Class II — Potential Health Hazard

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...

Date: May 17, 2021
Company: Cytocell Ltd.
Status: Terminated
Source: FDA (Device)

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

Affected (7 states)Not affected

About Cytocell Ltd.

Cytocell Ltd. has 14 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report