Recall of Philips ALLURA Xper FD10 OR Table for Imaging Issues
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Philips is voluntarily recalling two units of the ALLURA Xper FD10 OR Table due to potential failures in X-ray imaging when using the wired foot switch.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 16, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch on the ALLURA Xper FD10 OR Table. This is a voluntary recall initiated by the firm.
Which Products Are Affected
The affected products are the ALLURA Xper FD10 OR Table with System Codes: (1) 722022 and (2) 722033. There are 2 units affected, with 1 in the US and 1 outside the US. Specific codes include: For System Code 722022, UDI: 00884838059078 and System Serial Number: 6; For System Code 722033, UDI: 00884838054233 and System Serial Number: 1. The recall number is Z-1667-2026, and distribution includes nationwide in the US and various international locations.
What You Should Do
Consumers should contact the recalling firm, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., as initial notification was made via letter.
Why This Matters
This recall involves medical devices that could affect X-ray imaging reliability in healthcare settings, potentially leading to procedural issues. It is classified as a Class II recall, indicating possible temporary or reversible health consequences.
Source
Attribution: FDA. For more information, refer to the FDA recall details.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,233 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to April 16, 2026.
Frequently Asked Questions
Common questions about this FDA recall.