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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66143

4 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
August 28, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Camlog Usa

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

4 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 4

C2244.3808, CONELOG Titanium Base CC ¿3.8GH0.8 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.

Z-2203-2013
Recall number
Z-2203-2013
Initiated
August 28, 2013
Classification
Class II
Status
Terminated
Recalling firm
Camlog Usa
Quantity
2 in USA

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product not cleared for sale/use in the United States.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product not cleared for sale/use in the United States.

Code information

43746

Distribution pattern

USA Distribution in the states of NH, MD, CO, and IL.

device · product 2 of 4

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.

Z-2204-2013
Recall number
Z-2204-2013
Initiated
August 28, 2013
Classification
Class II
Status
Terminated
Recalling firm
Camlog Usa
Quantity
1 in USA

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product not cleared for sale/use in the United States.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product not cleared for sale/use in the United States.

Code information

39437

Distribution pattern

USA Distribution in the states of NH, MD, CO, and IL.

device · product 3 of 4

C2244.4308 CONELOG Titanium Base CC ¿4.3GH2 0.8 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.

Z-2205-2013
Recall number
Z-2205-2013
Initiated
August 28, 2013
Classification
Class II
Status
Terminated
Recalling firm
Camlog Usa
Quantity
6 to US customers

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product not cleared for sale/use in the United States.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product not cleared for sale/use in the United States.

Code information

4460 and 44163

Distribution pattern

USA Distribution in the states of NH, MD, CO, and IL.

device · product 4 of 4

C2244.5008 CONELOG Titanbasis CAD/CAM Conelog Titanium Base CAD/CAM Rx only ¿5.0GH 0.8 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.

Z-2206-2013
Recall number
Z-2206-2013
Initiated
August 28, 2013
Classification
Class II
Status
Terminated
Recalling firm
Camlog Usa
Quantity
3 in USA

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product not cleared for sale/use in the United States.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product not cleared for sale/use in the United States.

Code information

lot 43377

Distribution pattern

USA Distribution in the states of NH, MD, CO, and IL.