Class II — Potential Health Hazard

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

VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring Recalled by Greiner Bio-One North America, Inc. Due to Blood collection tubes may experience a clotting issue.

Date: August 13, 2021
Company: Greiner Bio-One North America, 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 Greiner Bio-One North America, Inc. directly.

Affected Products

VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged

Quantity: 962,400 tubes

Why Was This Recalled?

Blood collection tubes may experience a clotting issue.

Where Was This Sold?

This product was distributed to 15 states: AL, AZ, CO, CT, FL, IL, MD, MA, MI, MO, NM, NC, PA, TX, VA

Affected (15 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