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
G1D1842032G1D1842035G1C17X2022G1D1852039Not Available*G1D1922084G1B16X2002G1D1972106G1D18X2058G1D18Y2066G1B1912074G1B1772014G1C1782016G1D1842033G1D18Z2071G1D1962102G1D1962104G1D1862041G1D18Y2068G1D1972107G1D18Z2069Not Available*G1D19X2118G1D1982112Not Available*G1D1862043G1D18Y2065Not Available*G1D1962101G1C17X2026G1D1832029G1D1962105G1B1772012G1D1832030G1B1772012G1D1852038Not AvailableG1D1842031G1C17X2023G1C1782017G1D1892054G1D1932088G1C17X2024G1D1882049G1D1882048G1D1912077G1D1932089GID194092G1923001923G1793810017G1D1882052G1D1922080G1D1862045G1D1882051G1C1792020G1D1892055G1D1932090G1B1742006G1D18Z2070G1D1862042
- Serial Numbers
- 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.
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