Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region Probe Recalled by Cytocell Ltd. Due to The device may show unexpected locus specific signals...
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 Cytocell Ltd. directly.
Affected Products
CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region Probe, Model Number LPU004-A. analyte specific reagent for in vitro diagnostics
Quantity: 50
Why Was This Recalled?
The device may show unexpected locus specific signals in addition to those at 22q. Users may observe faint additional locus specific signals at 20p12/13.
Where Was This Sold?
This product was distributed to 7 states: CA, IL, MO, NY, PA, TX, UT
About Cytocell Ltd.
Cytocell Ltd. has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report