MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2006-10-11 for DAMON UTILITY OPENING/CLOSING PLIER 866-4007 manufactured by Ormco Corp..
[614491]
In 2006, a doctor informed ormco corporation that a damon opening/closing plier had a broken tip insert, braze failure.
Patient Sequence No: 1, Text Type: D, B5
[7959178]
There were no reported injuries associated with this incident. However, due to the prior submission of the reportable incident on the damon plier in 2005, (mdr #2016150-2006-00001: malfunction which led to a serious injury), this incident is reportable. This incident falls under the fda presumption that this type of malfunction is likely to cause or contribute to a death or serious injury if the malfunction were to recur.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 2016150-2006-00065 |
MDR Report Key | 854606 |
Report Source | 05 |
Date Received | 2006-10-11 |
Date of Report | 2006-09-29 |
Date of Event | 2006-09-01 |
Date Mfgr Received | 2006-09-29 |
Device Manufacturer Date | 2004-04-01 |
Date Added to Maude | 2007-05-24 |
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 | 3 |
Event Location | 0 |
Manufacturer Contact | WENDY URTEL |
Manufacturer Street | 100 BAYVIEW CIRCLE SUITE 6000 |
Manufacturer City | NEWPORT BEACH CA 92660 |
Manufacturer Country | US |
Manufacturer Postal | 92660 |
Manufacturer Phone | 9492558767 |
Manufacturer G1 | ORMCO CORPORATION |
Manufacturer Street | 1332 SOUTH LONE HILL AVENUE |
Manufacturer City | GLENDORA CA 91740 |
Manufacturer Country | US |
Manufacturer Postal Code | 91740 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DAMON UTILITY OPENING/CLOSING PLIER |
Generic Name | PLIER, ORTHODONTIC |
Product Code | JEX |
Date Received | 2006-10-11 |
Returned To Mfg | 2006-09-29 |
Model Number | NA |
Catalog Number | 866-4007 |
Lot Number | 04K45K |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 840140 |
Manufacturer | ORMCO CORP. |
Manufacturer Address | 1332 SOUTH LONE HILL AVE. GLENDORA CA 91740 US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2006-10-11 |