GE Healthcare, LLC 2022-04-20 Health serious FDA
Health · FDA · Recall #FDA-Z-0919-2022
MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) 3101010-401, c)… Recall
Issued April 20, 2022 · GE Healthcare, LLC
In April 2022, GE Healthcare, LLC recalled the MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) 3101010-401, c)…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Two scenarios may cause edits to measurements and diagnosis statements can be lost after a test is Signed in the MUSE NX web client.
What you should do
- 1 Stop using MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) 3101010-401, c)… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact GE Healthcare, LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- GE Healthcare, LLC
- Category
- Health
- Recall date
- April 20, 2022
- Units affected
- Not reported
- Sold at
- US and Australia, Austria, Bahrain, Belgium, Brazil, Canada, Denmark, England, France, Germany, Ireland, Italy, Korea, Malaysia, Netherlands
- Recall number
- FDA-Z-0919-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- GE Healthcare, LLC has 14 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.