MAUDE Adverse Event Report: MEDTRONIC, INC EVEREST INFLATION DEVICE; ADAPTOR, STOPCOCK, MANIFOLD, FITTING, CARDIOPULMONARY BYPASS

Model Number AC2200

Device Problem Defective Device (2588)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 07/21/2022

Event Type  malfunction  

Event Description

One everest inflation device was attempted to be used.There was no damage noted to the packaging.The device was removed from the packaging per ifu with no issues noted.The device was inspected and prepped per ifu with no issues noted.The in-deflator was connected to a balloon and stent device when the issue occurred.There was no stopcock connected between the everest and the other devices.It was reported that a manometer issue occurred.At first the needle was unresponsive at 0 atm and didn't react.As the needle of the manometer did not react, it was not possible to see the given pressure.The needle of the manometer then jumped up to 12-14 atm.It was reported that the device was not used in the patient.It was subsequently reported that the event occurred during use in the patient.The procedure was completed successfully with the reported everest device.No patient injury reported.

Manufacturer Narrative

Product analysis review: the lot number matches details in the complaint file.1 everest inflation device returned for analysis.No damage was noted to the syringe body, tube, joints or manometer housing.The device was returned with a volume of clear liquid remaining in the syringe chamber and was expressed with no issues noted.As received the gauge needle was at approx.0 atm.Using an in-house stopcock, the device was pressurised with water.On pressurisation of the device the needle remained stuck at 0 atm while turning the piston knob, then it jumped to approx.12 atm and rose steadily to 30 atm.The device held pressure for a minimum of 3 minutes (with max 10% loss), meeting specification.Upon release of pressure the gauge needle dropped to approx.1.5 atm.When vacuum was applied, the gauge needle did not move into the red "vac" reading.Medtronic is submitting this report to comply with fda reporting regulations under 21 cfr parts 4 and 803.This report is based upon information obtained by medtronic, which the company may not have been able to fully investigate or verify prior to the date the report was required by the fda.Medtronic has made reasonable efforts to obtain more complete information and has provided 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.In particular, this report does not constitute an admission by anyone that the product described in this report has any ¿defects¿ or has ¿malfunctioned¿.These words are included in the fda 3500a form and are fixed items for selection created by the fda to categorize the type of event solely for the purpose of regulatory reporting.Medtronic objects to the use of these words and others like them because of the lack of definition and the connotations implied by these terms.This statement should be included with any information or report disclosed to the public under the freedom of information act.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.

Manufacturer Narrative

Additional information: annex d code.Medtronic is submitting this report to comply with fda reporting regulations under 21 cfr parts 4 and 803.This report is based upon information obtained by medtronic, which the company may not have been able to fully investigate or verify prior to the date the report was required by the fda.Medtronic has made reasonable efforts to obtain more complete information and has provided 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.In particular, this report does not constitute an admission by anyone that the product described in this report has any ¿defects¿ or has ¿malfunctioned¿.These words are included in the fda 3500a form and are fixed items for selection created by the fda to categorize the type of event solely for the purpose of regulatory reporting.Medtronic objects to the use of these words and others like them because of the lack of definition and the connotations implied by these terms.This statement should be included with any information or report disclosed to the public under the freedom of information act.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.

• Brand Name: EVEREST INFLATION DEVICE
• Type of Device: ADAPTOR, STOPCOCK, MANIFOLD, FITTING, CARDIOPULMONARY BYPASS
• Manufacturer (Section D): MEDTRONIC, INC; 37a cherry hill dr; danvers MA 01923
• Manufacturer (Section G): MEDTRONIC, INC; 37a cherry hill dr; danvers MA 01923
• Manufacturer Contact: alison sweeney ; parkmore business park west; galway ; EI ; 091708096
• MDR Report Key: 15379758
• MDR Text Key: 300634240
• Report Number: 1220452-2022-00067
• Device Sequence Number: 1
• Product Code: DTL
• UDI-Device Identifier: 00643169843011
• UDI-Public: 00643169843011
• Combination Product (y/n): N
• Reporter Country Code: GM
• PMA/PMN Number: K942269
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Health Professional,Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date: 01/04/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/08/2022
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: AC2200
• Device Catalogue Number: AC2200
• Device Lot Number: 60360075
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/19/2022
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 12/08/2022
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 04/08/2022
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1