| Catalog Number |
CT3111 |
| Medical Device Problem Code |
Adverse Event Without Identified Device or Use Problem (2993)
|
| Health Effect - Clinical Codes |
Unspecified Infection (1930); Inflammation (1932)
|
| Date of Event |
05/30/2024
|
|
Type of Reportable Event
|
Serious Injury
|
|
Event or Problem Description
|
|
It was reported that the implant at tooth site #ll2 was removed due to infection.Symptoms as a result of the event: inflammation.
|
| |
|
Additional Manufacturer Narrative
|
|
Zimvie complaint number (b)(4).
|
| |
|
Event or Problem Description
|
|
No further event information is available at the time of this report.
|
| |
|
Additional Manufacturer Narrative
|
|
Zimvie complaint number (b)(4).The following fields have been updated: b4: date of this report b5: describe event or problem d9: device availability g3: date received by manufacturer g6: type of report h1: type of reportable event h2: follow up type h3: device evaluated by manufacturer h10: additional narrative dhr review was completed for the subject lot number 1220714.No deviations or non-conformances, which could have caused or contributed to the reported event, were noted as part of the dhr.Complaint history review was performed for the reported lot number 1220714 for similar events and no other complaint was identified.Review completed utilizing keywords: infection a summary investigation has been completed for infection events identifying that a definitive root cause cannot be identified due to the wide range of external (non-design/ non-manufacturing related) factors potentially impacting the sterility of the implant and its environment.Should additional information be received which indicates that the device may have caused or contributed to the infection event, an additional report will be submitted.Summary investigation.
|
| |
|
Search Alerts/Recalls
|