Camlog USA Recalls Uncleared Dental Implant Abutments in Four States
Camlog USA is recalling one unit of a CONELOG Titanium Base dental implant abutment because it was not cleared for sale or use in the United States.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity level. The hazard is a regulatory compliance issue (product not cleared for sale) rather than a direct physical injury or contamination risk, and no illnesses or injuries are reported in the source text.
Plain-English summary
Camlog USA is recalling one unit of the CONELOG Titanium Base CC 3.8GH2.0 inkl HS dental implant abutment (Product Code C2244.3820). The recall is being conducted because the product was not cleared for sale or use in the United States.
The affected unit was distributed in the United States to the states of New Hampshire, Maryland, Colorado, and Illinois. The specific code associated with the recalled item is 39437.
Consumers who possess this specific dental implant abutment should stop using it and contact Camlog USA for further instructions. This recall addresses a regulatory compliance issue regarding the product's clearance status in the US market.
The recalled product
- Product
- C2244.3820;, CONELOG Titanium Base CC ¿3.8GH2.0 inkl HS Product Usage: Endosseous 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 mandibul
- Manufacturer
- Camlog Usa
- Affected units
- 1
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- 39437
Distribution
Part of a larger recall action
This product is one of 4 recalled by Camlog Usa under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 4 products in this recall →Related recalls
Same manufacturer · Camlog Usa
See all →- ModerateCamlog Dental Implant Abutments Recalled for Lack of FDA Clearance
FDA (Devices) · 2013-09-25
- ModerateCamlog USA Recalls Uncleared Dental Implant Abutments in Four States
FDA (Devices) · 2013-09-25
- ModerateCamlog USA Recalls Uncleared Dental Implant Abutments
FDA (Devices) · 2013-09-25
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