MAUDE Adverse Event Report: STRYKER ENDOSCOPY-SAN JOSE SINGLE FIBER OPTIC CABLE, PINK, 10 FT, ACMI; LIGHT, SURGICAL, FIBEROPTIC

Catalog Number	FC1SP
Medical Device Problem Codes	Overheating of Device (1437); Temperature Problem (3022)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/29/2025
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 that the light cord was plugged into a stryker l11 light source and became very hot after only 30 minutes of being plugged in.
Additional Manufacturer Narrative
Three attempts have been made to retrieve the device for evaluation, and it is yet to be received in-house.No further attempts to retrieve the device are required.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: cord very hot probable root cause: -inadequate material selection of cable -use error of resting unconnected cable on drape -use error of connecting inappropriate light source or using inappropriate light source settings -use error of using damaged device the reported failure mode will be monitored for future reoccurrence.
Event or Problem Description
It was reported that the light cord was plugged into a stryker l11 light source and became very hot after only 30 minutes of being plugged in.

• Brand Name: SINGLE FIBER OPTIC CABLE, PINK, 10 FT, ACMI
• Common Device Name: LIGHT, SURGICAL, FIBEROPTIC
• 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: 22091106
• Report Number: 0002936485-2025-00473
• Device Sequence Number: 20566815
• Product Code: FST
• UDI-Device Identifier: 00816728020202
• UDI-Public: 00816728020202
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K090070
• 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): 08/11/2025

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: FC1SP
• Device Lot Number: 173135
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 04/29/2025
• Supplement Date Received by Manufacturer: 07/15/2025
• Initial Report FDA Received Date: 05/27/2025
• Supplement Report FDA Received Date: 08/11/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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