Reported Dec 28, 2016 · Terminated
Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes
Ultroid Technologies, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Ultroid Technologies, Inc. · 3140 W Kennedy Blvd Suite 103 · Tampa, FL · 33609-3175
Is this the product you have?
- Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes
- Lot codes and dates
- ALL serial numbers and lot numbers sold since 2003.
- Amount recalled
- 1,129
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was 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)
This product could cause temporary or reversible health problems — stop using it.
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