What should someone who has this product do?

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100) and recall number Z-2280-2026, then follow Fresh Roast Systems Inc's recall instructions.

Has Fresh Roast Systems Inc had other FDA recalls or enforcement actions?

This is the only FDA action Argus HQ has on file for Fresh Roast Systems Inc so far. Argus ingests new FDA enforcement records daily.

Recall Record: Class II Recall: Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model… by Fresh Roast Systems Inc

Here's the summary: Fresh Roast Systems Inc recalled Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100 on 2026-06-17. FDA classified this action as a Class II recall (recall number Z-2280-2026). Reason for recall: 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.. Recall status: Ongoing. This is a device-category FDA recall record.

Key facts

Recalling firm	Fresh Roast Systems Inc
Manufacturer	Not disclosed in the FDA record.
Brand name	Not disclosed in the FDA record.
Product description	Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100
Classification	Class II
Recall number	Z-2280-2026
Report date	Not disclosed in the FDA record.
Status	Ongoing
Reason for recall	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.

What consumers should do

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100 -- and the recall number Z-2280-2026. If it matches, stop using or distributing it and contact Fresh Roast Systems Inc or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do.

What this classification means

FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is Fresh Roast Systems Inc and the affected product is described in FDA's record as: Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100. FDA's stated reason for the recall is: 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.. The recall is tracked under FDA recall number Z-2280-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do. Recall status can change while FDA and the recalling firm continue corrective actions, so checking the firm's own notice for the most current guidance is recommended.

Fresh Roast Systems Inc’s FDA history

Argus HQ has recorded 1 total FDA action tied to Fresh Roast Systems Inc: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

What was recalled and why?: Fresh Roast Systems Inc recalled Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100. FDA's record states the reason for recall as: 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.. The recall is logged under FDA recall number Z-2280-2026 with a Class II classification.
How serious is this recall?: FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote.
What should someone who has this product do?: Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100) and recall number Z-2280-2026, then follow Fresh Roast Systems Inc's recall instructions.
Has Fresh Roast Systems Inc had other FDA recalls or enforcement actions?: This is the only FDA action Argus HQ has on file for Fresh Roast Systems Inc so far. Argus ingests new FDA enforcement records daily.

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Full FDA history for Fresh Roast Systems Inc

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). Recall Record: Class II Recall: Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model… by Fresh Roast Systems Inc. Digital Empire LLC. Retrieved from https://argushq.ai/recall/fda-recall-fresh-roast-systems-inc-z-2280-2026

MLA

"Recall Record: Class II Recall: Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model… by Fresh Roast Systems Inc." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/recall/fda-recall-fresh-roast-systems-inc-z-2280-2026.

Chicago

Argus HQ Research. "Recall Record: Class II Recall: Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model… by Fresh Roast Systems Inc." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/recall/fda-recall-fresh-roast-systems-inc-z-2280-2026.

BibTeX

@misc{argushq_argushq_ai_recall_fda_recall_fresh_roast_systems_inc_z_2280_2026_2026,
  title = {Recall Record: Class II Recall: Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model… by Fresh Roast Systems Inc},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/recall/fda-recall-fresh-roast-systems-inc-z-2280-2026},
  note = {Accessed: July 13, 2026}
}

Source: FDA.gov — Recalls ↗