FDA Adverse Event
Injury
Summary report: N
DESARA
MDR report key: 4201087
·
Received October 20, 2014
Report
- Report Number
- 3003990090-2014-00036
- Event Type
- Injury
- Date Received
- October 20, 2014
- Date of Event
- July 2, 2010
- Report Date
- September 24, 2014
- Manufacturer
- CALDERA MEDICAL, INC.
- Product Code
- OTN
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
EVENT WAS REPORTED TO CALDERA MEDICAL BY AN ATTORNEY. LEGAL COMPLAINT STATES THAT THE PATIENT SUFFERED INJURIES AND DAMAGES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 667124 | DESARA | SURGICAL MESH | OTN | CALDERA MEDICAL, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |