DeviceSignal · Recall classified
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA classified a device recall on 2026-08-10 · Class II · Z-2928-2026
EventRecall classified
Effective2026-08-10
ClassificationClass II
On 2026-08-10 the FDA classified a device recall from PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. as Class II. Product: Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039…. Recall Z-2928-2026. The firm initiated it on 2026-06-29. This reports the classification FDA published on that date.
Reported facts
- Recall number
- Z-2928-2026
- Classification
- Class II
- Classified on
- 2026-08-10
- Initiated on
- 2026-06-29
- Firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Reason
- Firmware issue potentially leading to loss of geometry movements.
- Product
- Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.
Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_enforcement
- Source record
Z-2928-2026- Snapshot hash
ab5ada73bf212eb52a548aab0968a0fcee42807c61b0350e60e24bb6e2beed72- Source URL
- https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
- Observed
- 2026-09-08T16:22:09.483Z
- Transform
fda_device_enforcement_to_recall v1- Event rule
fda_device_recall_classified v1- Event key
9e0637759c1234727c47e49f68c5dc57c0b7852ac4d63ef69630c1964d277f17- Signal type
device_recall.classified
Source terms that apply
- This is not a public alerting service and must not be used to notify patients or the public
- We do not report whether a recall is still open; FDA does not maintain that after classification
- Nothing here is a medical or clinical decision aid
- Not affiliated with, endorsed by, or certified by the FDA
Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)