MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 99 report with the FDA on 2006-05-17 for NONE manufactured by .
[1069379]
Participant pulled his right calf muscle. He was given naproxen to take twice a day as needed. The participant has been using heat and ice to treat. This resolved in a two week time frame. See scanned page.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1357818 |
| MDR Report Key | 1357818 |
| Report Source | 99 |
| Date Received | 2006-05-17 |
| Date of Report | 2006-05-16 |
| Date of Event | 2006-04-14 |
| Date Facility Aware | 2006-04-17 |
| Report Date | 2006-05-16 |
| Date Reported to FDA | 2006-05-16 |
| Date Added to Maude | 2009-04-14 |
| 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 | 0 |
| 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 | NA |
| Generic Name | NONE |
| Product Code | ITH |
| Date Received | 2006-05-17 |
| Device Age | 3 YR |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2006-05-17 |