Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by Luminex Corporation Due to An incorrect control board and firmware installed in...
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 Luminex Corporation directly.
Affected Products
Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in clinical laboratories. Scanner Label/Labeling: JADAK JDK-2330 REV B 170512-017
Quantity: 153 (140 U.S. and 13 O.U.S.)
Why Was This Recalled?
An incorrect control board and firmware installed in some of the Hand Held Barcode Scanners could result in sample/patient mismatch or duplicate results (from other patients specimens) for a patient order.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Luminex Corporation
Luminex Corporation has 39 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report