Class II — Potential Health Hazard

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

ActCel advanced bleeding control Topical Hemostatic Dressing 2in X 2in Recalled by Coreva Health Science LLC Due to Coreva Health Science, LLC. is recalling ActCel Hemostatic...

Date: May 18, 2015
Company: Coreva Health Science LLC
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 Coreva Health Science LLC directly.

Affected Products

ActCel advanced bleeding control Topical Hemostatic Dressing 2in X 2in (5cm X 5cm) 4in X 4in Sterile Contents Soluble Regenerated Cellulose For Bleeding Control For external topical and temporary use only Sterility of contents guaranteed unless individual envelope is damaged or opened. Store at room temperature (41F-104F). Do not autoclave.

Quantity: 180,900

Why Was This Recalled?

Coreva Health Science, LLC. is recalling ActCel Hemostatic Dressing due to customer literature and web sites promoting that it can help control bleeding from open wounds and in body cavities. ActCel is indicated as a prescription device for management of topical wounds and to temporarily control external surface bleeding.

Where Was This Sold?

This product was distributed to 6 states: AZ, FL, NY, TX, VA, WA

Affected (6 states)Not affected

About Coreva Health Science LLC

Coreva Health Science LLC has 1 total recall tracked by RecallDetector.

Related Recalls

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