MAUDE Adverse Event Report: COVIDIEN LLC MAHURKAR ELITE; CATHETER, HEMODIALYSIS, NON-IMPLANTED

Model Number	8888222220
Medical Device Problem Codes	Product Quality Problem (1506); Unraveled Material (1664)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	05/07/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
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.
Event or Problem Description
According to the reporter, during procedure, the distributor reports that their client was having a trouble with the guide wire bending.There was no reported patient outcome.
Additional Manufacturer Narrative
Additional information: g3, h3, h6 h3 evaluation summary: mozarc medical conducted an investigation based upon all information received.The involved device was not returned.However, a video was provided.Visual inspection noted that one guidewire, that was visibly coiled and bent.There appeared to be no other abnormalities with the device.It was reported that the guide wire was frayed and had issue.The reported issues were confirmed.The most likely cause could not be established from the information available.The manufacturing records for each device are thoroughly reviewed prior to release to ensure that it meets all mozarc medicalquality specifications.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.
Event or Problem Description
According to the reporter, during procedure, the distributor reports that their client was having trouble with the guide wire bending with difficulty, the guidewire became stuck in the lumen.The guidewire was still intact.Nothing¿unusual was observed on the device prior to use.There were no other products being utilized with the device.There was no excessive force use on the device.Besides the reported issue, there were no visible defects/damages found on the product at the time of the event.There was no remedial action with the reported product, however the procedure was completed using guidewire from a different brand of catheter.There was no reported patient outcome.
Additional Manufacturer Narrative
Additional information: b5, e, g3 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.
Additional Manufacturer Narrative
Additional information: g3 correction: b5 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.
Event or Problem Description
According to the reporter, during procedure, the distributor reports that their client was having trouble with the guide wire bending with difficulty, the guidewire became stuck in the lumen and coiled.The guidewire was still intact.Nothing¿unusual was observed on the device prior to use.There were no other products being utilized with the device.There was no excessive force use on the device.Besides the reported issue, there were no visible defects/damages found on the product at the time of the event.There was no remedial action with the reported product, however the procedure was completed using guidewire from a different brand of catheter.There was no reported patient outcome.

• Brand Name: MAHURKAR ELITE
• Common Device Name: CATHETER, HEMODIALYSIS, NON-IMPLANTED
• Manufacturer (Section D): COVIDIEN LLC; 15 hampshire st; mansfield MA 02048
• Manufacturer (Section G): COVIDIEN LLC; 15 hampshire st; mansfield MA 02048
• Manufacturer Contact: barbara lancini ; via camurana, 1; mirandola,mo 41037 ; IT 41037 ; 472677862
• MDR Report Key: 25142209
• Report Number: 1282497-2026-00027
• Device Sequence Number: 9406760
• Product Code: MPB
• UDI-Device Identifier: 10884521125841
• UDI-Public: (01)10884521125841(17)300731(10)252230203(20)01
• Combination Product (Y/N): N
• Initial Reporter Country: MX
• PMA/510(K) Number: K120674
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative,Distributor
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 05/27/2026

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 Model Number: 8888222220
• Device Catalogue Number: 8888222220
• Device Lot Number: 252230203
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/08/2026
• Supplement Date Received by Manufacturer: 05/12/2026; 05/17/2026; 05/20/2026
• Initial Report FDA Received Date: 05/11/2026
• Supplement Report FDA Received Date: 05/13/2026; 05/18/2026; 05/27/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 08/11/2025
• 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
• Patient Sex: Unknown