Z-1077-2007

DCI Equipment Track Mount Light Assembly, 110v

Name: Z-1077-2007 DCI Equipment Track Mount Light Assembly, 110v
Creator: Dental Equipment LLC
Published: 2007-05-01
License: https://open.fda.gov/license/

DCI International, LLC / initiated 2007-05-01 / Terminated

FDA source

Dental Equipment LLC began a recall of DCI Equipment Track Mount Light Assembly, 110v on 2007-05-01. The reason FDA records is "Potential for light shield to melt due to light assemblies not properly rated to handle the VAC". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1077-2007
Status: Terminated
Initiated: 2007-05-01
Posted: 2007-07-12
Terminated: 2007-07-12
Recalling firm: DCI International, LLC
Product: DCI Equipment Track Mount Light Assembly, 110v
Product code: EAZ Light, Operating, Dental
Reason for recall: Potential for light shield to melt due to light assemblies not properly rated to handle the VAC.
FDA root cause: Other
Action: On 5/1/07 the dental office contacted the manufacturer via telephone regarding the incident. On 5/2/07 the firm's service representative visited the dental office and replaced the lights.
Quantity in commerce: 4 dual track lights
Distribution: The lights were distributed to one distributor in NY who in turn distributed the lights to one dental office.
Product codes and lots: All products of this type. Product does not contain serial numbers or any other identifying codes.

Product code EAZ

The FDA recall record names no cleared device, and no clearance has been matched to it.

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)