MAUDE Adverse Event Report: I.C. MEDICAL EXTENDEVAC W/ COATED BLADE, 10 FT. TUBING; HOLSTER; ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Model Number	88-000722
Medical Device Problem Codes	Break (1069); Material Fragmentation (1261)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/19/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
A user facility reported, "cautery tip clip is breaking off inside the pencil.Tip is no longer secure and is either sucked up inside the pencil or falls out into the patient." return of the device has been requested, but has not yet been received.A supplier corrective action request (scar) has been sent to the extend evac supplier, i.C.Medical.This mdr represents one of the ten instances described above.This is complaint 6 of 10.This investigation is not complete at this time.No further information is available at this time.We will provide follow-up report when additional information becomes available.
Event or Problem Description
A user facility facility reported, "cautery tip clip is breaking off inside the pencil.Tip is no longer secure and is either sucked up inside the pencil or falls out into the patient.".
Additional Manufacturer Narrative
A distributing facility reported, "inside portion of the pencils has placstick piec that receives electrosurgical tip and that plastic piece is breaking." return of the device was requested, however the involved product was not able to be returned.A supplier corrective action request (scar) has been sent to the extend evac supplier.The supplier reviewed the device history record and found that all failure modes were within the acceptable criteria.Complaint history was also reviewed by the supplier and found to have a low occurrence for this type of complaint.No spec or other manufacturing deviations were found in inventory review.Root cause: because no issues were found with the unused product returned and no issues were found within production records, the root cause could not be determined.Corrective and preventive actions: because no root cause could be determined, no corrective or preventive actions were taken.Deroyal industries ran a complaint to sales ratio from december 2023 to march 2024 and it was found to be 0.00598%.Deroyal will continue to monitor for trends around this item and issue.This investigation is complete at this time.No further information is available at this time.We will provide follow-up report if additional information becomes available.

• Brand Name: EXTENDEVAC W/ COATED BLADE, 10 FT. TUBING; HOLSTER
• Common Device Name: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
• Manufacturer (Section D): I.C. MEDICAL; 15002 n. 25th drive; phoneix AZ 85023
• Manufacturer (Section G): DEROYAL INDUSTRIES, INC.; 1595 highway 33 south; new tazewell TN 37825
• Manufacturer Contact: reagan newman ; 200 debusk lane; powell, TN 37849 ; 8653622106
• MDR Report Key: 19953355
• Report Number: 2320762-2024-00007
• Device Sequence Number: 21068250
• Product Code: GEI
• UDI-Device Identifier: 50749756157914
• UDI-Public: 50749756157914
• Combination Product (Y/N): N
• Initial Reporter State: LA
• Initial Reporter Country: US
• PMA/510(K) Number: K954088
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 08/16/2024

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: 88-000722
• Device Lot Number: 60184438
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/30/2024
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 08/09/2024
• Supplement Report FDA Received Date: 08/19/2024
• 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