Philips North America Llc 2024-04-24 Health serious FDA
Health · FDA · Recall #FDA-Z-1553-2024
Achieva 3.0T, Magnetic Resonance System. Recall
Issued April 24, 2024 · Philips North America Llc
In April 2024, Philips North America Llc recalled the Achieva 3.0T, Magnetic Resonance System., a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Patient support table floor plate may be incorrectly installed.
What you should do
- 1 Stop using Achieva 3.0T, Magnetic Resonance System. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Philips North America 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
- Philips North America Llc
- Category
- Health
- Recall date
- April 24, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Andorra, Argentina, Armenia, Australia, Austria, Bahamas, Bahr
- Recall number
- FDA-Z-1553-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Philips North America Llc has 34 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.