MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1995-05-17 for RECLINER BLUE 9900077 manufactured by Lumex.
[15378208]
Facility alleges pt fell from chair and hit back of head. Staff states that this chair is unable to keep balance with pts on it; if pt raises or crosses his legs while in the reading position, it will tilt back along with pt. Pt stated he was fine. No injury revealed on x-rays.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2243621-1995-00491 |
| MDR Report Key | 22287 |
| Date Received | 1995-05-17 |
| Date of Report | 1995-05-10 |
| Date of Event | 1995-04-25 |
| Date Facility Aware | 1995-05-04 |
| Report Date | 1995-05-10 |
| Date Reported to FDA | 1995-05-10 |
| Date Reported to Mfgr | 1995-05-10 |
| Date Added to Maude | 1995-06-08 |
| Event Key | 0 |
| Report Source Code | Distributor 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 | RECLINER BLUE |
| Generic Name | RECLINER BLUE |
| Product Code | FIA |
| Date Received | 1995-05-17 |
| Catalog Number | 9900077 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | * |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 22404 |
| Manufacturer | LUMEX |
| Manufacturer Address | BAYSHORE NY 11706 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 1995-05-17 |