MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a * report with the FDA on 2012-08-16 for DAILY ACTIVITY ASSIST DEVICES 6895 manufactured by Kenstone Metal.
[2793835]
Dealer called stating that the seat on the 6895 shower commode chair allegedly broke. Replacement seat has been ordered. No injury alleged. Mdr filed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1531186-2012-00718 |
| MDR Report Key | 2701331 |
| Report Source | * |
| Date Received | 2012-08-16 |
| Date of Report | 2012-08-15 |
| Date Facility Aware | 2012-07-18 |
| Report Date | 2012-08-15 |
| Date Reported to FDA | 2012-08-15 |
| Date Reported to Mfgr | 2012-08-15 |
| Date Added to Maude | 2012-12-04 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| 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 | 0 |
| Single Use | 0 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DAILY ACTIVITY ASSIST DEVICES |
| Generic Name | 890.5050 |
| Product Code | INB |
| Date Received | 2012-08-16 |
| Model Number | 6895 |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | KENSTONE METAL |
| Manufacturer Address | KUNSHAN CH |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2012-08-16 |