FDA Adverse Event
Malfunction
Summary report: N
NITE GUARD
MDR report key: 4113771
·
Received May 1, 2014
Report
- Report Number
- 1825660-2014-00071
- Event Type
- Malfunction
- Date Received
- May 1, 2014
- Date of Event
- January 22, 2013
- Report Date
- April 29, 2014
- Manufacturer
- RANIR, LLC
- Product Code
- OBR
- PMA / PMN Number
- K120103
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
THIS COMPLAINT HAS NOT BEEN CONFIRMED. DEVICE NOT RETURNED TO MANUFACTURER, AND NO LOT NUMBER INFO WAS GIVEN SO AN EVAL CANNOT BE PERFORMED AS TO THE ROOT CAUSE OR ACTUAL NATURE OF THE PROBLEM. NO INJURY WAS REPORTED, NO MEDICAL ATTENTION WAS REPORTED TO HAVE BEEN SOUGHT. THIS IS BEING REPORTED AS A POSSIBLE DELAMINATION, AS CHOKING IS POSSIBLE AS A RESULT OF DELAMINATION.
Description of Event or Problem · 1
EXPLAINED THAT THE RUBBER MATERIAL GETS REALLY THIN IN THE FRONT WHEN YOU TRY AND SMOOTH IT OUT TO YOUR TEETH. I MADE IT TOO THIN IT DIDN'T FEEL RIGHT. ALSO, AFTER USING THE FIRST GUARD FOR LESS THAN TWO WEEKS, I HAD ALREADY GRINDED THROUGH THE RUBBER AND IT STARTED TO DETACH FROM THE BLUE SURFACE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 262594 | NITE GUARD | OBR | RANIR, LLC | GEN III |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |