Sequencing Agent SEQ0067, component of FoundationOne CDx (F1CDx)
FDA Recall Z-1927-2026 · Posted 2026-04-22
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Recalling FirmFoundation Medicine, Inc.
Recall StatusOpen, Classified
Product CodePQP
Date Initiated2026-03-20
Product Quantity163 units
Reason for Recall
Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants
Firm Action
Foundation Medicine notified consignees via emailed letter on about 03/20/2026. Consignees were instructed to review, complete, sign and return the provided business reply form and review inventory and identify affected units, quarantine those units, and return to the FMI Boston Warehouse quarantine location via standard laboratory transfer practices. Consignees were also instructed to forward the notification to anyone within the facility that should be informed and if there is any impact that requires this notice to be forwarded to another facility, including facilities where units of inventory may have been transferred, contact that facility and provide them with this letter. Consignees were asked to retain the letter with laboratory records made aware that Foundation Medicine will work with the supplier of these components to replace impacted units.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the states of Massachusetts and North Carolina.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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