Reported Aug 19, 2026 · Ongoing · Updated Sep 4, 2026
Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional…
Philips Medical Systems Nederland B.v.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 6 · Best · N/A
Is this the product you have?
- Allura Xper FD
- Model Numbers722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system
- Lot codes and dates
- Model Numbers
722026722027722028722029722035722038722039722058
- Software VersionR8.2
- UDI Numbers
944 of 944 codes
(01)00884838054202(21)1756(01)00884838054202(21)1569(01)00884838059115(21)100(01)00884838059115(21)239(01)00884838054202(21)520(01)00884838054202(21)1956(01)00884838054189(21)683(01)00884838054196(21)351(01)00884838054202(21)129(01)00884838059115(21)305(01)00884838054196(21)332(01)00884838054202(21)1233(01)00884838054202(21)2206(01)00884838054202(21)1690(01)00884838054202(21)928(01)00884838054189(21)155(01)00884838054202(21)317(01)00884838054202(21)1774(01)00884838054202(21)2502(01)00884838054202(21)869(01)00884838054202(21)668(01)00884838054189(21)618(01)00884838054189(21)1051(01)00884838054189(21)1052(01)00884838054202(21)406(01)00884838054202(21)540(01)00884838054202(21)548(01)00884838054202(21)1017(01)00884838054202(21)590(01)00884838054189(21)654(01)00884838054189(21)786(01)00884838054196(21)216(01)00884838054196(21)230(01)00884838054202(21)596(01)00884838054202(21)1957(01)00884838054202(21)110(01)00884838054202(21)2261(01)00884838054189(21)1132(01)00884838054226(21)115(01)00884838059115(21)259(01)00884838054202(21)173(01)00884838054202(21)866(01)00884838054202(21)1310(01)00884838059115(21)203(01)00884838054202(21)1043(01)00884838054189(21)458(01)00884838054202(21)466(01)00884838054226(21)42(01)00884838054202(21)1077(01)00884838059115(21)373(01)00884838054202(21)877(01)00884838054202(21)896(01)00884838054202(21)987(01)00884838054202(21)995(01)00884838054202(21)1343(01)00884838054202(21)1439(01)00884838059115(21)111(01)00884838054202(21)895(01)00884838054202(21)265(01)00884838054202(21)305
- Model Numbers
- Amount recalled
- 4,252 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Firmware issue potentially leading to loss of geometry movements.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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