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FDA Medical Device Recalls (openFDA)

Foundation Medicine, Inc.: FoundationOne Companion Diagnostic (F1CDx)

Recall number
Z-1890-2025
Recalling firm
Foundation Medicine, Inc.
Product
FoundationOne Companion Diagnostic (F1CDx)
Status
Open, Classified
Initiated
2024-06-18
Posted
2025-05-30
Terminated
not on file
Reason
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.
Root cause
Software design
Action
On June 18, 2024, amended reports were sent to customers. It was to alert customers to an amended report that was recently released on 6/18/24. The new report replaces the report of 2/11/24. Additional contact was made on June 20, 2024 to communicate the error and provide the updated report to the customer.
Quantity
2 units
Distribution
US Nationwide distribution in the state of MI.
Lot, serial or model codes
Report Numbers: ORD-XXXXX77-01, ORD-XXXXX91-01. Note: The above characters have been redacted to minimize patient information disclosure.
510(k) numbers
not on file
PMA numbers
["P170019"]
Product code
PQP
Firm FEI
3010679023
Firm city
Cambridge
Firm state
MA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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