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Epi proColon

Epigenomics AG · Model Control Kit · UDI-DI 04260400670029

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0
510(k) clearances
31
Adverse events (1 deaths)
2
Recalls
11
Facilities

Description

Epi proColon Control Kit

Recalls

DateFirmReason
2017-11-02Epigenomics AgThe diagnostic test kit may produce invalid test runs which may delay test results.
2017-04-28Exact Sciences CorporationExact Sciences is correcting all Sample Mixer v2 Upgrade units because of incidents of Sample Mixer door damage, which has occurred when the Sample Holder opens during a run and th

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.