MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-04-26 for EXODONTIA ELEVATOR #46R, SERRATED N/A 09-0252 manufactured by Biomet Microfixation.
[145276742]
(b)(4). Product has been received by zimmer biomet and the investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10
[145276743]
It was reported that the instrument fractured at the tip during a tooth extraction. The fractured piece was suctioned from the patients mouth. No adverse events have been reported as a result of the malfunction.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 0001032347-2019-00254 |
MDR Report Key | 8558265 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-04-26 |
Date of Report | 2019-05-31 |
Date of Event | 2019-03-26 |
Date Mfgr Received | 2019-05-06 |
Device Manufacturer Date | 2018-01-05 |
Date Added to Maude | 2019-04-26 |
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 | DENTIST |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MRS. MERRIANNE CASSIDY |
Manufacturer Street | 1520 TRADEPORT DRIVE |
Manufacturer City | JACKSONVILLE FL 32218 |
Manufacturer Country | US |
Manufacturer Postal | 32218 |
Manufacturer Phone | 9047414400 |
Manufacturer G1 | BIOMET MICROFIXATION |
Manufacturer Street | 1520 TRADEPORT DRIVE |
Manufacturer City | JACKSONVILLE FL 32218 |
Manufacturer Country | US |
Manufacturer Postal Code | 32218 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | N/A |
Event Type | 3 |
Type of Report | 3 |
Brand Name | EXODONTIA ELEVATOR #46R, SERRATED |
Generic Name | ELEVATOR, SURGICAL, DENTAL |
Product Code | EMJ |
Date Received | 2019-04-26 |
Returned To Mfg | 2019-04-26 |
Model Number | N/A |
Catalog Number | 09-0252 |
Lot Number | 121217K17 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOMET MICROFIXATION |
Manufacturer Address | 1520 TRADEPORT DRIVE JACKSONVILLE FL 32218 US 32218 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-04-26 |