MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2011-11-15 for ASPARTATE AMINOTRANSFERASE PYRIDOXAL-5'-PHOSPHASE REAGENT 467845 manufactured by Beckman Coulter, Inc..
[20915458]
International customer reported that the synchron aspartate aminotransferase pyridoxal-5'-phosphase (ast) reagent cartridge leaked. No injuries were reported.
Patient Sequence No: 1, Text Type: D, B5
[21145131]
No product was returned for evaluation, accordingly, no conclusion can be drawn. This reportable event was identified during a retrospective review of complaints conducted between january 1, 2008 and october 23, 2010 for additional reportable events.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2050012-2011-07388 |
| MDR Report Key | 2393378 |
| Report Source | 01,05,06 |
| Date Received | 2011-11-15 |
| Date of Report | 2010-07-12 |
| Date of Event | 2010-05-21 |
| Date Mfgr Received | 2010-07-12 |
| Date Added to Maude | 2012-07-16 |
| 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 | MS NORA ZEROUNIAN |
| Manufacturer Street | 250 SOUTH KRAEMER BLVD. |
| Manufacturer City | BREA CA 92821 |
| Manufacturer Country | US |
| Manufacturer Postal | 92821 |
| Manufacturer Phone | 7149613634 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ASPARTATE AMINOTRANSFERASE PYRIDOXAL-5'-PHOSPHASE REAGENT |
| Product Code | CIT |
| Date Received | 2011-11-15 |
| Model Number | NA |
| Catalog Number | 467845 |
| Lot Number | UNK |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BECKMAN COULTER, INC. |
| Manufacturer Address | 250 SOUTH KRAEMER BLVD. BREA CA 92821 US 92821 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2011-11-15 |