MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-09-11 for RITTER 222 manufactured by Ritter / Midmark.
[85798728]
Constantly having to order new power control board (pcb) from the mfr to repair the new equipment being used in the clinics. Mfr: ritter, model: 222 nomenclature: exam table. I am a medical maintenance tech currently stationed in (b)(6) and these boards are going out and the mfr is making us pay for them which cost us $(b)(6) a board. One board per exam table and they are going to slowly die and the mfr just tells us we will need to order the upgraded pcb that will work properly. We currently maintain 36 of these models all over our (b)(6) footprint. Thanks (b)(6).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5072070 |
| MDR Report Key | 6854425 |
| Date Received | 2017-09-11 |
| Date of Report | 2017-09-07 |
| Date of Event | 2017-09-07 |
| Date Added to Maude | 2017-09-11 |
| 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 | MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | RITTER 222 |
| Generic Name | EXAMINATION TABLE, AC POWERED |
| Product Code | LGX |
| Date Received | 2017-09-11 |
| Model Number | 222 |
| Device Expiration Date | 2017-09-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | RITTER / MIDMARK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-09-11 |