is received, the complaint will be reopened and the investigation will be updated with new results.Alleged failure: sparked and broke during procedure.Probable root cause: generator power malfunction; material/design error; conductive irrigant used; improper use with another electromedical device; use error.The reported failure mode will be monitored for future reoccurrence.H3 other text: 81.

• Brand Name: PKG, RESECTOSCOPE CABLE, (VALLEYLAB/BOVIE)
• Type of Device: CYSTOSCOPE AND ACCESSORIES, FLEXIBLE/RIGID
• Manufacturer (Section D): STRYKER ENDOSCOPY-SAN JOSE; 5900 optical court; san jose CA 95138
• Manufacturer (Section G): STRYKER ENDOSCOPY-SAN JOSE; 5900 optical court; san jose CA 95138
• Manufacturer Contact: chester rebugio ; 5900 optical court; san jose, CA 95138 ; 4087542000
• MDR Report Key: 15501896
• MDR Text Key: 306262749
• Report Number: 0002936485-2022-00534
• Device Sequence Number: 1
• Product Code: FAJ
• UDI-Device Identifier: 07613327064018
• UDI-Public: 07613327064018
• Combination Product (y/n): N
• Reporter Country Code: CA
• PMA/PMN Number: K040390
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 12/06/2022

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
• Device Operator: Health Professional
• Device Model Number: 0502990300
• Device Catalogue Number: 0502990300
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 09/06/2022
• Initial Date FDA Received: 09/29/2022
• Supplement Dates Manufacturer Received: 09/06/2022
• Supplement Dates FDA Received: 12/06/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1