MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1995-05-20 for CINEPROJECTOR 35AX manufactured by Tagarno.
[12412]
Cineprojector bulb exploded into physicians hair & face. No injuries were reported. Cineprojectors are used in pt room's by the physicians, with potential for pt injury. Equipment found to have shorted transistor shorting out. This was replaced by biomedical personnel.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 24823 |
| MDR Report Key | 24823 |
| Date Received | 1995-05-20 |
| Date of Report | 1995-05-12 |
| Date of Event | 1995-04-28 |
| Date Facility Aware | 1995-04-28 |
| Report Date | 1995-05-12 |
| Date Added to Maude | 1995-08-22 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | CINEPROJECTOR |
| Generic Name | PROJECTOR |
| Product Code | IZJ |
| Date Received | 1995-05-20 |
| Model Number | 35AX |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | UNKNOWN |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 27929 |
| Manufacturer | TAGARNO |
| Manufacturer Address | DOVER DE 199014644 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 1995-05-20 |