Fresh Recalls

FDAClass II · Medical device · Recall Z-2280-2026 · Recalled June 17, 2026

Fresh Roast Systems ColorTrack recall — Fresh Roast Systems Inc

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Fresh Roast Systems ColorTrack
Company / brand
Fresh Roast Systems
Lot / serial / date codes
Only Model Number provide. Model Number: BENCH R-100
Distribution
U.S.
Agency product description and boundaries

Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Fresh Roast Systems ColorTrack recall status

3. Open the official notice or contact

Official recall ID
Z-2280-2026
Brand
All Fresh Roast Systems recalls
Classification
Class II
Units affected
38
Recall status
Ongoing
Initiated
FDA Mandated

Affected products

Companies & origin

Recalling firm location
Key Biscayne, FL, United States
Firm address
200 Ocean Lane Dr Apt 806, N/A, 33149-1447

Identifying details (verbatim from the notice)

Product codes / lots
Only Model Number provide. Model Number: BENCH R-100
Distribution
U.S.
Firm notified the public via
N/A
FDA event ID
99111
Recall initiated
April 15, 2026
FDA classified
June 11, 2026
FDA report date
June 17, 2026

Other medical device recalls from around the same time

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 15, 2026 at 6:00 PM UTC.

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