[Recalled] Burstberry Laser Projection Series — The User Remote Interlock Dongle provided with the E-Stop Remote is not suffici… | FDA 2019-07-10
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Burstberry Laser Projection Series |
|---|---|
| Brand / manufacturer | Gk Photonics Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2097-2019 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 10 July 2019 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.