MAUDE Adverse Event Report: TERUMO CORPORATION, ASHITAKA CAPIOX FX25 OXYGENATOR; OXYGENATOR, CARDIOPULMONARY BYPASS

Model Number N/A

Device Problem Infusion or Flow Problem (2964)

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

Event Date 06/21/2022

Event Type  malfunction  

Manufacturer Narrative

Implanted date: device was not implanted.Explanted date: device was not explanted.Healthcare professional - unknown.Occupation - others.Pma/510(k)- k130520.The actual sample was discarded by the user facility; therefore, an evaluation of the actual device was unable to be performed.Review of the provided pump record obtained the following findings" · the circulation conditions (blood flow rate, gas flow rate, and fio2) were the same at 14:50 and at 15:50, though at 14:50, svo2 was 82% and pao2 was 23.9, at 15:50, svo2 was 89% and pao2 had decreased to 15.9.· the lowest po2 was 10.8 at 16:50.The next measurement performed at 17:20 indicated that pao2, svo2 and paco2 had increased.Np °c at 17:20 was logged as 36.7°c.In the event section of the record, it was stated that cooling started at 17:18.From this, it was considered that the patient's o2 consumption decreased leading to increasing svo2.In addition, when the blood temperature decreased, the removal of co2 became difficult, leading to increasing paco2 accordingly.· the blood temperature was found to have decreased to 32.9°c at 17:35, and then increased at 17:50.At that moment, pao2 and svo2 was found to have decreased.Review of the manufacturing record and the product-release judgement record of the involved product/lot# combination confirmed there was no anomaly in them.A search of the complaint file found no similar report from the same facility regarding the involved product code/lot# combination.From the investigation results, no anomaly was found in the manufacturing records.Since no actual sample was available, close analysis could not be performed, the definite cause of occurrence could not be determined.From the pump record, in which it was logged that pao2 was low before the rewarming started, one of possible causes was inferred to be a combination of the wet lung phenomenon compromising the gas exchange performance and the change in pao2 due to the change in the patient's temperature.Ifu states: "upon patient rewarming, adjust o2 concentration, gas flow rate and blood flow rate by increasing them as needed based on an increase in patient's metabolism.Failure to adjust the gas supply and the blood flow rate appropriately may cause insufficient o2 supply needed or the amount of the patient's gaseous metabolism.- during circulation, always carefully monitor the patient blood condition and the oxygenator gas exchange performance.If gas exchange performance deteriorates, temporarily raise the gas flow rate to flush the inside of the fiber and try to recover performance.- the gas flow rate for flushing is 20 l / min, the time is 10 seconds.If the performance does not recover immediately, it is considered to be caused by plasma leak.Therefore, replace this product with a new one without repeating the flush." (b)(4).

Event Description

The user facility reported that the patient had been on bypass for five hours with no unusual incidents however the po2 was extremely low on rewarming eventually resulting in a po2 of 7mmhg with an fio2 of 100%.The case was quite complex and unique which required an extracorporeal membrane oxygenation (ecmo) machine in theatre which the patient was placed onto with no harm occurring (it was always the plan to initiate extracorporeal membrane oxygenation (ecmo)).It was not necessary to re-establish cardiopulmonary bypass.There was no need for medical intervention and the procedure was performed as intended.The oxygenator was not replaced as we went onto extracorporeal membrane oxygenation (ecmo) as planned.There was no additional impact on the patient as a result and the patient was not harmed.The procedure outcome was not reported.

• Brand Name: CAPIOX FX25 OXYGENATOR
• Type of Device: OXYGENATOR, CARDIOPULMONARY BYPASS
• Manufacturer (Section D): TERUMO CORPORATION, ASHITAKA; 150 maimaigi-cho; fujinomiya city, 418 ; JA 418
• Manufacturer (Section G): TERUMO CORPORATION, ASHITAKA; reg. no. 9681834; 150 maimaigi-cho; fujinomiya city, 418 ; JA 418
• Manufacturer Contact: stephanie handy ; reg. no. 2243441; 950 elkton blvd.; elkton, MD 21921 ; 9499890491
• MDR Report Key: 15036809
• MDR Text Key: 304796676
• Report Number: 9681834-2022-00133
• Device Sequence Number: 1
• Product Code: DTZ
• UDI-Device Identifier: 04987350701022
• UDI-Public: 04987350701022
• Combination Product (y/n): N
• Reporter Country Code: UK
• PMA/PMN Number: K071494
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,User Facility,Company Representative
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 07/17/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/17/2022
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: CX*FX25RE
• Device Lot Number: 220131
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 06/22/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 01/31/2022
• 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
• Patient Age: 21 YR
• Patient Sex: Female
• Patient Weight: 65 KG