MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-30 for VASCULAR PROBES 7451015ES manufactured by Baxter Healthcare - Saint Paul.
[125641745]
The single use device was received for evaluation. Visual inspection revealed particulate matter on the outside of the inner pouch. Microscopic inspection revealed that the particulate matter was a fiber. The size of the fiber was analyzed and was found to be within specifications. The reported condition was not verified. A batch review was conducted and there were no deviations found related to this reported condition during the manufacture of this lot. Should additional relevant information become available, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10
[125641746]
This report summarizes
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1416980-2018-06951 |
MDR Report Key | 8019664 |
Date Received | 2018-10-30 |
Date of Report | 2018-10-30 |
Date Mfgr Received | 2018-09-30 |
Date Added to Maude | 2018-10-30 |
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 | 0 |
Initial Report to FDA | 0 |
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 - SAINT PAUL |
Manufacturer Street | 2575 UNIVERSITY AVE W |
Manufacturer City | SAINT PAUL MN 55114 |
Manufacturer Country | US |
Manufacturer Postal Code | 55114 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | VASCULAR PROBES |
Generic Name | DILATOR, VESSEL, SURGICAL |
Product Code | DWP |
Date Received | 2018-10-30 |
Model Number | NA |
Catalog Number | 7451015ES |
Lot Number | SP18C211296528 |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BAXTER HEALTHCARE - SAINT PAUL |
Manufacturer Address | SAINT PAUL MN |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-10-30 |