Class II — Potential Health Hazard

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

Amerigel Hydrogel Gauze Dressing 2 x 2 Recalled by Amerx Health Care Corp. Due to Nonapproved labeling claims (Sterile)

Date: February 25, 2015
Company: Amerx Health Care Corp.
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 Amerx Health Care Corp. directly.

Affected Products

Amerigel Hydrogel Gauze Dressing 2 x 2, A5002. Wound Management.

Quantity: 6,491 units

Why Was This Recalled?

Nonapproved labeling claims (Sterile)

Where Was This Sold?

This product was distributed to 44 states: AL, AK, AZ, AR, CA, CO, CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MS, MO, MT, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WY

Affected (44 states)Not affected

About Amerx Health Care Corp.

Amerx Health Care Corp. has 10 total recalls tracked by RecallDetector.

Related Recalls

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