FDA Adverse Event
Injury
Summary report: N
PAIN CARE 3200
MDR report key: 2142310
·
Received June 20, 2011
Report
- Report Number
- 2028253-2011-00040
- Event Type
- Injury
- Date Received
- June 20, 2011
- Date of Event
- May 20, 2004
- Report Date
- June 17, 2011
- Manufacturer
- BREG, INC.
- Product Code
- FRN
- PMA / PMN Number
- K013928
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
BREG RECEIVED LEGAL NOTICE OF FILED LAWSUIT WITH USE OF PAIN CARE 3200. PATIENT HAD SHOULDER SURGERY AND ALLEGES CHONDROLYSIS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PAIN CARE 3200 | 88 FRN | FRN | BREG, INC. | PAIN CARE | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other| S |