MAUDE Adverse Event Report: Microline Surgical, Inc. ReNew Reuseable Long Fenestrated Grasper Tip; Manual Detachable Surgical Instruments

Model Number	3261
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/28/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
The tip broke inside of patient, all pieces were retrieved and patient is doing well.
Additional Manufacturer Narrative
Microline is awaiting return of the device so an investigation can be performed.

• Brand Name: ReNew Reuseable Long Fenestrated Grasper Tip
• Common Device Name: Manual Detachable Surgical Instruments
• Manufacturer (Section D): Microline Surgical, Inc.; 50 dunham rd; suite 1500; beverly MA 01915
• Manufacturer (Section G): Microline Surgical; 50 dunham rd; suite 1500; beverly MA 01915
• Manufacturer Contact: scott marchand-davis ; 50 dunham rd; suite 1500; beverly, MA 01915
• MDR Report Key: 50116233
• Report Number: 1223422-2026-00008
• Device Sequence Number: 10039954
• Product Code: GEI
• UDI-Device Identifier: 00811099011699
• UDI-Public: 00811099011699
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K974066
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 08/03/2026

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: 3261
• Device Catalogue Number: 3261
• Device Lot Number: Unknown
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/28/2026
• Initial Report FDA Received Date: 08/03/2026
• 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
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown