Reported Jul 29, 2015 · Terminated

GE Healthcare Precision RXi Digital system

GE Healthcare

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 · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • GE Healthcare Precision RXi Digital system
Lot codes and dates
  • Mfg Lot or Serial #
    • 00000003510MC5
    • 00000004082MC4
    • 00000001524MC8
    • 00000004565MC8
    • 00000004022MC0
    • 00000001590MC9
    • 00000002033MC9
    • 00000004021MC2
    • 00000001528MC9
    • 00000001975MC2
    • 00000002235MC0
    • 00000003739MC0
    • 00000001147MC8
    • 00000001280MC7
    • 00000000953MC0
    • 00000001645MC1
    • 00000001319MC3
    • 00000002255MC8
    • 00000004585MC6
    • 00000001473MC8
    • 00000001292MC2
    • 00000004110MC3
    • 00000001354MC0
    • 00000001744MC2
    • 00000002104MC8
    • 00000001020MC7
    • 00000001093MC4
    • 00000001429MC0
    • 00000001453MC0
    • 00000001407MC6
    • 00000001388MC8
    • 00000001374MC8
    • 00000001296MC3
    • 00000001652MC7
    • 00000001381MC3
    • 00000004024MC6
    • 00000004160MC8
    • 00000001380MC5
    • 00000001969MC5
    • 00000001100MC7
    • 00000001170MC0
    • 00000004108MC7
    • 00000003844MC8
    • 00000001288MC0
    • 00000004702MC7
    • 00000004703MC5
    • 00000001394MC6
    • 00000001527MC1
    • 00000001428MC2
    • 00000004597MC1
    • 00000004027MC9
    • 00000003966MC9
Amount recalled
788 (701 US; 87 OUS)

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

  • Nationwide
  • DC

Why it was recalled

A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.

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 Aug 3, 2017 · Data as of Sep 19, 4:48 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.