United StatesMerge PACS and Merge OrthoPACS medical imaging diagnostic workstations, software version V9.5 (UDI (01)00842000101239(10)9.5.0(11)260409), distributed nationwide in the U.S. in California, Florida, Kentucky, Nebraska and Washington (20 units), are affected. They were recalled because a software issue may cause measurements to be displayed inaccurately.
What's being recalled
Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation
Recalling firm: Merge Healthcare, Inc., Hartland, WI, United States.
How to identify it
Software version V9.5 - UDI (01)00842000101239(10)9.5.0(11)260409
The hazard
Software issue may cause measurements to be displayed inaccurately.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the states of California, Florida, Kentucky, Nebraska, Washington.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)