Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

PrepIT Q2A Kit Recalled by DNA Genotek Inc. Due to Reagents were shipped to customers after the Use...

Date: June 24, 2020
Company: DNA Genotek Inc.
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 DNA Genotek Inc. directly.

Affected Products

PrepIT Q2A Kit, Model PT-Q2A-96 containing component reagent AG (PT-QAG-96) 1.4mL and ST (PT-QST-96) 2.9mL - Product Usage: used for the removal of SDS and other inhibitors from samples collected using DNA Genotek oral sample collection kits.

Quantity: 74

Why Was This Recalled?

Reagents were shipped to customers after the Use by data indicated on its labeling.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About DNA Genotek Inc.

DNA Genotek Inc. has 3 total recalls tracked by RecallDetector.

Related Recalls

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