FDA recall, , Moderate risk
Fresh Roast Systems ColorTrack
The Fresh Roast Systems ColorTrack could allow human access to infrared laser light levels in excess of its safety classification.
Summary by Recall Canary from the FDA notice
What happened
Fresh Roast Systems Inc of Key Biscayne, Florida, began a recall of the Fresh Roast Systems ColorTrack instrument, model number BENCH R-100, on April 15, 2026. The FDA added the recall to its Enforcement Report on June 11, 2026. A defect in the product's manufacture could, under very rare specific misuse circumstances, potentially allow human access to infrared laser light levels in excess of the safety Classification of the product.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the list below, then check the codes the FDA notice also names.
Fresh Roast Systems ColorTrack. Model Name: ColorTrack.
- Model
- BENCH
From the FDA notice
Model Number: BENCH R-100
Recall details
- Company began the recall
- Sold in
U.S.
- Company
- Fresh Roast Systems IncKey Biscayne, Florida
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99111
- Recall number
- Z-2280-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
