DeviceSignal · Recall classified
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA classified a device recall on 2026-08-05 · Class II · Z-2893-2026
EventRecall classified
Effective2026-08-05
ClassificationClass II
On 2026-08-05 the FDA classified a device recall from PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. as Class II. Product: Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional…. Recall Z-2893-2026. The firm initiated it on 2026-06-17. This reports the classification FDA published on that date.
Reported facts
- Recall number
- Z-2893-2026
- Classification
- Class II
- Classified on
- 2026-08-05
- Initiated on
- 2026-06-17
- Firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Reason
- Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
- Product
- Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. 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-2893-2026- 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
7e649c0641a148322a9b91730145145f13c0a92557c43394d8ced493424727f4- 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)