MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,08 report with the FDA on 2012-03-15 for MIRROR - DBL SIDED, SZ 5 67723 manufactured by Integra York, Pa Inc..
[18280345]
"mirrors separating from frame. " on (b)(6) 2012 the dental hygienist reported that 2 of these mirrors has fallen out of the frame while inside a patient's mouth. No injury was reported.
Patient Sequence No: 1, Text Type: D, B5
[18521863]
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.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 2523190-2012-00026 |
MDR Report Key | 2498354 |
Report Source | 05,06,08 |
Date Received | 2012-03-15 |
Date of Report | 2012-03-15 |
Date Mfgr Received | 2012-03-05 |
Date Added to Maude | 2012-08-29 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | CAREN FERNANDEZ |
Manufacturer Street | 315 ENTERPRISE DR. |
Manufacturer City | PLAINSBORO NJ 08536 |
Manufacturer Country | US |
Manufacturer Postal | 08536 |
Manufacturer Phone | 6099362341 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MIRROR - DBL SIDED, SZ 5 |
Generic Name | M52 - HYGIENE / PERIODONTAL |
Product Code | EAX |
Date Received | 2012-03-15 |
Catalog Number | 67723 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INTEGRA YORK, PA INC. |
Manufacturer Address | YORK PA 17402 US 17402 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2012-03-15 |