FDA recall Z-0577-2026

Foundation Medicine, Inc. · Class II · device

Product

FoundationOne CDx (F1CDx), RAL-0003 version 31.0

Reason for recall

Reports were sent to customers without the companion diagnostic (CDx) Claims Page. Claims pages were distributed via amended reports within 7 days of the issue occurrence.

Distribution

US Nationwide distribution to states of: AL, AZ, CA, FL, GA, IL, IN, KS, KY, ME, MN, MO, MS, MT, NC, NJ, NV, NY, OK, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV. OUS International to countries: Japan, Singapore.

Key facts

Status
Ongoing
Initiation date
2022-11-08
Report date
2025-12-03
Voluntary/Mandated
Voluntary: Firm initiated
Location
Cambridge, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0577-2026