RecallHawk
Class II Recall

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

Fresh Roast Systems Inc

Summary

The FDA issued a Class II for Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-1 by Fresh Roast Systems Inc. Reason: 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 .

Details

Source

Device Recall

External ID

Z-2280-2026

Action Date

2026-06-17

Status

Ongoing

Category

device

Product Description

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

Lot/Code Info: Only Model Number provide. Model Number: BENCH R-100

Quantity Affected: 38

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.

Distribution

U.S.

Type: FDA Mandated

Recall Initiated: 2026-04-15

Company

Fresh Roast Systems Inc

Key Biscayne, FL

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 228 device recalls issued in the same week, part of 403 device-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Fresh Roast Systems Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Fresh Roast Systems Inc have FDA actions?

This is the only FDA action we have on record for Fresh Roast Systems Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-2280-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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