FDA recall record

Geneoscopy ColoSense Test Kit, Part No. 80-001, component of ColoSense test recall — FDA Z-2077-2025

Multiple plate failures documented as a result of the Low Positive Template Control being too high and out of range using the affected lot of ColoSense…

Class IIclassification
Z-2077-2025official record ID
Jul 9, 2025report date

Recall record at a glance

Official recordZ-2077-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmGeneoscopy, Inc.
Report dateJul 9, 2025
Recall initiation dateMay 20, 2025
Quantity10 units
LocationSaint Louis, MO, United States

Official product description

ColoSense Test Kit, Part No. 80-001, component of ColoSense test

Why the product was recalled

Multiple plate failures documented as a result of the Low Positive Template Control being too high and out of range using the affected lot of ColoSense Test Kit.

Distribution information

US Nationwide distribution in the state of Missouri.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.