Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine, Inc. Due to Two (2) reports were sent to customers with...

Date: June 18, 2024
Company: Foundation Medicine, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Foundation Medicine, Inc. directly.

Affected Products

FoundationOne Companion Diagnostic (F1CDx)

Quantity: 2 units

Why Was This 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.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Foundation Medicine, Inc.

Foundation Medicine, Inc. has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report