FDA recall record

Foundation Medicine FoundationOne Companion Diagnostic (F1CDx) recall — FDA Z-1890-2025

Two (2) reports were sent to customers with an incorrect negative claim on the claims page; the device variant information was displayed correctly in the…

Class IIclassification
Z-1890-2025official record ID
Jun 11, 2025report date

Recall record at a glance

Official recordZ-1890-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmFoundation Medicine, Inc.
Report dateJun 11, 2025
Recall initiation dateJun 18, 2024
Quantity2 units
LocationCambridge, MA, United States

Official product description

FoundationOne Companion Diagnostic (F1CDx)

Why the product was recalled

Two (2) reports were sent to customers with an incorrect negative claim on the claims page; the device variant information was displayed correctly in the tumor profiling section of both FDA-approved test reports.

Distribution information

US Nationwide distribution in the state of MI.

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.

Related recall records

Other records from the same recalling company are shown first when available.