Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Gentell Hydrogel Ag 2x2 Recalled by Gentell, Inc Due to During an FDA audit, it was discovered that...
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 Gentell, Inc directly.
Affected Products
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.
Quantity: 53,134
Why Was This Recalled?
During an FDA audit, it was discovered that the product was not properly registered with FDA.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Gentell, Inc
Gentell, Inc has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report