Reported Jul 29, 2015 · Terminated
GE Healthcare Precision RXi 23A/32A Analog 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 23A/32A Analog System
- Lot codes and dates
- Mfg Lot or Serial #
00000001386MC200000002109MC700000001010MC800000001337MC500000002212MC900000001720MC200000001098MC300000001454MC800000001082MC700000001266MC600000001656MC800000003661MC6
- 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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