Reported Dec 28, 2016 · Terminated

Ultroid Procedure Pack including the Ultroid Sterile Disposable 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 Procedure Pack including the Ultroid Sterile Disposable Probes.
Lot codes and dates
  • ALL serial numbers and lot numbers sold since January 14, 2003.
Amount recalled
52,084

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 11, 2019 · Data as of Sep 19, 5:21 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.