MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-12-13 for CAPTUS 3000 UPTAKE PROBE manufactured by Capintec. Inc..
[17159678]
The tech in nuclear medicine was positioning the uptake probe to take a count during a thyroid scan. The probe was over the pt's leg when the probe fell on the pt's left knee. The pt stated she had 6/10 left knee after the incident. The pt was able to walk and bear weight afterwards. Ice was provided immediately and the pt was taken to the ed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5033476 |
| MDR Report Key | 3525152 |
| Date Received | 2013-12-13 |
| Date of Report | 2013-12-12 |
| Date of Event | 2013-12-11 |
| Date Added to Maude | 2013-12-19 |
| 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 | CAPTUS 3000 UPTAKE PROBE |
| Generic Name | CAPTUS |
| Product Code | IZD |
| Date Received | 2013-12-13 |
| Operator | HEALTH PROFESSIONAL |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CAPINTEC. INC. |
| Manufacturer Address | US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2013-12-13 |