Philips Medical Systems North America Co. Phillips AD 7 Patient table supplied with Allura Xper FD10 and Allura Xper FD10/10. Product is non-tilting but can be purchased with a tilt option. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AD 7 Patient table supplied with Allura Xper FD10 and Allura Xper FD10/10. Product is non-tilting but can be purchased with a tilt option.
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
Part number 9896 002 04432
Products Sold
Part number 9896 002 04432
Philips Medical Systems North America Co. Phillips is recalling AD 7 Patient table supplied with Allura Xper FD10 and Allura Xper FD10/10. Product is non-tilting b due to Potential for radiologic patient table to become immobile and unable to move again due to force sensor sensitivity to electromagnetic radiation.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for radiologic patient table to become immobile and unable to move again due to force sensor sensitivity to electromagnetic radiation.
Recommended Action
Per FDA guidance
On 03/22/2004, firm sent letters via certified mail to notify customers of issue. Letter advises customers of potential risk for patients and users, and states to not use system for critical examinations or treatments if table movements suddenly stops or makes a freeing movement. The letter indicates a representative will contact customer for installation of a Hardware filter, free of charge, to prevent Electromagnetic interference (EMI) from affecting the force sensor. Please contact Philips at 1-800-722-9377 #5, #4, #1.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026