MAUDE Adverse Event Report: APPLIED MEDICAL RESOURCES KII OPTICAL ACCESS SYSTEM; LAPAROSCOPE, GENERAL & PLASTIC SURGERY

Model Number	C0R37
Medical Device Problem Code	Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/10/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The event unit is anticipated to return to applied medical for evaluation.A follow-up report will be sent upon completion of investigation.
Event or Problem Description
Procedure performed: robotic pulmonary lobectomy.Event description: complaint 1 of 2 - (b)(4), complaint 2 of 2 - (b)(4).[translation] during a robotic pulmonary lobectomy in room 1 of the general ward, the internal reducing valve of the the internal reducing valve of the 15 mm trocar on repeated passage of the instruments, on 2 occasions (2 trocars used from 2 different batches).Disconnection of the valve components from the 1st trocar, part of which fell into the thoracic cavity.Search for the part of the valve from the 1st trocar used that fell into the thoracic cavity.2nd trocar valve before disconnecting its components.Actions taken in the care facility to manage the patient: find the valve that has fallen into the patient's thorax and removal.Type of intervention: removed the valve.Patient status: patient is ok.
Event or Problem Description
Procedure performed: robotic pulmonary lobectomy.Event description: complaint 1 of 2 - (b)(4) [batch id: 2027111-20250210093621].Complaint 2 of 2 - (b)(4) [batch id: 2027111-20250210093754].[translation] during a robotic pulmonary lobectomy in room 1 of the general ward, the internal reducing valve of the internal reducing valve of the 15 mm trocar on repeated passage of the instruments, on 2 occasions (2 trocars used from 2 different batches).Disconnection of the valve components from the 1st trocar, part of which fell into the thoracic cavity.Search for the part of the valve from the 1st trocar used that fell into the thoracic cavity.2nd trocar valve before disconnecting its components.Actions taken in the care facility to manage the patient: find the valve that has fallen into the patient's thorax and removal.Type of intervention: removed the valve.Patient status: patient is ok.
Additional Manufacturer Narrative
The event unit was not returned to applied medical for evaluation.As the event unit was not returned, applied medical is unable to determine if the event unit exhibited any non-conformances that could have contributed to the reported event.Based on the description of the event, it is likely that the dislodged shield and fragmented seal components were caused by an asymmetrical instrument that was inserted in a non-axial manner.Applied medical¿s instructions for use (ifu) states that, ¿extra care should be used when inserting angular and asymmetrical instruments, such as ¿j¿ hooks and clip appliers.All instruments should be centered axially when inserted through the seal to prevent tearing¿ applied medical has performed a historical trend analysis and review of production records and no relevant documentation was identified.

• Brand Name: KII OPTICAL ACCESS SYSTEM
• Common Device Name: LAPAROSCOPE, GENERAL & PLASTIC SURGERY
• Manufacturer (Section D): APPLIED MEDICAL RESOURCES; 22872 avenida empresa; rancho santa margarita CA 92688
• Manufacturer Contact: ashleigh mendez ; 22872 avenida empresa; rancho santa margarita, CA 92688 ; 9497135359
• MDR Report Key: 21345390
• Report Number: 2027111-2025-00355
• Device Sequence Number: 12752343
• Product Code: GCJ
• UDI-Device Identifier: 00607915116422
• UDI-Public: (01)00607915116422
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• PMA/510(K) Number: K060096
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Pharmacist
• Type of Report: Initial,Followup
• Report Date (Section B): 07/09/2025

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 Model Number: C0R37
• Device Catalogue Number: 101414401
• Device Lot Number: 1512626
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/27/2025
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 02/10/2025
• Supplement Report FDA Received Date: 07/09/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 03/07/2024
• 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: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown