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Recall Observatory FDA recall evidence

Device product

FoundationOne Companion Diagnostic (F1CDx)

Z-1747-2025

April 09, 2025

Class II

Product summary

Firm
Foundation Medicine, Inc.
Event
Event 96621
Status
Ongoing
Classification
Class II
Quantity
4 units
Official record key
device-enforcement:Z-1747-2025

Official wording

Reason: Four (4) total reports were sent to customers with clinically relevant variants requiring amendment, one (1) of which with an incorrect negative CDx claim. The remaining three (3) with tumor profiling result changes did not impact CDx indications.

Code information: ORD-XXXXX28-01 ORD-XXXXX98-01 ORD-XXXXX29-01 ORD-XXXXX99-01 Note: The above characters have been redacted to minimize patient information disclosure.

Distribution pattern: Worldwide - US Nationwide distribution in the states of GA, NY and the country of Russia.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Four (4) total reports were sent to customers with clinically relevant variants requiring amendment, one (1) of which with an incorrect negative CDx claim. The remaining three (3) with tumor profiling result changes did not impact CDx indications.