MAUDE Adverse Event Report: MEDTRONIC MEXICO S. DE R.L. DE CV PEDIATRIC BIOMEDICUS FEMORAL CANNULA; CATHETER, CANNULA AND TUBING, VASCULAR, CARDIO

Model Number	96820-108
Medical Device Problem Codes	Mechanical Problem (1384); Material Deformation (2976)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/23/2026
Type of Reportable Event	Malfunction
Event or Problem Description
(pli 10, 20, 30, and 40) medtronic received information that prior to use of 3 bio-medicus nextgen pediatric arterial and venous cannula, and 1 bio-medicus arterial life support catheter, it was reported that the obturator was feeling "sticky" in the cannula and it was not going in straight.Customer said it felt like obturator was meeting resistance and it was getting deformed.There was no damage to the packaging.No other devices in the same box/shipping container were damaged.All 4 device's were replaced, and the final cannula felt normal and was used.There was no patient involvement, so no adverse effect occurred.
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.Medtronic will submit a supplemental report if additional relevant information becomes known.
Additional Manufacturer Narrative
Device evaluation summary: visual inspection showed the device was received with the obturator inserted into the cannula with the tip protruding from the cannula tip.Additional visual inspection showed the obturator was deformed inside the cannula.The obturator outer diameter (od) was measured using a keyence scope and the cannula tip inner diameter (id) was measured using a plug gage.The cannula tip id was measured, and it was within specification.The obturator od was measured, and it was within specification.The obturator was inserted and removed several times with no issues noted.The reason for the return was not confirmed.Correction b5: medtronic received information that prior to use of three bio-medicus nextgen pediatric arterial cannulae, and one bi o-medicus arterial life support catheter, it was reported that the obturators were feeling "sticky" in the cannulae and they were not going in straight.The customer said it felt like obturators were meeting resistance and getting deformed.  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: PEDIATRIC BIOMEDICUS FEMORAL CANNULA
• Common Device Name: CATHETER, CANNULA AND TUBING, VASCULAR, CARDIO
• Manufacturer (Section D): MEDTRONIC MEXICO S. DE R.L. DE CV; av. paseo del cucapah #10510; tijuana,bc 22210 ; MX 22210
• Manufacturer (Section G): MEDTRONIC MEXICO S. DE R.L. DE CV; av. paseo del cucapah #10510; tijuana,bc 22210 ; MX 22210
• Manufacturer Contact: alison sweeney ; parkmore business park west; galway ; EI ; 091708096
• MDR Report Key: 24688737
• Report Number: 9617601-2026-02017
• Device Sequence Number: 9653490
• Product Code: DWF
• UDI-Device Identifier: 00763000116293
• UDI-Public: (01)00763000116293(17)300106(10)232995689
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K143083
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 05/07/2026

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: 96820-108
• Device Catalogue Number: 96820-108
• Device Lot Number: 232995689
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/24/2026
• Supplement Date Received by Manufacturer: 04/13/2026
• Initial Report FDA Received Date: 03/25/2026
• Supplement Report FDA Received Date: 05/07/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/06/2026
• 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