Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
QUANTA-Lyser 240 EIA Recalled by Inova Diagnostics Incorporated Due to The device power supply was not manufactured according...
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 Inova Diagnostics Incorporated directly.
Affected Products
QUANTA-Lyser 240 EIA, Part #GS0241. The instrument is a fully automated, high-throughput, bench top system designed for clinical use to automate slide and reagent barcode reading, sample dilution and distribution, reagent pipetting and dispensing, slide and plate washing, dispensing slide mounting medium in the preparation for microscope analysis, and photometric measurement of microwell plates.
Quantity: 1 instrument
Why Was This Recalled?
The device power supply was not manufactured according to specification which can result in the loss of the protective grounding of the instrument.
Where Was This Sold?
There was no U.S. distribution. Distribution was made to Panama and United Kingdom.
About Inova Diagnostics Incorporated
Inova Diagnostics Incorporated has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report