MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2016-11-18 for COSEAL 934072 manufactured by Baxter Healthcare - Hayward.
[60416501]
(b)(4). (b)(6). A batch review was conducted and there were no deviations found related to this reported condition during the manufacture of this lot. The device was not received for evaluation; therefore, a device analysis could not be completed. Should additional relevant information become available, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10
[60416502]
It was reported that there were visible particles in the peg syringe of a coseal surgical sealant kit. This occurred after reconstitution, but before patient use. There was no patient involvement. No additional information is available.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1416980-2016-17471 |
MDR Report Key | 6113875 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2016-11-18 |
Date of Report | 2016-11-18 |
Date of Event | 2016-10-22 |
Date Mfgr Received | 2016-10-26 |
Device Manufacturer Date | 2015-10-21 |
Date Added to Maude | 2016-11-18 |
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 Street | 25212 W. ILLINOIS ROUTE 120 |
Manufacturer City | ROUND LAKE IL 60073 |
Manufacturer Country | US |
Manufacturer Postal | 60073 |
Manufacturer Phone | 2242702068 |
Manufacturer G1 | BAXTER HEALTHCARE - HAYWARD |
Manufacturer Street | 2024 W WINTON AVE |
Manufacturer City | HAYWARD CA 94545 |
Manufacturer Country | US |
Manufacturer Postal Code | 94545 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | COSEAL |
Generic Name | SEALANT,POLYMERIZING |
Product Code | NBE |
Date Received | 2016-11-18 |
Model Number | NA |
Catalog Number | 934072 |
Lot Number | HA151037 |
ID Number | NA |
Device Expiration Date | 2016-10-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BAXTER HEALTHCARE - HAYWARD |
Manufacturer Address | HAYWARD CA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2016-11-18 |