FDA recall Z-1625-2020

Gentell, Inc · Class II · device

Product

Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing.

Reason for recall

During an FDA audit, it was discovered that the product was not properly registered with FDA.

Distribution

Worldwide distribution  US Nationwide distribution in the states of AL, CA, FL, IA, IL, KY, MA, MI, MN, NC, NJ, NY, OH, OK, PA, Puerto Rico, RI, SC, TN, TX, WI and countries of Panama, South Africa, Bahrain, Spain, Mexico, Costa Rica, Romania.

Key facts

Status
Ongoing
Initiation date
2020-02-27
Report date
2020-04-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Bristol, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1625-2020