Fresh Roast Systems recalls ColorTrack BENCH R-100 models due to rare misuse potentially exposing users to unsafe infrared laser levels. No immediate action needed but check for model number.
A defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which 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.
Fresh Roast Systems is recalling its ColorTrack BENCH R-100 model because a defect could allow infrared laser exposure under very rare misuse conditions. This risk is extremely uncommon and does not require immediate action.
The ColorTrack device has a defect that could, under very rare misuse circumstances, allow infrared laser light levels exceeding safety classifications. This means the laser could potentially cause injury if the device is used in a way that the user is exposed to the laser beam without proper safeguards.
Users of the ColorTrack BENCH R-100 model who might accidentally expose themselves to infrared laser light during rare misuse scenarios. Most users are not at risk as the hazard requires specific, uncommon actions.
Check for the model number BENCH R-100 on the device. The product was sold as a ColorTrack instrument by Fresh Roast Systems Inc.
Look for the model number BENCH R-100 on the device to confirm it is recalled.
The hazard is extremely rare and requires specific misuse circumstances. Most users are not at risk.
No immediate action is required. The recall does not mandate stopping use.
Check for the model number BENCH R-100 on the device.
We’ve drafted a message you can send Fresh Roast Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2280-2026 — Fresh Roast Systems Fresh Roast Systems Hello, I own a Fresh Roast Systems that is covered by recall Z-2280-2026 from Fresh Roast Systems. 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.
