MAUDE Adverse Event Report: PERFUSION SYSTEMS CANNULA KIT DLP11W14R DLP; CATHETER, CANNULA AND TUBING, VASCULAR, CARDIO

Model Number	DLP11W14R
Medical Device Problem Codes	Material Puncture/Hole (1504); Material Deformation (2976); Packaging Problem (3007)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/23/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Continuation of d10: product id dlp11w14r (unknown serial/lot); product type: 0183-cannula; 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
Medtronic received information that at an unspecified time, this dlp cannula kit had a crack/break/hole in the packaging.The crack/ break/hole was 4mm in size.The customer also reported a kink just before the y connector.The kink was not in the location of the sutures.The device was replaced to complete the procedure.There was no adverse patient effect reported with this event.
Additional Manufacturer Narrative
Additional information b5.Medtronic received information that during use of a dlp cannula kit the customer reported a crack/break/hole in the packaging.The crack/break/hole was 4mm in size.The customer also reported a kink just before the y connector.The kink was not in the location of the sutures.The device was replaced to complete the procedure.There was no adverse patient effect associated with this event.Medtronic received additional information that there were no missing or wrong devices or components in the package.The issue was observed during the case but not used.Correction d4.2 lot#: this field has been updated.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 b5.Medtronic received information that during use of a dlp cannula kit the customer reported a crack/break/hole in the packaging.The crack/break/hole was 4mm in size.The customer also reported a kink just before the y connector.The kink was not in the location of the sutures.The device was replaced to complete the procedure.There was no adverse patient effect associated with this event.Medtronic received additional information that there were no missing or wrong devices or components in the package.The issue was observed during the case but not used.Correction d4.2 lot#: this field has been updated.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
Medtronic received information that prior to use of a dlp cannula kit, the customer reported a crack/break/hole in the packaging.The crack/break/hole was 4mm in size.The customer also reported a kink just before the y connector.The kink was not in the location of the sutures.The device was replaced.There was no patient involvement, so no adverse effect occurred.Medtronic received additional information that there were no missing or wrong devices or components in the package.Medtronic received additional information that the device was never used on any patient as the issue was discovered when packaging was opened.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
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: CANNULA KIT DLP11W14R DLP
• Common Device Name: CATHETER, CANNULA AND TUBING, VASCULAR, CARDIO
• Manufacturer (Section D): PERFUSION SYSTEMS; 7611 northland dr; brooklyn park MN 55428
• Manufacturer (Section G): PERFUSION SYSTEMS; 7611 northland dr; brooklyn park MN 55428
• Manufacturer Contact: alison sweeney ; parkmore business park west; galway ; EI ; 091708096
• MDR Report Key: 20555090
• Report Number: 2184009-2024-00662
• Device Sequence Number: 18387279
• Product Code: DWF
• UDI-Device Identifier: 00763000644260
• UDI-Public: 00763000644260
• Combination Product (Y/N): N
• Initial Reporter State: WI
• Initial Reporter Country: US
• PMA/510(K) Number: K924529
• 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,Followup,Followup
• Report Date (Section B): 01/30/2025

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 Expiration Date: 07/25/2026
• Device Model Number: DLP11W14R
• Device Catalogue Number: DLP11W14R
• Device Lot Number: 226967356
• 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: 10/25/2024
• Supplement Date Received by Manufacturer: 10/29/2024; 11/22/2024; 01/30/2025
• Initial Report FDA Received Date: 10/29/2024
• Supplement Report FDA Received Date: 11/21/2024; 12/04/2024; 01/30/2025
• Date Device Manufactured: 07/25/2023
• 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