Class II — Potential Health Hazard

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

greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA Recalled by Greiner Bio-One North America, Inc. Due to Some of the tubes may be incorrectly labeled.

Date: March 31, 2023
Company: Greiner Bio-One North America, Inc.
Status: Completed
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 Greiner Bio-One North America, Inc. directly.

Affected Products

greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA, 13x100 pink cap-black ring, non-ridged, 24 racks of 50 pcs., 1200 pcs in total, Item #456003

Quantity: 36,000 pieces (30 full cases)

Why Was This Recalled?

Some of the tubes may be incorrectly labeled.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Greiner Bio-One North America, Inc.

Greiner Bio-One North America, Inc. has 16 total recalls tracked by RecallDetector.

Related Recalls

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