Reported Sep 25, 2013 · Terminated
C2244.3820;, CONELOG Titanium Base CC ¿3.8GH2.0 inkl HS Product Usage: Endosseous dental implant abutment CONELOG…
Camlog USA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Camlog Usa · 5315 W 74th St Ste 200 · Indianapolis, IN · 46268-5136
Is this the product you have?
C2244.3820CONELOG Titanium Base CC ¿3.8GH2.0
- inkl HS Product UsageEndosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch
- Lot codes and dates
- 39437
- Amount recalled
- 1 in USA
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
Product not cleared for sale/use in the United States.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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