MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2015-01-08 for 3I INCISE ZR COPING SHADE 2 N/A CBZR0102 manufactured by Biomet 3i.
[5309635]
The doctor reported that the zirconia coping fractured into fragments.
Patient Sequence No: 1, Text Type: D, B5
[12656865]
Product has not been returned to manufacturer.
Patient Sequence No: 1, Text Type: N, H10
[12900867]
(b)(4). The coping was discarded and not returned by the customer. The complaint could not be verified. Dhr did not indicate any manufacturing deviations that would contribute to this event. A definitive root cause could not be determined. There were no manufacturing deviations which may have contributed to the reported fracture.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 0001038806-2014-00187 |
MDR Report Key | 4397894 |
Report Source | 05 |
Date Received | 2015-01-08 |
Date of Report | 2014-12-16 |
Date Mfgr Received | 2015-01-16 |
Device Manufacturer Date | 2014-05-15 |
Date Added to Maude | 2015-01-27 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | MS. DANIA PEREZ |
Manufacturer Street | 4555 RIVERSIDE DRIVE |
Manufacturer City | PALM BEACH GARDENS FL 33410 |
Manufacturer Country | US |
Manufacturer Postal | 33410 |
Manufacturer Phone | 5617766700 |
Manufacturer G1 | BIOMET 3I |
Manufacturer Street | 4555 RIVERSIDE DRIVE |
Manufacturer City | PALM BEACH GARDENS FL 33410 |
Manufacturer Country | US |
Manufacturer Postal Code | 33410 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | N/A |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 3I INCISE ZR COPING SHADE 2 |
Generic Name | ZIRCONIA COPING |
Product Code | NSP |
Date Received | 2015-01-08 |
Model Number | N/A |
Catalog Number | CBZR0102 |
Lot Number | 142265 |
ID Number | N/A |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOMET 3I |
Manufacturer Address | 4555 RIVERSIDE DRIVE PALM BEACH GARDENS FL 33410 US 33410 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-01-08 |