MAUDE Adverse Event Report: COVIDIEN PREMIUM SURGICLIP; CLIP, IMPLANTABLE

Model Number	134048
Medical Device Problem Codes	Entrapment of Device (1212); Mechanics Altered (2984)
Health Effect - Clinical Code	Tissue Breakdown (2681)
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that during a laparoscopic hernia procedure, the surgeon was able to squeeze the handle, the clips were unable to load properly into the jaws.It was noted tissues became stuck to the devices when pulling, and the clip remained attached to the device, which tore the vessel after clipping in the three devices.
Additional Manufacturer Narrative
D10 concomitant products: 133650, 133650 premium surgiclip iii 9.0 (lot# p5d1306) 134048, 134048 premium titanium s'clip l (lot# p4k0960).Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.

• Brand Name: PREMIUM SURGICLIP
• Common Device Name: CLIP, IMPLANTABLE
• Manufacturer (Section D): COVIDIEN; sabanetas industrial park; ponce PR 00716 4401
• Manufacturer (Section G): COVIDIEN; sabanetas industrial park; ponce PR 00716 4401
• Manufacturer Contact: mike bocchino ; 8200 coral sea st ne; mounds view, MN 55112-4391 ; 8006464633
• MDR Report Key: 22945981
• Report Number: 2647580-2025-02670
• Device Sequence Number: 9257108
• Product Code: FZP
• UDI-Device Identifier: 10884521057555
• UDI-Public: 10884521057555
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K143644
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 09/02/2025

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: 134048
• Device Catalogue Number: 134048
• Device Lot Number: P4K0960
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/14/2025
• Initial Report FDA Received Date: 09/02/2025
• Date Device Manufactured: 10/07/2024
• 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: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: SEE H11
• Patient Sex: Unknown