MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2012-05-04 for ADVIA CENTAUR CORTISOL (COR) ASSAY N/A 04610138 manufactured by Siemens Healthcare Diagnostics, Inc..
[2753912]
The customer reported that they did not receive a advia centaur cortisol urgent field safety notice (b)(4) that was distributed to customers in march 2012. There was no report of adverse health consequences.
Patient Sequence No: 1, Text Type: D, B5
[9836888]
Urgent field safety notice ((b)(4)) was provided to the customer.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1219913-2012-00186 |
MDR Report Key | 2559394 |
Report Source | 05,06 |
Date Received | 2012-05-04 |
Date of Report | 2012-04-06 |
Date of Event | 2012-03-07 |
Date Mfgr Received | 2012-04-06 |
Date Added to Maude | 2012-09-19 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | MR. STEPHEN PERRY |
Manufacturer Street | 333 CONEY ST. |
Manufacturer City | EAST WALPOLE MA 02032 |
Manufacturer Country | US |
Manufacturer Postal | 02032 |
Manufacturer Phone | 5086604163 |
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 |
Remedial Action | NO |
Previous Use Code | 3 |
Removal Correction Number | Z-1390-2012 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ADVIA CENTAUR CORTISOL (COR) ASSAY |
Generic Name | CORTISOL IMMUNOASSAY |
Product Code | JFT |
Date Received | 2012-05-04 |
Model Number | N/A |
Catalog Number | 04610138 |
Lot Number | 257 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS, INC. |
Manufacturer Address | TARRYTOWN NY 10591 US 10591 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2012-05-04 |