MAUDE Adverse Event Report: TELEFLEX MEDICAL WECK AUTO ENDO5 ML; CLIP, IMPLANTABLE

Catalog Number	AE05ML
Medical Device Problem Codes	Failure to Fire (2610); Material Twisted/Bent (2981)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/24/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).
Event or Problem Description
It was reported that "clips were not firing." no medical intervention required.The patient status is reported as "fine.".
Event or Problem Description
It was reported that "clips were not firing." no patient involvement.".
Additional Manufacturer Narrative
(b)(4) complaint verification testing could not be performed as no sample was returned for analysis.A device history record review was performed, and no relevant findings were identified.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.If the sample becomes available at a later date a follow-up report will be submitted with investigation results.Teleflex will continue to monitor and trend for reports of this nature.Other remarks: n/a corrected data: section a: patient identifier updated from "unknown" to "n/a." section b: updated from "it was reported that "clips were not firing." no medical intervention required.The patient status is reported as "fine."" to "it was reported that "clips were not firing." no patient involvement." relevant tests/laboratory data, including dates updated from "none reported." to "n/a." other relevant history, including preexisting medical conditions updated from "none reported." to "n/a." section d: concomitant medical products and therapy dates updated from "none reported." to "n/a." section h: health effect - impact code updated from "2199" to "2645.".
Additional Manufacturer Narrative
(b)(4).Upon review of the investigation report for the returned sample, it was determined that the event does not meet the criteria for reportability.Therefore, the initial mdr submitted on 20 march 2026 should be retracted.Complaint verification testing could not be performed as no sample was returned for analysis.A device history record review was performed, and no relevant findings were identified.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.If the sample becomes available at a later date a follow-up report will be submitted with investigation results.Teleflex will continue to monitor and trend for reports of this nature.Other remarks: n/a.Corrected data: section a: patient identifier updated from "unknown" to "n/a." section b: updated from "it was reported that "clips were not firing." no medical intervention required.The patient status is reported as "fine."" to "it was reported that "clips were not firing." no patient involvement." relevant tests/laboratory data, including dates updated from "none reported." to "n/a." other relevant history, including preexisting medical conditions updated from "none reported." to "n/a." section d: concomitant medical products and therapy dates updated from "none reported." to "n/a." section h: health effect - impact code updated from "2199" to "2645.".
Event or Problem Description
It was reported that "clips were not firing." no patient involvement.".

• Brand Name: WECK AUTO ENDO5 ML
• Common Device Name: CLIP, IMPLANTABLE
• Manufacturer (Section D): TELEFLEX MEDICAL; morrisville NC
• Manufacturer (Section G): TELEFLEX MEDICAL; rancho el descanso; tecate 21478 ; MX 21478
• Manufacturer Contact: laura guadalupe gonzalez ; 3015 carrington mill blvd; morrisville, NC 27560
• MDR Report Key: 24655944
• Report Number: 3003898360-2026-00145
• Device Sequence Number: 5726808
• Product Code: FZP
• UDI-Device Identifier: 14026704741868
• UDI-Public: (01)14026704741868(11)250315(17)260912(10)73C2500439(21)
• Combination Product (Y/N): N
• Initial Reporter Country: KS
• PMA/510(K) Number: K230480
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,User Facility,Distributor
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 02/24/2026

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 Expiration Date: 09/12/2026
• Device Catalogue Number: AE05ML
• Device Lot Number: 73C2500439
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/24/2026
• Supplement Date Received by Manufacturer: 03/09/2026; 04/28/2026
• Initial Report FDA Received Date: 03/20/2026
• Supplement Report FDA Received Date: 03/20/2026; 04/30/2026
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 03/15/2025
• 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: NONE REPORTED.
• Patient Sex: Unknown