MAUDE Adverse Event Report: ORIDION MEDICAL MICROSTREAM; ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE

Model Number CS08651-02

Device Problem Device Difficult to Program or Calibrate (1496)

Patient Problems Injury (2348); No Known Impact Or Consequence To Patient (2692)

Event Date 05/02/2018

Event Type  Injury  

Manufacturer Narrative

If information is provided in the future, a supplemental report will be issued.

Event Description

According to the reporter, the device flashed required calibration and did not work properly.The customer indicated that the patient was hospitalized over the weekend due to malfunction.

Manufacturer Narrative

If information is provided in the future, a supplemental report will be issued.

Manufacturer Narrative

Correction: (pt.Identifier), (rpt.Sent to fda?), (patient codes).Medtronic, inc.(medtronic) is submitting this report to comply with 21 c.F.R.Part 803, the medical device reporting regulation.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 in the time allotted and has provided as much information as is available to the company as of the submission date this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic or its employees 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 reporting pursuant to part 803.Medtronic objects to the use of these words and others like it 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.

Event Description

According to the reporter, the device flashed required calibration and did not work properly.The customer indicated that the patient was hospitalized over the weekend due to malfunction.An update was received and the hospitalization of the patient was not related to the unit.Patient current status was unknown.

Manufacturer Narrative

Additional information: evaluation summary: one unit was returned and showed the calibration required message.Ac (alternating current) power was connected and unit was powered up and passed post (power on self-test).During post, the welcome screen showed the calibration being overdue.The monitoring screen showed the calibration required message in the information area.System was checked and showed 27345 hours left before service and 0 hours left before calibration.The service menu was entered.Date of last calibration in the system was december 9, 2014.Manufacturing label on the side of the device showed that it was manufactured in november of 2014.Operator's manual was checked and it is recommended that the first calibration be performed at 1200 operating hours or 12 months, and all subsequent calibrations performed at 4000 operating hours or 12 months.Manual states it recommends calibration within two weeks of the calibration required message.A test filterline was connected.Unit was able to monitor technician's breath for approximately 10 minutes with no issues or alarms.Tech services was consulted to determine if further customer or owning facility education was required.Received a response that the customer and facility have been educated.Medtronic, inc.(medtronic) is submitting this report to comply with 21 c.F.R.Part 803, the medical device reporting regulation.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 in the time allotted and has provided as much information as is available to the company as of the submission date this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic or its employees 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 reporting pursuant to part 803.Medtronic objects to the use of these words and others like it 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: MICROSTREAM
• Type of Device: ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE
• Manufacturer (Section D): ORIDION MEDICAL; 7 hamarpeh st.; jerusalem 91235
• MDR Report Key: 7534869
• MDR Text Key: 108949751
• Report Number: 8044004-2018-00008
• Device Sequence Number: 1
• Product Code: CCK
• UDI-Device Identifier: 10884521551480
• UDI-Public: 10884521551480
• Combination Product (y/n): N
• PMA/PMN Number: K112368
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: user facility
• Type of Report: Initial,Followup,Followup,Followup
• Report Date: 10/04/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: CS08651-02
• Device Catalogue Number: CS08651-02
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/23/2018
• Initial Date Manufacturer Received: 05/16/2018
• Initial Date FDA Received: 05/22/2018
• Supplement Dates Manufacturer Received: 05/16/2018; 06/12/2018; 08/08/2018
• Supplement Dates FDA Received: 05/24/2018; 07/09/2018; 10/04/2018
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Hospitalization
• Patient Age: 34 YR