Reported Apr 13, 2022 · Ongoing

Signa 1.5T TwinSpeed Magnetic Resonance Imaging System

GE Healthcare, LLC

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: GE Healthcare, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • Signa 1.5T TwinSpeed Magnetic Resonance Imaging System
Lot codes and dates
  • System IDs
    • MMIMR01
    • 213748HDMR
    • 714125MR
    • 561218MR1
    • 918523MR1
    • 304766MR1
    • 082427030026
    • 082427080007
    • 082427020017
    • 376569401MR
Amount recalled
10 units

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide

Why it was recalled

There is potential for the images to be flipped left to right.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:36 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.