Philips Allura Xper X-Ray Systems Recall: Incorrect Bolt in Fluoroscopy Kits
Philips recalls Allura Xper systems (R8.1 with Poly-G Stand) due to incorrect bolt in LTE kits. Model numbers 722010, 722012, 722013; serial numbers 111 138 467 817 2928 269. Affected units may have safety risks during use.
Lower-risk recall
A half-threaded bolt was included in the LTE kits instead of the correct full-threaded bolt.
Contact the company
What happened, in plain English
Philips is recalling Allura Xper X-Ray systems with specific model numbers and serial ranges because a half-threaded bolt was included instead of the correct full-threaded bolt in some kits. This could lead to improper assembly and potential safety issues during medical procedures. Read more at govinfonow.com/recall/54256-philips-allura-xper-x-ray-systems-recall-incorrect-bolt-in.
Source Summary by GovInfoNow · govinfonow.com/recall/54256-philips-allura-xper-x-ray-systems-recall-incorrect-bolt-in · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2716-2024
Cite this page
“Philips Allura Xper X-Ray Systems Recall: Incorrect Bolt in Fluoroscopy Kits.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54256-philips-allura-xper-x-ray-systems-recall-incorrect-bolt-in. Based on FDA recall #Z-2716-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2716-2024%22&limit=1).
Why it’s dangerous
The incorrect half-threaded bolt can cause improper assembly of the system. This may lead to instability or malfunction during medical procedures, but the hazard is not described as causing immediate injury or death in normal use.
Who’s affected
Medical facilities using Philips Allura Xper systems with model numbers 722010, 722012, or 722013 and the listed serial numbers are most at risk. These systems are used in interventional fluoroscopy procedures.
How to tell if you have this one
Check for model numbers 722010, 722012, or 722013 on the system. Also verify the serial numbers listed: 111 138 467 817 2928 269.
- Brand
Philips- Category
Medical device
What to do — step by step
Check Model Numbers
Identify if your system has model numbers 722010, 722012, or 722013.
Verify Serial Numbers
Confirm the serial number matches the range 111 138 467 817 2928 269.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 2 states.
FDA distribution: “Worldwide - US Nationwide distribution in the states of IL and OR. The countries of Hungary, Ireland, Poland, UK.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Illinois, Oregon.
Recall timeline
FDA published this recall 20 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2716-2024 (August 8, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2716-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.