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 Recalled by Greiner Bio-One North America, Inc. Due to Some of the blood collection tubes show clotting...

Date: December 9, 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

greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF 456087P

Quantity: 889,200 pcs.

Why Was This Recalled?

Some of the blood collection tubes show clotting due to variation of Lithium Heparin.

Where Was This Sold?

This product was distributed to 10 states: FL, IL, MO, NM, NY, NC, PA, TN, TX, VA

Affected (10 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