FDA Adverse Event
Other
Summary report: N
DISP DERMAL CURETTES 4MM
MDR report key: 1553155
·
Received November 7, 2009
Report
- Report Number
- 2523190-2009-00003
- Event Type
- Other
- Date Received
- November 7, 2009
- Report Date
- December 7, 2009
- Product Code
- JYG
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VT, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
TO DATE, THE DEVICE INVOLVED IN THE REPORTED INCIDENT HAS NOT BEEN RECEIVED FOR EVALUATION. AN INVESTIGATION HAS BEEN INITIATED BASED ON THE REPORTED INFORMATION.
Description of Event or Problem · 1
A REGISTERED NURSE WAS REMOVING INDIVIDUAL PACKAGES OF STERILE DISPOSABLE CURETTES FROM THE BOX. WHILE REMOVING THE PRODUCTS, SHE CUT HER RIGHT INDEX FINGER ON A CURETTE, REQUIRING 4 STITCHES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DISP DERMAL CURETTES 4MM | M3 - DERMAL | JYG | 081006 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |