Philips ALLURA Xper FD20 OR Table Recall
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Philips is voluntarily recalling 196 units of the ALLURA Xper FD20 OR Table due to potential issues with X-ray imaging not initiating properly via the wired foot switch.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 15, 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, cpsc, 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 FD20 OR Table. This recall is classified as Class II and was initiated voluntarily by the firm.
Which Products Are Affected
The affected products are the ALLURA Xper FD20 OR Table with the following System Codes: (1) 722015, (2) 722023, and (3) 722035. A total of 196 units are involved, with 73 units in the US and the rest distributed outside the US. Specific details include:
- For System Code 722015: UDI: N/A; Serial Numbers: 12, 16, 2, 8, 23, 3, 13
- For System Code 722023: UDI: 00884838059085; Serial Numbers: 49, 41, 142, 110, 12, 179, 124, 27, 98, 66, 118, 117, 138, 42, 64, 116, 127, 175, 75, 82, 83, 46, 35, 109, 146, 33, 165, 169, 101, 103, 129, 10, 105, 90, 107, 100, 47, 159, 137, 119, 164, 70, 95, 177, 158, 5, 86, 34, 132, 9, 108, 121, 31, 112, 173, 114, 170, 172, 4, 14, 85, 13, 88, 25, 87, 94, 57, 125, 73, 106, 67, 16, 96, 58, 38, 141, 32, 84, 68, 134, 79, 52, 56, 69, 37, 21, 53, 123, 157, 102, 126, 145, 144, 15, 135, 152, 149, 60, 150
- For System Code 722035: UDI: 00884838054240; Serial Numbers: 119, 126, 169, 72, 124, 161, 183, 242, 245, 246, 46, 196, 52, 236, 147, 172, 123, 74, 59, 60, 88, 30, 216, 212, 85, 21, 47, 222, 121, 131, 145, 127, 38, 187, 243, 143, 244, 125, 117, 100, 57, 247, 34, 165, 252, 101, 89, 192, 111, 128, 227, 144, 174, 28, 84, 130, 263, 132, 25, 98, 134, 35, 226, 190, 3, 6, 1, 249, 109, 251, 207, 158, 160, 237, 163, 79, 248, 253, 94, 80, 250, 154, 69, 97, 148, 170, 195, 26, 122, 96, 107, 142, 58, 166, 235, 230, 83, 53, 32, 164, 56, 40, 10, 11, 62, 265, 221, 257, 255, 229, 256, 254, 261, 260, 238, 113, 258, 241, 188, 259, 267, 167, 204, 43, 33, 37, 104, 233, 114, 108, 153, 70, 65, 191, 77, 110, 225, 75, 76, 193, 185, 186, 129, 103, 71, 151, 92, 201, 208, 149, 205, 19, 50, 51, 61, 211, 99, 12, 15, 198, 82, 105, 136, 194, 23, 200, 116, 48, 13, 106, 95, 206, 168, 203, 146, 81, 156, 45, 173, 49, 64, 171, 184, 102, 17, 215, 29, 231, 16, 202
The products were distributed nationwide in the US and to various international countries.
What You Should Do
Users should follow the initial firm notification, which was sent via letter, for instructions on this voluntary recall initiated by Philips Medical Systems Nederland B.V.
Why This Matters
This recall ensures the reliable operation of medical devices used in procedures, potentially preventing issues that could affect patient care. It highlights the importance of addressing malfunctions in healthcare equipment to maintain safety standards.
Source
Attribution to FDA: Recall number Z-1665-2026, available on the FDA website under event ID 98434.
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 (2,777 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to April 15, 2026.
Frequently Asked Questions
Common questions about this FDA recall.