FDA Adverse Event
Malfunction
Summary report: N
3.5MM RESECTOR CUTTER, FORMULA (5BX)
MDR report key: 2870532
·
Received November 14, 2012
Report
- Report Number
- 2648666-2012-00357
- Event Type
- Malfunction
- Date Received
- November 14, 2012
- Date of Event
- October 17, 2012
- Report Date
- October 18, 2012
- Manufacturer
- STRYKER ENDOSCOPY PUERTO RICO
- Product Code
- HRX
- PMA / PMN Number
- K941333
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AS
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
ADD'L INFO WILL BE PROVIDED ONCE THE INVESTIGATION HAS BEEN COMPLETED.
Description of Event or Problem · 1
IT WAS REPORTED THAT DURING AN ARTHROSCOPY PROCEDURE, THE BLADE UNIT BROKE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 3.5MM RESECTOR CUTTER, FORMULA (5BX) | HRX | STRYKER ENDOSCOPY PUERTO RICO | 12212CE2 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |