MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-05-18 for RITTER CHAIR RITTER 319 manufactured by .
[2639855]
A ritter chair (b)(4), model # 319-003, serial (b)(4) had the back release unexpectedly this happened twice appears that nuts loosened with repeated use.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5025472 |
| MDR Report Key | 2588366 |
| Date Received | 2012-05-18 |
| Date of Report | 2012-05-18 |
| Date Added to Maude | 2012-05-31 |
| 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 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | RITTER CHAIR |
| Generic Name | NONE |
| Product Code | ETF |
| Date Received | 2012-05-18 |
| Model Number | RITTER 319 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-05-18 |