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.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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…
- 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
Same hazard · regulatory non compliance
See all →- ModerateLimitless Cryo Spa LLC Recalls Glypto Devices for Lack of 510(k) Clearance
FDA (Devices) · 2026-10-14
- SevereSempio Recalls Ready-to-Eat Chicken Stew Imported Without Reinspection
USDA FSIS · 2026-09-25
- ModerateMedline Polycarbonate Syringes Recalled for Unapproved Design Changes
FDA (Devices) · 2026-07-01
- SevereMedline polycarbonate syringes recalled for unapproved design changes
FDA (Devices) · 2026-07-01
- ModerateMedline 10mL Polycarbonate Syringes Recalled for Unapproved Design Changes
FDA (Devices) · 2026-07-01
Similar recalls
- ModerateUnapproved Dental Implants Recalled by Instradent USA
FDA (Devices) · 2014-12-31
- ModerateKeystone Dental Recalls Multi-Unit Abutments Due to Screw Fit Issues
FDA (Devices) · 2018-02-21
- ModerateNobel Biocare Recalls Dental Implant Healing Abutments Due to Sizing Error
FDA (Devices) · 2020-06-10
- HighDental abutment recall due to incorrect product packaging and labeling
FDA (Devices) · 2024-07-17
- ModerateBiomet 3i Recalls Titanium Dental Abutments Due to Manufacturing Defect
FDA (Devices) · 2019-08-14
- ModerateDental Abutments Recalled for Incorrect Version Identification Stickers
FDA (Devices) · 2025-03-12