MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2018-12-04 for BIOGLUE SURGICAL ADHESIVE BG3502-5-G manufactured by Cryolife, Inc. ? Kennesaw.
[129226185]
This investigation is currently ongoing. Any additional information will be provided in the follow-up report.
Patient Sequence No: 1, Text Type: N, H10
[129226186]
According to initial reports, during a recent cervical discectomy surgi-flo was used to gain haemostasis. A few drops of bg were then applied to seal a small csf leak. Subsequently the surgeon found a "clot" or amalgam which required removal - this was achieved relatively easily using a surgical hook.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1063481-2018-00049 |
MDR Report Key | 8129460 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2018-12-04 |
Date of Report | 2019-02-18 |
Date of Event | 2018-11-22 |
Date Facility Aware | 2018-11-22 |
Date Mfgr Received | 2018-11-22 |
Date Added to Maude | 2018-12-04 |
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 SURGICAL ADHESIVE |
Generic Name | GLUE,SURGICAL,ARTERIES |
Product Code | MUQ |
Date Received | 2018-12-04 |
Model Number | BG3502-5-G |
Lot Number | UNKNOWN |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CRYOLIFE, INC. ? KENNESAW |
Manufacturer Address | 1655 ROBERTS BLVD KENNESAW GA 30144 US 30144 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2018-12-04 |