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 |