MAUDE Adverse Event Report: STRYKER ENDOSCOPY-SAN JOSE HD 4MMX70° LG ARTHROSCOPE SPEEDLOCK A/C

Catalog Number	0502204070
Medical Device Problem Code	Poor Quality Image (1408)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/02/2025
Type of Reportable Event	Malfunction
Additional 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 or Problem Description
It was reported the device was blurry during procedure.The surgeon had to end the surgery early and wake up the patient.Anesthesia was introduced and an incision was made prior to cancellation.
Event or Problem Description
It was reported the device was blurry during procedure.The surgeon had to end the surgery early and wake up the patient.Anesthesia was introduced and an incision was made prior to cancellation.
Additional Manufacturer Narrative
Alleged failure: "yesterday during a hip scope - our loan 70 degree arthroscope was broken.The image was blurry and when a different scope was attached it worked fine.This was the only sterilised 70 degree on site - the surgeon had to end the surgery early and wake up the patient." anesthesia was introduced and an incision was made prior to cancellation.The failure(s) identified in the investigation is consistent with the complaint record.The probable root cause could be a cracked lens.The product was returned for investigation and the failure mode will be monitored for future reoccurrence.

• Brand Name: HD 4MMX70° LG ARTHROSCOPE SPEEDLOCK A/C
• Common Device Name: ARTHROSCOPE
• 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: arsalan rizvi ; 5900 optical court; san jose, CA 95138 ; 4087542000
• MDR Report Key: 23382264
• Report Number: 0002936485-2025-00893
• Device Sequence Number: 8645108
• Product Code: HRX
• UDI-Device Identifier: 07613327053630
• UDI-Public: 07613327053630
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: K962075
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 12/30/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: 0502204070
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 10/03/2025
• Supplement Date Received by Manufacturer: 12/16/2025
• Initial Report FDA Received Date: 10/24/2025
• Supplement Report FDA Received Date: 12/30/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown