Reported Feb 17, 2021 · Terminated

GE Healthcare Precision 600FP, Classical R&F (radiographic and fluoroscopic) System - Product Usage: Intended for use…

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?

  • GE Healthcare Precision 600FP, Classical R&F (radiographic and
  • fluoroscopic) System - Product UsageIntended for use by a qualified/trained doctor or technologist on both adult and pediatric subjects taking diagnostic radiographic and fluoroscopic exposures of the whole body, skull, spinal column, chest, abdomen, extremities and other body parts
Lot codes and dates
  • Serial Numbers

    113 of 113 codes

    • G1D1842032
    • G1D1842035
    • G1C17X2022
    • G1D1852039
    • Not Available*
    • G1D1922084
    • G1B16X2002
    • G1D1972106
    • G1D18X2058
    • G1D18Y2066
    • G1B1912074
    • G1B1772014
    • G1C1782016
    • G1D1842033
    • G1D18Z2071
    • G1D1962102
    • G1D1962104
    • G1D1862041
    • G1D18Y2068
    • G1D1972107
    • G1D18Z2069
    • Not Available*
    • G1D19X2118
    • G1D1982112
    • Not Available*
    • G1D1862043
    • G1D18Y2065
    • Not Available*
    • G1D1962101
    • G1C17X2026
    • G1D1832029
    • G1D1962105
    • G1B1772012
    • G1D1832030
    • G1B1772012
    • G1D1852038
    • Not Available
    • G1D1842031
    • G1C17X2023
    • G1C1782017
    • G1D1892054
    • G1D1932088
    • G1C17X2024
    • G1D1882049
    • G1D1882048
    • G1D1912077
    • G1D1932089
    • GID194092
    • G1923001923
    • G1793810017
    • G1D1882052
    • G1D1922080
    • G1D1862045
    • G1D1882051
    • G1C1792020
    • G1D1892055
    • G1D1932090
    • G1B1742006
    • G1D18Z2070
    • G1D1862042
Amount recalled
113 units

Where it was sold

Why it was recalled

GE Healthcare has become aware of a potential safety issue associated with the improper installation of the Precision 600FP monitor suspension. A partial detachment of the monitor suspension could result in potential injury to a patient or operator.

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.

Free recall alerts

Get alerted about new GE Healthcare, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 18, 2022 · Data as of Sep 19, 7:39 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.