MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-11-19 for ORTHO VISION MAX 6904576 manufactured by Ortho Clinical Diagnostics.
| Report Number | 2250051-2019-00056 |
| MDR Report Key | 9342329 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2019-11-19 |
| Date of Report | 2019-11-19 |
| Date of Event | 2019-11-01 |
| Date Mfgr Received | 2019-11-04 |
| Date Added to Maude | 2019-11-19 |
| 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 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. JAMES A STEVENS |
| Manufacturer Street | 1001 ROUTE 202 |
| Manufacturer City | RARITAN NJ 08869 |
| Manufacturer Country | US |
| Manufacturer Postal | 08869 |
| Manufacturer Phone | 9082188223 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ORTHO VISION MAX |
| Generic Name | AUTOMATED BLOOD GROUPING & ANTIBODY TEST SYSTEM |
| Product Code | KSZ |
| Date Received | 2019-11-19 |
| Catalog Number | 6904576 |
| Lot Number | 10758750012824 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ORTHO CLINICAL DIAGNOSTICS |
| Manufacturer Address | 1001 ROUTE 202 RARITAN NJ 08869 US 08869 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-11-19 |