Burstberry Laser Projection Series recall
Burstberry Laser Projection Series
Why was Burstberry Laser Projection Series recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Burstberry
- Product
- Burstberry Laser Projection Series
- Recalling firm
- Gk Photonics Inc
- Quantity
- N/A
- Distribution
- Unknown
- Recall date
- August 14, 2019
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)