MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-08-03 for DETECTO STADIOMETER SCALE 439 manufactured by Cardinal Scale Mfg. Co..
[51021395]
Patient Sequence No: 1, Text Type: N, H10
[51021396]
The patient used the stadiometer rod to stabilize herself. The stadiometer rod was not lowered to its lowest position. The top of the rod has a metal plate that does have a sharp edge. As the patient was reaching for the stadiometer to stabilize herself she grabbed this portion of the rod and came into contact with the sharp edge. Cautery required to stop bleeding.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 5842686 |
| MDR Report Key | 5842686 |
| Date Received | 2016-08-03 |
| Date of Report | 2016-07-25 |
| Date of Event | 2016-07-15 |
| Report Date | 2016-07-25 |
| Date Reported to FDA | 2016-07-25 |
| Date Reported to Mfgr | 2016-07-25 |
| Date Added to Maude | 2016-08-03 |
| 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 |
| 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 | 3 |
| Brand Name | DETECTO STADIOMETER SCALE |
| Generic Name | SCALE |
| Product Code | MNW |
| Date Received | 2016-08-03 |
| Model Number | 439 |
| Device Availability | * |
| Device Age | 8 YR |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CARDINAL SCALE MFG. CO. |
| Manufacturer Address | 203 EAST DAUGHERTY WEBB CITY MO 64870 US 64870 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other; 2. Required No Informationntervention | 2016-08-03 |