MAUDE Adverse Event Report: STRYKER ENDOSCOPY-SAN JOSE PKG 1688 AIM 4K CAMERA HEAD C-MOUNT; LAPAROSCOPE, GENERAL & PLASTIC SURGERY

Catalog Number	1688210105
Medical Device Problem Code	No Display/Image (1183)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	09/18/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Additional information will be provided once the investigation has been completed.
Event or Problem Description
It was reported that when preparing devices for use, camera and console, there was no picture.Sales representative has been contacted by the phone and decided to inspect the devices in person.After many tries it was not possible to get a picture.It was decided to send products to technical service.
Additional Manufacturer Narrative
The device was received at the local service facility for investigation.The technical service report indicates: i would like to inform you that the repair is complete.Replaced socket assembly (b)(4) and fiber optic connector (b)(4) in the camera console.Head and lens in working order.Equipment sent back to the customer.Probable root cause: cables.Hdmi cables.Connectors.Digital board.Power supply.Filter / fuse.Ac inlet board.Main board.Transition board.Intermittence between transition board and ch connector.Software.Camera head (sensor, sensor cable).Coupler (dust on optics, scratched optics, broken / shifted lenses, focusing mechanism, endoclamp, zoom ring).Problem toggling light source.Connected monitors.Leaking.Poor grounding (e.G camera head connection from cable to transition board.) no/incorrect communication with light source.Soaking cap disconnection during sterilization.Electromagnetic interference (emi) from rf communication, hf surgical instruments, esd, or power surge.Cybersecurity attack.Pendulum ch inertial measurement unit (imu).Use error.The reported failure mode will be monitored for future reoccurrence.
Event or Problem Description
It was reported that when preparing devices for use, camera and console, there was no picture.Sales rep has been contacted by the phone and decided to inspect the devices in person.After many tries it was not possible to get a picture.It was decided to send products to technical service.

• Brand Name: PKG 1688 AIM 4K CAMERA HEAD C-MOUNT
• Common Device Name: LAPAROSCOPE, GENERAL & PLASTIC SURGERY
• 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: 23318041
• Report Number: 0002936485-2025-00849
• Device Sequence Number: 4838541
• Product Code: GCJ
• UDI-Device Identifier: 07613327418989
• UDI-Public: 07613327418989
• Combination Product (Y/N): N
• Initial Reporter Country: PL
• PMA/510(K) Number: K182160
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Nurse
• Type of Report: Initial,Followup
• Report Date (Section B): 12/11/2025

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 Catalogue Number: 1688210105
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 09/18/2025
• Supplement Date Received by Manufacturer: 12/02/2025
• Initial Report FDA Received Date: 10/16/2025
• Supplement Report FDA Received Date: 12/11/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/01/2023
• 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
• Patient Sex: Unknown