Philips Medical Systems Nederland B.v. Allura Xper FD20/15 OR Table recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
The hazard: Device safety concern
A device recall was filed for this product. For anything implanted or relied on daily, the clinician comes before the paperwork.
What the notice says: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.
Recall details
- Recall number
- Z-1672-2026
- Published
- April 8, 2026
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Philips Medical Systems Nederland B.v.
- Product type
- Medical devices
- Units affected
- 2 units (2 US, 6 OUS)
- Distribution
- Nationwide
- Made in
- Netherlands
- Lot / code info
- System Code: 722059; UDI: 00884838059122; System Serial Number: 33, 7, 35, 40, 38, 41, 37, 2;
- UPC codes
- 00884838059122
Products covered by this recall
Allura Xper FD20/15 OR Table; System Code: 722059;
Check your product
The notice names 7 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
UPC / barcode
Read the twelve digits under the barcode on the package.
- 00884838059122
Serial number
On the rating plate, often next to the date of manufacture.
- 33
- 35
- 40
- 38
- 41
- 37
Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Device
Philips Medical Systems Nederland B.v. — A device recall was filed for this product. For anything implanted or relied on daily, the clinician comes before the paperwork.
- Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
- If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.
- Ask the supplier or clinic that provided it what the remedy is in your case.
- If you are a facility, quarantine affected stock and log the correction.
Claiming on a recalled device
Device recalls are tracked by serial and lot number, so your claim moves faster if you lead with those.
- Have the model, catalogue, lot and serial numbers ready before you call — they are on the device label or its box.
- Ask explicitly whether your unit is in the affected range; many recalls cover only part of a model line.
- If you need the device daily, ask what interim arrangement they offer while the remedy is carried out.
- Log the date, the name and the reference number of every call. Device recalls can run for months.
Company contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Veenpluis 6, Best
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was Philips Medical Systems Nederland B.v. medical devices recalled?
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: UPC 00884838059122. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
Can I get my money back?
Have the model, catalogue, lot and serial numbers ready before you call — they are on the device label or its box.
Where was the recalled product sold?
It was distributed nationwide.
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