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Recall Observatory FDA recall evidence

Device product

Gentell Hydrogel Ag 2x2, model no GEN-11220 - 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.

Z-1623-2020

February 27, 2020

Class II

Product summary

Firm
Gentell, Inc
Event
Event 85034
Status
Ongoing
Classification
Class II
Quantity
53,134
Official record key
device-enforcement:Z-1623-2020

Official wording

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

Code information: 1134117 1101918 1107518 1114918 1121118 1127718 1131018 1133218 1135118 1105919 1118819 1121419 1124919

Distribution pattern: 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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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