BIOGLUE SYRINGE 5-PACK, 10ML BG3510-5-J

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2019-05-24 for BIOGLUE SYRINGE 5-PACK, 10ML BG3510-5-J manufactured by Cryolife, Inc..

Event Text Entries

[146075160] This investigation is currently ongoing. Any additional information will be provided in the follow-up report.
Patient Sequence No: 1, Text Type: N, H10


[146075161] Incidence of postoperative pyrexia of about 38 degrees has been observed after 2-3 weeks from the time of operation. It was considered to be infection-attributable in the beginning, but white blood cell count is stable and inflammation was within the normal range, the doctor now considers it might be bioglue-related. Bioglue was applied to false lumen, suture lines at aortic root as well as distal aortic arch.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1063481-2019-00031
MDR Report Key8640662
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2019-05-24
Date of Report2019-07-03
Date Facility Aware2019-05-15
Date Mfgr Received2019-05-15
Date Added to Maude2019-05-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactROCHELLE MANEY
Manufacturer Street1655 ROBERTS BLVD.
Manufacturer CityKENNESAW GA 30144
Manufacturer CountryUS
Manufacturer Postal30144
Manufacturer Phone7704193355
Manufacturer G1CRYOLIFE, INC.
Manufacturer Street1655 ROBERTS BLVD. NW
Manufacturer CityKENNESAW GA 30144
Manufacturer CountryUS
Manufacturer Postal Code30144
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIOGLUE SYRINGE 5-PACK, 10ML
Generic NameGLUE,SURGICAL,ARTERIES
Product CodeMUQ
Date Received2019-05-24
Model NumberBG3510-5-J
Lot Number18EJX001
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCRYOLIFE, INC.
Manufacturer Address1655 ROBERTS BLVD. NW KENNESAW GA 30144 US 30144


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-05-24

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