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.
The agency’s classification
FDA (Devices): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. 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.
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