MAUDE Adverse Event Report: MICROLINE SURGICAL INC MINI ENDOCUT SCISSOR TIP, DISPOSABLE; FLEXIBLE ENDOSCOPIC SCISSORS, SINGLE-USE

Model Number	3152
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/10/2024
Type of Reportable Event	Malfunction
Event or Problem Description
The heat shrink fell into the abdominal cavity and was retrieved.
Additional Manufacturer Narrative
At this time, microline surgical is awaiting the suspected device back so an investigation can be conducted.Once the results of the investigation are available, a final adverse event report will be submitted.

• Brand Name: MINI ENDOCUT SCISSOR TIP, DISPOSABLE
• Common Device Name: FLEXIBLE ENDOSCOPIC SCISSORS, SINGLE-USE
• Manufacturer (Section D): MICROLINE SURGICAL INC; 50 dunham rd suite 1500; beverly MA 01915
• Manufacturer (Section G): MICROLINE SURGICAL INC; 50 dunham rd suite 1500; beverly MA 01915
• Manufacturer Contact: scott marchand davis ; 50 dunham rd suite 1500; beverly, MA 01915 ; 9789229810
• MDR Report Key: 21018736
• Report Number: 1223422-2024-00050
• Device Sequence Number: 4120727
• Product Code: GEI
• UDI-Device Identifier: 00811099010012
• UDI-Public: 00811099010012
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K213127
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 12/26/2024

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 Model Number: 3152
• Device Catalogue Number: 3152
• Device Lot Number: 0017072000811099010012
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/23/2024
• Initial Report FDA Received Date: 12/26/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown