Santajoy recalls E-Z Illuminations Galaxy Laser projectors that may emit radiation exceeding federal Class IIIa standards. Owners should stop using these devices immediately.
It was discovered that the product units it imported may, at peak levels, emit radiation that exceeds the federal standard for Class IIIa products.
Santajoy is recalling E-Z Illuminations Galaxy Laser projectors that could emit radiation levels above federal safety limits. This poses a risk of potential health effects from prolonged exposure to excessive radiation.
These projectors may emit radiation levels that exceed federal safety standards for Class IIIa products. Prolonged exposure to such radiation could potentially cause health effects, though the exact risk level is not specified in the recall.
Owners of E-Z Illuminations Galaxy Laser projectors with model numbers EZ-Illuminations Galaxy or EZ-Illuminations Northern Lights are affected. Children and individuals with radiation-sensitive health conditions may be at higher risk.
Check for model numbers EZ-Illuminations Galaxy or EZ-Illuminations Northern Lights on the product. These projectors were sold as decorative entertainment devices.
Immediately stop using the E-Z Illuminations Galaxy Laser projectors as they may emit radiation exceeding federal safety limits.
The recall states that these projectors may emit radiation exceeding federal standards, so they are not safe to use.
You should stop using the projectors immediately and contact Santajoy for further instructions.
Check for model numbers EZ-Illuminations Galaxy or EZ-Illuminations Northern Lights on the product.
We’ve drafted a message you can send Santajoy to request your refund or repair — edit it as you like.
Subject: Recall Z-1884-2018 — Santajoy Santajoy Hello, I own a Santajoy that is covered by recall Z-1884-2018 from Santajoy. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
