MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2005-04-12 for FISCHER FUTURA 3000SV * manufactured by Fischer Industries, Inc..
[20931035]
Processor is less than a year old and inconsistent. Most film is unreadable. Films have water marks, roller marks, fading and dark film. Mfr is coming to evaluate machine.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1035197 |
| MDR Report Key | 592179 |
| Date Received | 2005-04-12 |
| Date of Report | 2005-04-12 |
| Date Added to Maude | 2005-04-19 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| 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 | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | FISCHER FUTURA 3000SV |
| Generic Name | X-RAY FILM PROCESSOR |
| Product Code | IXW |
| Date Received | 2005-04-12 |
| Model Number | FUTURA 3000SV |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 582023 |
| Manufacturer | FISCHER INDUSTRIES, INC. |
| Manufacturer Address | 2630 KANEVILLE COURT GENEVA IL 60134 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2005-04-12 |