Agendia MammaPrint, Catalog Numbers MP01, MP US version 03
FDA Recall Z-1321-2010 · Posted 2010-04-12
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Recalling FirmAgendia Inc
Recall StatusTerminated
Product CodeNYI
Date Initiated2010-03-03
Date Terminated2010-06-18
Product Quantity107
Reason for Recall
Over a period of about 6 months in about 15% of results provided Agendia has been "over reporting" the chance of metastasis risk being 29% risk of recurrence instead of 10% risk.
This over reporting of risk did not cause direct injury to patients. However, if used by physicians as the sole basis for decision-making, affected patients may have received unnecessary therapy.
Firm Action
Communication with physicians was initiated by the firm's Chief Medical Officer on March 3, 2010. The firm's representatives will meet with treating physicians in person while having the corrected results in hand to inform each in person of the action, to allow a decision of the best course of action. Physicians will be provided with background information on the issue at hand and corrected results.
As follow up, the physician would receive a corrected report per patient by FedEx in order to register the reception of corrected information.
Because each user received a personal visit, no other contact information was planned or provided by Agendia.
Root Cause
Other
Distribution Pattern
Nationwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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