Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including Recalled by Ultroid Technologies, Inc. Due to Products are not designed, qualified, manufactured, and/or managed...
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 Ultroid Technologies, Inc. directly.
Affected Products
Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes
Quantity: 1,129
Why Was This Recalled?
Products are not designed, qualified, manufactured, and/or managed under a state of control per internal quality system procedures and external laws, regulations, directives, standards, and/or guidance (such as 21 CFR 820 Quality System Regulation)
Where Was This Sold?
This product was distributed to 33 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, KS, LA, ME, MD, MI, MN, NE, NV, NH, NJ, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA
About Ultroid Technologies, Inc.
Ultroid Technologies, Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report