FDA Adverse Event
Injury
Summary report: N
SALTO TALARIS
MDR report key: 3133944
·
Received May 23, 2013
Report
- Report Number
- 9610667-2013-00151
- Event Type
- Injury
- Date Received
- May 23, 2013
- Report Date
- March 26, 2013
- Manufacturer
- TORNIER SAS
- Product Code
- HSN
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
THIS IS THE INITIAL REPORT SUBMITTED REGARDING THIS SURGICAL EVENT AND MEDICAL DEVICE.
Description of Event or Problem · 1
INFECTION
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 229702 | SALTO TALARIS | NONE | HSN | TORNIER SAS |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |