Z-0313-2007

Solara Replacement Turbine, Autochuck End Cap, for dental handpiece, part number 064900

Name: Z-0313-2007 Solara Replacement Turbine, Autochuck End Cap, for dental handpiece, part number 064900
Creator: Stardental Division
Published: 2006-12-01
License: https://open.fda.gov/license/

Dentalez, Inc., Stardental Division / initiated 2006-12-01 / Terminated

FDA source

Stardental Division began a recall of Solara Replacement Turbine, Autochuck End Cap, for dental handpiece, part number 064900 on 2006-12-01. The reason FDA records is "End cap component can disassemble". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0313-2007
Status: Terminated
Initiated: 2006-12-01
Posted: 2006-12-27
Terminated: 2007-06-12
Recalling firm: Dentalez, Inc., Stardental Division
Product: Solara Replacement Turbine, Autochuck End Cap, for dental handpiece, part number 064900.
Product code: EFA Handpiece, Belt And/Or Gear Driven, Dental
Reason for recall: End cap component can disassemble.
FDA root cause: Other
Action: The recalling firm sent recall letters to dealers and doctors via certified mail, return receipt on 12/6/06. Letters to the foreign accounts were sent via UPS or other traceable methods.
Quantity in commerce: 2756 end caps
Distribution: Worldwide distribution, including USA, Canada and Japan.
Product codes and lots: Part number 064900, Lot numbers 1694789, 1697998, 1699566, and 1703516.0

Product code EFA

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)