FDA Adverse Event
Malfunction
Summary report: N
TX1 TISSUE REMOVAL SYSTEM - MICROTIP
MDR report key: 3902925
·
Received February 24, 2014
Report
- Report Number
- 2085033-2014-00531
- Event Type
- Malfunction
- Date Received
- February 24, 2014
- Date of Event
- January 13, 2014
- Report Date
- February 14, 2014
- Manufacturer
- TENEX HEALTH
- Product Code
- LFL
- PMA / PMN Number
- K123640
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
UNIT PRIMED FINE, WOULD NOT CUT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 114261 | TX1 TISSUE REMOVAL SYSTEM - MICROTIP | ULTRASONIC SURGICAL ASPIRATOR | LFL | TENEX HEALTH | 14413-05 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |