United StatesMerge PACS and Merge OrthoPACS medical imaging diagnostic workstations (affected versions 9.4, 9.4 P01, and 9.4 P02; UDIs include (01)00842000101215(10)9.4.0.P01(11)250916 and (01)00842000101154(10)9.4.0.P02(11)260302) are included in the recall. They were recalled because thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
What's being recalled
Merge PACS, medical imaging diagnostic workstation
Merge OrthoPACS, medical imaging diagnostic workstation
Recalling firm: Merge Healthcare, Inc., Hartland, WI, United States.
How to identify it
UDI (01)00842000101215(10)9.4.0.P01(11)250916, (01)00842000101154(10)9.4.0.P02(11)260302 with Affected Versions: 9.4, 9.4 P01, and 9.4 P02. UDI/DI (01)00842000101154(10)9.4.0.P02(11)260302, with Affected Versions: 9.4, 9.4 P01, and 9.4 P02.
The hazard
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
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
Worldwide distribution - US Nationwide and the countries of Canada, and UK.
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)