Reported Jul 29, 2015 · Terminated

GE Healthcare Precision 500D Classical R & F 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 500D Classical R & F system.
Lot codes and dates
  • Mfg Lot or Serial #

    681 of 681 codes

    • 00000002243MC4
    • 00000017545MC9
    • 00000001018MC1
    • 00000001083MC5
    • 00000003942MC0
    • 00000001707MC9
    • 00000001110MC6
    • 0000000B2055KJ
    • 00000001283MC1
    • 00000002163MC4
    • 00000002189MC9
    • 00000002190MC7
    • 00000000895MC3
    • 00000001165MC0
    • 00000001107MC2
    • 00000004224MC2
    • 00000001902MC6
    • 00000004278MC8
    • 00000000930MC8
    • 00000000945MC6
    • 00000004162MC4
    • 00000004211MC9
    • 00000001560MC2
    • 00000001293MC0
    • 00000003575MC8
    • 00000003619MC4
    • 00000001204MC7
    • 00000001205MC4
    • 00000003702MC8
    • 00000003885MC1
    • 00000001207MC0
    • 00000004018MC8
    • 00000001128MC8
    • 00000004382MC8
    • 00000004578MC1
    • 00000001385MC4
    • 00000003406MC6
    • 00000000868MC0
    • 00000000949MC8
    • 00000001369MC8
    • 00000003932MC1
    • 00000001006MC6
    • 00000001361MC5
    • 00000001441MC5
    • 00000000888MC8
    • 00000001097MC5
    • 00000003622MC8
    • 00000001058MC7
    • 00000004422MC2
    • 00000001511MC5
    • 00000001614MC7
    • 00000001245MC0
    • 00000003700MC2
    • 00000003701MC0
    • 00000001360MC7
    • 00000001155MC1
    • 00000001588MC3
    • 00000003617MC8
    • 00000002387MC9
    • 00000003928MC9
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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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

Notice updated Aug 3, 2017 · Data as of Sep 19, 4:47 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.