MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2008-08-28 for CLINICAL CHEMISTRY AST-ACTIVATED 8L91-40 manufactured by Abbott Manufacturing, Inc..
Report Number | 2018433-2008-00181 |
MDR Report Key | 1145531 |
Report Source | 01,05 |
Date Received | 2008-08-28 |
Date of Report | 2008-05-16 |
Date of Event | 2008-05-16 |
Date Mfgr Received | 2008-12-18 |
Device Manufacturer Date | 2007-09-20 |
Date Added to Maude | 2009-04-27 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | DR. KHAUDEJA BANO |
Manufacturer Street | 100 ABBOTT PARK ROAD D09Y6, AP6C-2 |
Manufacturer City | ABBOTT PARK IL 600646112 |
Manufacturer Country | US |
Manufacturer Postal | 600646112 |
Manufacturer Phone | 8479386319 |
Manufacturer G1 | ABBOTT MANUFACTURING, INC. |
Manufacturer Street | 820 MISSION ST. |
Manufacturer City | SOUTH PASADENA CA 91030 |
Manufacturer Country | US |
Manufacturer Postal Code | 91030 |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Removal Correction Number | 2018433-08/07/08-003-C |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CLINICAL CHEMISTRY AST-ACTIVATED |
Generic Name | FOR THE QUANTITATION OF ASPARTATE AMINOTRANSFERASE IN HUMAN SERUM OR PLASMA |
Product Code | CIT |
Date Received | 2008-08-28 |
Model Number | NA |
Catalog Number | 8L91-40 |
Lot Number | 57017HW00 |
ID Number | NA |
Device Expiration Date | 2008-08-10 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ABBOTT MANUFACTURING, INC. |
Manufacturer Address | 820 MISSION ST. SOUTH PASADENA CA 91030 US 91030 |