C2244 — Class II medical device recall Z-2204-2013
Terminated recall by Camlog Usa, reported 2013-09-25, distributed in CO, IL, MD, NH. Product not cleared for sale/use in the United States.
| Recall number | Z-2204-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Camlog Usa, Indianapolis, IN, United States |
| Recall initiated | 2013-08-28 |
| Classified | 2013-09-16 |
| Reported by FDA | 2013-09-25 |
| Terminated | 2014-01-29 |
| Distributed | CO, IL, MD, NH |
| Quantity | 1 in |
| Reason classes | unapproved 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 mandibular arch.
Reason for recall
Product not cleared for sale/use in the United States.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2204-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.