MAUDE Adverse Event Report: Arthrex, Inc. NanoScopic Release System; LAPAROSCOPE

Model Number	NanoScopic Release System
Medical Device Problem Code	No Display/Image (1183)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	08/26/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
On 27 august 2026, it was reported by a sales representative via email that an ar-8850ds, nanoscopic release system was reported to have nanoscope faulty.No images can be seen.Surgeon can't see a thing.This occurred on (b)(6) 2026 during a endoscopic carpal tunnel release procedure.The case was completed successfully.Procedure had to be done open.There was case involvement.
Additional Manufacturer Narrative
Investigation is in process.A follow-up report will be provided upon availability of additional information.

• Brand Name: NanoScopic Release System
• Common Device Name: LAPAROSCOPE
• Manufacturer (Section D): Arthrex, Inc.; 1370 creekside boulevard; naples FL 34108 -194
• Manufacturer (Section G): Arthrex, Inc.; 1370 creekside boulevard; naples FL 34108 -194
• Manufacturer Contact: jared engle ; +1(800)933-7001
• MDR Report Key: 50733284
• Report Number: 1220246-2026-04687
• Device Sequence Number: 21479435
• Product Code: GCJ
• UDI-Device Identifier: 00888867390300
• UDI-Public: (01)00888867390300(11)251201(17)301130(10)6076177999
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K243008
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Distributor
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial
• Report Date (Section B): 09/11/2026

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?: No
• Operator of Device: Health Professional
• Device Model Number: NanoScopic Release System
• Device Catalogue Number: AR-8850DS
• Device Lot Number: 6076177999
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/26/2026
• Initial Report FDA Received Date: 09/11/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 12/01/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown