Class II — Potential Health Hazard

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

Genesys Diluent Reagent Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech USA) Due to lack of 510K

Date: November 1, 2018
Company: Clark Laboratories, Inc. (dba,Trinity Biotech USA)
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 Clark Laboratories, Inc. (dba,Trinity Biotech USA) directly.

Affected Products

Genesys Diluent Reagent, REF 01-03-0019 intended to be used with automated high performance liquid chromatography (HPLC) systems employing ion exchange chromatography. For in vitro diagnostic use only.

Quantity: 463 units

Why Was This Recalled?

lack of 510K

Where Was This Sold?

This product was distributed to 6 states: AZ, IL, MD, NJ, UT, WV

Affected (6 states)Not affected

About Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Clark Laboratories, Inc. (dba,Trinity Biotech USA) has 9 total recalls tracked by RecallDetector.

Related Recalls

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