Amerx Health Care Corp.: Medical Device Recall in 2014 - (Recall #: Z-0498-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Amerigel Post-op Surgical Kits Wound management

Product Classification:

Class II

Date Initiated: September 26, 2014

Date Posted: December 10, 2014

Recall Number: Z-0498-2015

Event ID: 69394

Reason for Recall:

Formulation deviation

Status: Terminated

Product Quantity: 79,677

Code Information:

Model # A2002, Lot #s: JCA0086, JCA0087, JCA0088, JCA0089, JCA0090, JCA0091, JCA0092, JCA0093, JCA0094, JCA0095, JCA0096, JCA0097, JCA0098, JCA0099, JCA0100, JCA0101, JCA0102, JCA0103, JCA0104, JCA0105, JCA0106

Distribution Pattern:

Worldwide Distribution - US (nationwide) including states of: AK, AL, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, ME, MD, MI, MT, MO, NC, NH, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WY, WV, Virgin Islands, Puerto Rico, Guam, Hawaii and District of Columbia and Internationally to: Canada, England, Africa, and Australia.

Voluntary or Mandated:

Voluntary: Firm initiated