Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Centricity Laboratory Core Lab System 4.1 The Centricity Laboratory System Recalled by GE Healthcare It Due to The Centricity Laboratory removes free-text notes on a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Healthcare It directly.
Affected Products
Centricity Laboratory Core Lab System 4.1 The Centricity Laboratory System is intended to be an information system designed to support the clinical and administrative activities associated with the provision and utilization of clinical laboratory services and facilities, e.g., the storing and delivering of analytical results. It is a specially designed data program application (software), which is supplied for installation in existing mainframe or decentralized computers or a computer network.
Quantity: 17
Why Was This Recalled?
The Centricity Laboratory removes free-text notes on a master panel when the user deletes the slave panel. The deletion of a slave panel will (auto slash) the corresponding test (item) results on the master panel. Additionally, the displayed and HL7 results show neither the appropriate abnormal flag value nor the reference range values, when using large_num.g >7 to report numeric results.
Where Was This Sold?
This product was distributed to 6 states: GA, MN, NY, OH, TN, TX
About GE Healthcare It
GE Healthcare It has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report