Philips Allura Centron patient table mattress defect poses fall risk
Philips is recalling Allura Centron patient examination tables due to a mattress defect that poses a fall risk. Eighty units have been distributed internationally.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The FDA classified this recall as Class I, which per the scoring rubric requires a minimum severity score of 4 (Severe). The hazard involves patient fall risk from a medical equipment defect.
Plain-English summary
Philips Medical Systems Nederland B.V. is recalling Allura Centron patient examination tables (catalog number 722400) due to a mattress defect. The mattress used on the patient table may cause patients to fall from the table during examination or use.
Eighty units have been distributed internationally. The FDA classified this as a Class I recall, indicating a serious public health concern.
Facilities and medical institutions using the affected tables should contact the manufacturer immediately for repair or replacement instructions. The recall number is Z-1161-2025.
The recalled product
- Product
- Cardio Vascular-Allura Centron; Catalog number: 722400 (OUS ONLY).
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Affected units
- 80
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Catalog numbers: (1) 722400
- UDI-DI: No UDI
- Serial Numbers: 531
- 314
- 432
- 376
- 496
- 315
- 491
- 361
- 389
- 486
- 427
- 547
- 330
- 444
- 441
- 536
- 479
- 555
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 20 recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 20 products in this recall →Related recalls
Same manufacturer · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
See all →- HighPhilips Azurion Rystem X-Ray System Software Recall for Image Quality Issues
FDA (Devices) · 2026-08-19
- HighPhilips Azurion Fluoroscopy System Recall for Software Image Quality Issues
FDA (Devices) · 2026-08-19
- HighPhilips Allura Xper FD Fluoroscopic X-Ray System Recalled for Firmware Issue
FDA (Devices) · 2026-08-19
- SeverePhilips Allura X-Ray Systems Recalled Over Unauthorized Hard Disk Drives
FDA (Devices) · 2026-08-12
- HighPhilips Azurion interventional fluoroscopic X-ray systems recalled for potential hardware failures
FDA (Devices) · 2026-08-12
Same hazard · fall injury risk
See all →- SevereCyberknife Treatment Delivery System Collimator Docking Failure Risk
FDA (Devices) · 2026-07-08
- SeverePhilips recalls Allura patient table mattress due to fall hazard
FDA (Devices) · 2025-02-26
- HighKnee walker recalled for tiller separation that may cause falls
FDA (Devices) · 2024-07-24
- High2024 East to West RV Recall: Detachable Rear Ladder Poses Injury Risk
NHTSA · 2023-09-22
- HighTreadmill Safety Tether Circuit Defect May Prevent Emergency Stop
FDA (Devices) · 2022-12-14