Reported Jul 29, 2015 · Terminated
GE Healthcare, Precision MPi fluoroscopic imaging systems.
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 MPi fluoroscopic imaging systems.
- Lot codes and dates
- Mfg Lot or Serial #
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
- Mfg Lot or Serial #
- 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.
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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