MAUDE Adverse Event Report: Conmed Corporation ANCHOR TISSUE RETRIEVAL SYSTEM; Laparoscope, general plastic surgery

Model Number	TRS-ROBO-8
Medical Device Problem Code	Material Integrity Problem (2978)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/21/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The bag fell apart.

• Brand Name: ANCHOR TISSUE RETRIEVAL SYSTEM
• Common Device Name: Laparoscope, general plastic surgery
• Manufacturer (Section D): Conmed Corporation; 525 french rd; utica NY 13502
• MDR Report Key: 50112722
• Report Number: 50112722
• Device Sequence Number: 18722317
• Product Code: GCJ
• UDI-Device Identifier: 20653405986147
• UDI-Public: (01)20653405986147
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: User Facility
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 07/27/2026
• Report Date (Section F): 07/27/2026

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: Other
• Device Model Number: TRS-ROBO-8
• Device Catalogue Number: TRS-ROBO-8
• Device Lot Number: 202601065
• Was Device Available for Evaluation?: No
• Date Returned to Manufacturer: 06/15/2026
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: Yes
• Event Location: Hospital
• Date Report to Manufacturer: 08/03/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 08/03/2026
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Male
• Date Report Sent to FDA: 07/27/2026