Class II — Potential Health Hazard

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

V8 Immunodisplacement Kit REF 1803 Recalled by Helena Laboratories, Corp. Due to Due to microbial growth causing interference with interpretation.

Date: April 6, 2022
Company: Helena Laboratories, Corp.
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 Helena Laboratories, Corp. directly.

Affected Products

V8 Immunodisplacement Kit REF 1803

Quantity: 51 kits

Why Was This Recalled?

Due to microbial growth causing interference with interpretation.

Where Was This Sold?

This product was distributed to 4 states: FL, MO, OH, TX

Affected (4 states)Not affected

About Helena Laboratories, Corp.

Helena Laboratories, Corp. has 11 total recalls tracked by RecallDetector.

Related Recalls

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