MAUDE Adverse Event Report: Stryker Endoscopy-San Jose PKG L10 LED LIGHT SOURCE WITH AIM; Confocal optical imaging

Catalog Number	0220220300
Medical Device Problem Codes	Overheating of Device (1437); Device Sensing Problem (2917)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/13/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that test all items (l10 light source (ref 220-220-300/sn (b)(6)), safelight light cable, and safelight adapter) connected to the event immediately upon availability of the room, confirming that the action continues to occur on this device only.The light cable and adapter functioned as intended with a separate device.Additionally, we tested a separate light cable and adapter with the device in question, which again resulted in a failed triggering of the safelight safety function.This only happened in one procedure.Not aware about issue with the device.
Additional Manufacturer Narrative
Additional information will be provided once the investigation has been completed.

• Brand Name: PKG L10 LED LIGHT SOURCE WITH AIM
• Common Device Name: Confocal optical imaging
• 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 ; +1(408)754-2000
• MDR Report Key: 25487289
• Report Number: 0002936485-2026-00379
• Device Sequence Number: 9930510
• Product Code: OWN
• UDI-Device Identifier: 07613327051377
• UDI-Public: (01)07613327051377
• Combination Product (Y/N): N
• Initial Reporter State: WI
• Initial Reporter Country: US
• PMA/510(K) Number: K142310
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial,Followup
• Report Date (Section B): 09/16/2026

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: 0220220300
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 05/22/2026
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 05/13/2026
• Supplement Date Received by Manufacturer: 08/20/2026
• Initial Report FDA Received Date: 06/12/2026
• Supplement Report FDA Received Date: 09/16/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/01/2017
• 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