FDA Medical Device Recalls (openFDA)
Fanlight Corporation Inc: PlusRite Power Strike Metal Halide Lamps
- Recall number
- Z-0450-06
- Recalling firm
- Fanlight Corporation Inc
- Product
- PlusRite Power Strike Metal Halide Lamps
- Status
- Terminated
- Initiated
- 2006-03-24
- Posted
- 2006-06-08
- Terminated
- 2008-01-22
- Reason
- 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
- 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
- 100,000 total for all 5 products
- Distribution
- Nationwide
- Lot, serial or model codes
- n/a
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- U28
- Firm FEI
- 3005191388
- Firm city
- City Of Industry
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28