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..
[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
Report Number | 1063481-2019-00031 |
MDR Report Key | 8640662 |
Report Source | DISTRIBUTOR,FOREIGN,HEALTH PR |
Date Received | 2019-05-24 |
Date of Report | 2019-07-03 |
Date Facility Aware | 2019-05-15 |
Date Mfgr Received | 2019-05-15 |
Date Added to Maude | 2019-05-24 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | ROCHELLE MANEY |
Manufacturer Street | 1655 ROBERTS BLVD. |
Manufacturer City | KENNESAW GA 30144 |
Manufacturer Country | US |
Manufacturer Postal | 30144 |
Manufacturer Phone | 7704193355 |
Manufacturer G1 | CRYOLIFE, INC. |
Manufacturer Street | 1655 ROBERTS BLVD. NW |
Manufacturer City | KENNESAW GA 30144 |
Manufacturer Country | US |
Manufacturer Postal Code | 30144 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BIOGLUE SYRINGE 5-PACK, 10ML |
Generic Name | GLUE,SURGICAL,ARTERIES |
Product Code | MUQ |
Date Received | 2019-05-24 |
Model Number | BG3510-5-J |
Lot Number | 18EJX001 |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CRYOLIFE, INC. |
Manufacturer Address | 1655 ROBERTS BLVD. NW KENNESAW GA 30144 US 30144 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-05-24 |