FDA Adverse Event
Malfunction
Summary report: N
4MM DIAMOND BALL
MDR report key: 3140711
·
Received May 31, 2013
Report
- Report Number
- 1045834-2013-02243
- Event Type
- Malfunction
- Date Received
- May 31, 2013
- Date of Event
- February 28, 2013
- Report Date
- February 28, 2013
- Manufacturer
- DEPUY SNYTHES POWER TOOLS
- Product Code
- HBC
- PMA / PMN Number
- K011444
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE CUTTER/BURR DEVICE WAS NOT RECEIVED FOR EVALUATION. THEREFORE, THE REPORTED CONDITION WAS NOT CONFIRMED. IF ADDITIONAL INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SENT. (B)(4).
Description of Event or Problem · 1
REPORT RECEIVED FROM (B)(6) REGARDING A CUTTER/BURR DEVICE IN WHICH THE "STERILE PACK WAS DEFORMED". THE ALLEGED DEFECT WAS OBSERVED UPON RECEIPT OF THE PRODUCT, DURING INSPECTION. THEREFORE, THE DEVICE WAS NOT USED IN SURGERY. NO INJURIES OR MEDICAL INTERVENTION WERE REPORTED. NO ADDITIONAL INFORMATION WAS AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 241903 | 4MM DIAMOND BALL | MOTOR, DRILL, ELECTRIC-CUTTER | HBC | DEPUY SNYTHES POWER TOOLS | F476012160 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |