Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

RET Distal Probe. Used in Fluorescence in situ hybridization (FISH) Recalled by Cytocell Ltd. Due to DNAs used during the manufacture of two affected...

Date: May 24, 2023
Company: Cytocell Ltd.
Status: Ongoing
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

RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome.

Quantity: 61 units

Why Was This Recalled?

DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 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