CLASS II Device recall · Reported 13 Jun 2018 · FDA Enforcement Report
Santajoy Ornament & Giftware Co. products recalled
Santa JOY Ornament & Giftware is recalling Santajoy Ornament & Giftware Co., Ltd E-Z Illuminations Northern Lights E-Z Illuminations, distributed nationwide in the US. The recall was initiated on 21 Nov 2017 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1884-2018
- FDA event ID
- 78975
- Recalling firm
- Santa JOY Ornament & Giftware, Dongguan City, N/A
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 21 Nov 2017
- FDA classified
- 1 Jun 2018
- Reported
- 13 Jun 2018
- Type
- FDA Mandated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 21 Nov 2017 | Recall initiated by company | |
| 1 Jun 2018 | Classified by FDA | +192 days |
| 13 Jun 2018 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
It was discovered that the product units it imported may, at peak levels, emit radiation that exceeds the federal standard for Class IIIa products.
Product as listed by the FDA
Santajoy Ornament & Giftware Co., Ltd E-Z Illuminations Northern Lights E-Z Illuminations Galaxy Laser projectors that emit various colors and light patterns for entertainment and decorative purposes.
Where it was distributed
USA (nationwide) distribution
Questions about this recall
Why was it recalled?
It was discovered that the product units it imported may, at peak levels, emit radiation that exceeds the federal standard for Class IIIa products.
Which lots are affected?
Model No: EZ-Illuminations Galaxy , EZ-Illuminations Northern Lights
Where was it sold?
USA (nationwide) distribution
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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