MAUDE Adverse Event Report: WICKIMED SUPPLY COMPANY LIMITED PLUMEPEN ELITE SURGICAL SMOKE EVAC PENCIL, 15FT TUBING,QTY20; ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Catalog Number PLP2520

Device Problem Break (1069)

Patient Problem Burn(s) (1757)

Event Date 02/08/2024

Event Type  Injury  

Manufacturer Narrative

The device is not expected to be returned for evaluation and review.However, the complaint investigation is not complete at this time.A supplemental and final report will be filed following the completion of the complaint investigation.We will continue to monitor for trends through the complaint system to assure patient safety.

Event Description

The sales representative reported on behalf of the customer, that the plp2520 plumepen elite surgical smoke evac pencil, 15ft tubing,qty (b)(4) was being used during an unknown procedure on (b)(6) 2024 when it was reported ¿the button broke on the pencil causing it to remain on and burn the patient.¿.Further assessment questions were requested of the reporter and a good faith effort was completed; however, the reporter has not responded to our attempts for information.There was no report of medical intervention, or hospitalization for the patient.This report is being raised on reported injury due to unknown degree of burn.

Manufacturer Narrative

Received one plp2520 in opened original packaging.Lot number was verified.Performed a visual inspection, the coagulation button is concaved within the handpiece creating continuous connection with the circuit board.Performed a functional inspection using the esu system 7550 (c8406), the device continuously activates when plugged in without pressing the button.The root cause cannot be determined, however, based upon evaluation, the likely cause of this event was electrical shorting due to water ingression into the device.The manufacturing documents from the device history record have been reviewed with special attention to the manufacturing and inspection of the product.The product released for distribution was found to have met all specifications prior to shipment.This is the only complaint for this lot number and failure mode within the past two years.(b)(4).Per the instructions for use, the user is advised to inspect instruments and cables for damage prior to each use, especially the insulation of laparoscopic/endoscopic instruments.The electrode tip may remain hot enough to cause burns after the current has been de-activated.Inadvertent activation or movement of the activated electrode outside of the field of vision may result in injury to the patient.Localized burns to the patient or physician may result from electrical currents carried through conductive objects.We will continue to monitor for trends through the complaint system to assure patient safety.

Event Description

The sales representative reported on behalf of the customer, that the plp2520 plumepen elite surgical smoke evac pencil, 15 ft tubing, qty (b)(4) was being used during an unknown procedure on (b)(6) 2024 when it was reported ¿the button broke on the pencil causing it to remain on and burn the patient.¿.Further assessment questions were requested of the reporter and a good faith effort was completed; however, the reporter has not responded to our attempts for information.There was no report of medical intervention, or hospitalization for the patient.This report is being raised on reported injury due to unknown degree of burn.

• Brand Name: PLUMEPEN ELITE SURGICAL SMOKE EVAC PENCIL, 15FT TUBING,QTY20
• Type of Device: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
• Manufacturer (Section D): WICKIMED SUPPLY COMPANY LIMITED; 4-5/f, building b; tangjiao industrial area; lilin, huizhou, prc china 51600 0; CH 516000
• Manufacturer (Section G): WICKIMED SUPPLY COMPANY LIMITED; 4-5/f, building b; tangjiao industrial area; lilin, huizhou, prc china 51600 0; CH 516000
• Manufacturer Contact: samantha dewberry ; 525 french road; utica, NY 13502 ; 3152230184
• MDR Report Key: 18844712
• MDR Text Key: 336964150
• Report Number: 1320894-2024-00052
• Device Sequence Number: 1
• Product Code: GEI
• UDI-Device Identifier: 108458854061305
• UDI-Public: (01)108458854061305(17)260129(10)WM20230117
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K230547
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: User Facility,Company Representative
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 04/12/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/06/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: PLP2520
• Device Lot Number: WM20230117
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 04/11/2024
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 01/30/2023
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Other
• Patient Ethnicity: Non Hispanic