QUADROX-ID BIOLINE OXYGENATOR 701067859 BEQ-HMOD70000-USA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-18 for QUADROX-ID BIOLINE OXYGENATOR 701067859 BEQ-HMOD70000-USA manufactured by Getinge Group / Maquet Cardiopulmonary Gmbh.

Event Text Entries

[131374560] Maquet medical systems usa ref# (b)(4), bioline quadrox oxygenators-no clamp, used in conjunction with the following devices to encompass a system. Issues noted following the change in mfr's specs that began in (b)(6) 2018. Please note that the following info is in ref to the newest design and have not seen this issue with the previous design. Using standard priming technique per mfr ifu, when the oxygenator is primed with plasmalyte, the oxygenator appears primed correctly, per our policy the device is then stored for no more than 30 days to be ready for use in an emergency if needed. During the 30-day window, it has been noted that the fluid level in the oxygenator is deprimed 1-2 inches below the deaeration port on the venous side. The deaeration port remains capped, with no ports open and no fluid puddles found. Oxygenator is off and prime lines closed. When primed with blood for use on a pt, we see venous side of the oxygenator suddenly become deprimed requiring add'l blood after priming is already complete. No other source air is noted on the venous side, nor in the priming line. The arterial side is noted to be priming from the bottom up with the top portion not primed. The top portion will only prime once fluid is pulled off the pigtail at the top of the oxygenator. Pre and post pressures are not affected and oxygenator appears to be functioning appropriately. Once in pt use, thrombus formation is noted in less than 24 hours after initial prime, at the top of the arterial side in the same area that was difficult to prime. After discussing the issue via phone with the getinge clinical specialist and account mgr, an email was prepared and sent on (b)(6) 2018 with our observation. On (b)(6) 2018, the vendor was contacted again and an add'l email sent with another instance of the event, this circuit was drained, saved, and made available to the mfr for investigation. This was picked up by the rep on (b)(6) 2018. During the visit by both getinge clinical specialist and the account rep, we were able to blood prime an add'l plasmalyte circuit, that was showing signs of issue (depriming while sitting) the blood prime was videotaped as part of the investigation by getinge. During the blood prime, the same issues, we are reporting occurred. The oxygenator was then drained and sent with the rep for investigation. Our concern at this time as the vendor has not been able to identify the defect that if this issue occurs without being caught prior to placement on a pt, it could cause severe injury or death to the pt. This issue is adding unexpected delay to pt care in time sensitive situations. All correspondence has been saved, video and photos of priming issues are available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5082269
MDR Report Key8180385
Date Received2018-12-18
Date of Report2018-12-17
Date of Event2018-12-17
Date Added to Maude2018-12-19
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Sequence Number: 0

Brand NameQUADROX-ID BIOLINE OXYGENATOR
Generic NameFILTER BLOOD CARDIOPULMONARY BYPASS ARTERIAL LINE
Product CodeDTZ
Date Received2018-12-18
Returned To Mfg2018-12-04
Model Number701067859
Catalog NumberBEQ-HMOD70000-USA
Lot Number(MULTIPLE)
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrI
Device Sequence No0
Device Event Key0
ManufacturerGETINGE GROUP / MAQUET CARDIOPULMONARY GMBH

Device Sequence Number: 1

Brand NameQUADROX-ID BIOLINE OXYGENATOR
Generic NameFILTER BLOOD CARDIOPULMONARY BYPASS ARTERIAL LINE
Product CodeDTM
Date Received2018-12-18
Returned To Mfg2018-12-04
Model Number701067859
Catalog NumberBEQ-HMOD70000-USA
Lot Number(MULTIPLE)
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerGETINGE GROUP / MAQUET CARDIOPULMONARY GMBH


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-18

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