Z-0452-06

PlusRite Universal Metal Halide Lamps

Name: Z-0452-06 PlusRite Universal Metal Halide Lamps
Creator: Fanlight Corporation Inc
Published: 2006-03-24
License: https://open.fda.gov/license/

Fanlight Corporation Inc / initiated 2006-03-24 / Terminated

FDA source

Fanlight Corporation Inc began a recall of PlusRite Universal Metal Halide Lamps on 2006-03-24. The reason FDA records is "These non-self-extinguishing mercury vapor and metal halide lamps failed to comply with the performance requirements of 21 CFR 1040.30 and the certification and identification requirements of 21 CFR 1010.2 and 1010.3". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0452-06
Status: Terminated
Initiated: 2006-03-24
Posted: 2006-06-08
Terminated: 2008-01-22
Recalling firm: Fanlight Corporation Inc
Product: PlusRite Universal Metal Halide Lamps
Product code: U28
Reason for recall: These non-self-extinguishing mercury vapor and metal halide lamps failed to comply with the performance requirements of 21 CFR 1040.30 and the certification and identification requirements of 21 CFR 1010.2 and 1010.3
FDA root cause: Other
Action: 1.Fanlight Corporation, Incorporated shall notify all dealers and purchasers requesting that the recipients forward a copy of the letter on to each recipient''s customers, with the objective of notifying as many end users as possible. Fanlight at no cost to the purchaser will bring the units into compliance
Quantity in commerce: 100,000 total for all 5 products
Distribution: Nationwide
Product codes and lots: N/A

Product code U28

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)