MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-17 for SIR SHPERES Y-90 MICROSPHERES SIR-Y001 manufactured by Sirtex Wilmington Llc.
Report Number | 3005579300-2019-00004 |
MDR Report Key | 8704224 |
Date Received | 2019-06-17 |
Date of Report | 2019-06-17 |
Date of Event | 2019-04-04 |
Date Mfgr Received | 2019-06-12 |
Date Added to Maude | 2019-06-17 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | STEPHANIE WHITNELL |
Manufacturer Street | 300 UNICORN PARK DR. |
Manufacturer City | WOBURN MA 01801 |
Manufacturer Country | US |
Manufacturer Postal | 01801 |
Manufacturer Phone | 8884747839 |
Manufacturer G1 | SIRTEX WILMINGTON LLC |
Manufacturer Street | 16 UPTON DR. NO. 2-4 |
Manufacturer City | WILMINGTON MA 01887 |
Manufacturer Country | US |
Manufacturer Postal Code | 01887 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | SIR SHPERES Y-90 MICROSPHERES |
Generic Name | YTTRIUM-90 RESIN MICROSPHERES |
Product Code | NAW |
Date Received | 2019-06-17 |
Model Number | SIR-Y001 |
Catalog Number | SIR-Y001 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIRTEX WILMINGTON LLC |
Manufacturer Address | 16 UPTON DR. NO. 2-4 WILMINGTON MA 01887 US 01887 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-06-17 |