MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-08-31 for MIDMARK RITTER 308-002-202 CS061-0418-00 manufactured by Midmark Corp..
[16324355]
The exam table is hard to change the positions using the side lever. This difficulty causes the lever to strip and therefore stop working. The manager informed me that she had to have the levers replaced. Within the last year, she has had 10 tables' levers replaced.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2752430 |
| MDR Report Key | 2752430 |
| Date Received | 2012-08-31 |
| Date of Report | 2012-08-31 |
| Date of Event | 2012-08-27 |
| Report Date | 2012-08-31 |
| Date Reported to FDA | 2012-08-31 |
| Date Added to Maude | 2012-09-20 |
| 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 | 3 |
| Reporter Occupation | RISK MANAGER |
| 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 | MIDMARK RITTER |
| Generic Name | TABLE, EXAMINATION, MEDICAL, POWERED |
| Product Code | LGX |
| Date Received | 2012-08-31 |
| Model Number | 308-002-202 |
| Catalog Number | CS061-0418-00 |
| Lot Number | 025600008392 |
| ID Number | * |
| Operator | PHYSICIAN |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MIDMARK CORP. |
| Manufacturer Address | 60 VISTA DRIVE P.O. BOX 286 VERSAILLES OH 45380 US 45380 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-08-31 |