PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. 2024-06-05 Health serious FDA
Health · FDA · Recall #FDA-Z-1896-2024
Philips Allura Xper FD10 system with an ADN7NT patient table. Model Number: 722010,… Recall
Issued June 5, 2024 · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
In June 2024, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalled the Philips Allura Xper FD10 system with an ADN7NT patient table. Model Number: 722010,…, 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
When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.
What you should do
- 1 Stop using Philips Allura Xper FD10 system with an ADN7NT patient table. Model Number: 722010,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. 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 MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Health
- Recall date
- June 5, 2024
- Units affected
- Not reported
- Sold at
- Domestic: OK International: India, Spain, U.A.E.
- Recall number
- FDA-Z-1896-2024
- Made in
- Netherlands
- Issuing agency
- FDA
In context
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has 17 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.