MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-12-06 for ADVIA CENTAUR XP TOXOPLASMA G (TOXO G) N/A 10310321 manufactured by Siemens Healthcare Diagnostics, Inc..
Report Number | 1219913-2019-00267 |
MDR Report Key | 9432164 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2019-12-06 |
Date of Report | 2020-03-03 |
Date of Event | 2019-02-07 |
Date Mfgr Received | 2020-02-26 |
Device Manufacturer Date | 2018-08-21 |
Date Added to Maude | 2019-12-06 |
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 | MS. STACY LOUKOS |
Manufacturer Street | 333 CONEY STREET |
Manufacturer City | EAST WALPOLE MA 02032 |
Manufacturer Country | US |
Manufacturer Postal | 02032 |
Manufacturer Phone | 5086608576 |
Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS, INC. |
Manufacturer Street | 333 CONEY STREET |
Manufacturer City | EAST WALPOLE MA 02032 |
Manufacturer Country | US |
Manufacturer Postal Code | 02032 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ADVIA CENTAUR XP TOXOPLASMA G (TOXO G) |
Generic Name | TOXOPLASMA GONDII IMMUNOASSAY, |
Product Code | LGD |
Date Received | 2019-12-06 |
Model Number | N/A |
Catalog Number | 10310321 |
Lot Number | 05337238 |
Device Expiration Date | 2019-08-21 |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS, INC. |
Manufacturer Address | 511 BENEDICT AVENUE TARRYTOWN NY 105915097 US 105915097 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-12-06 |