Philips Azurion 3 M12 Medical Table Recalled for Patient Fall Risk
Philips is recalling Azurion 3 M12 patient tables due to possibility of patient falling from the table related to the mattress. The recall affects 263 units distributed in the US and 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: This is an FDA Class I recall, which per guidance requires a minimum severity score of 4. However, no injuries, illnesses, or reported incidents are documented in the source text, and the hazard remains theoretical, placing this in the Severe rather than Critical range.
Plain-English summary
Philips Medical Systems Nederland B.V. is recalling Azurion 3 M12 patient tables, catalog numbers 722063 and 722221. The recall addresses a possibility of patient falling from the table related to the mattress used on the patient table.
The affected distribution includes 263 total units: 26 in the United States and 237 internationally across more than 100 countries and territories. Affected equipment is identified by catalog numbers 722063 and 722221, and specific serial numbers.
This is classified as an FDA Class I recall.
The recalled product
- Product
- Azurion 3 M12; Catalog numbers: (1) 722063, (2) 722221.
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Medical Device — Patient Table
- Hazard
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) 722063
- (2) 722221
- UDI-DI: (1) 00884838085275
- (2) 00884838099203
- Serial Numbers: (1) 96
- 122
- 132
- 131
- 108
- 84
- 98
- 56
- 64
- 101
- 29
- 139
- 61
- 75
- 40
- 77
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 Allura Xper FD Fluoroscopic X-Ray System Recalled for Firmware Issue
FDA (Devices) · 2026-08-19
- HighPhilips Azurion Fluoroscopy System Recall for Software Image Quality Issues
FDA (Devices) · 2026-08-19
- HighPhilips Fluoroscopy System Recall Over Hard Disk Drive Issue
FDA (Devices) · 2026-08-12
- SeverePhilips Allura X-Ray Systems Recalled Over Unauthorized Hard Disk Drives
FDA (Devices) · 2026-08-12
Same hazard · patient fall risk
See all →- HighPhilips Brilliance iCT SP CT Systems Patient Support Table Descent
FDA (Devices) · 2025-10-01
- SeverePhilips Azurion 5 M20 tables recalled due to patient fall risk
FDA (Devices) · 2025-02-26
- SeverePhilips Azurion 3 M15 Patient Tables Recalled for Patient Fall Risk
FDA (Devices) · 2025-02-26
- SevereAzurion 7 M20 Patient Tables Recalled for Patient Fall Risk
FDA (Devices) · 2025-02-26
- HighPhilips Intera 1.5T MRI Patient Support Table Floor Plate Installation Defect
FDA (Devices) · 2024-04-24
Similar recalls
- HighAzurion 3 M12 systems recalled over tables that may move unexpectedly
FDA (Devices) · 2026-02-18
- HighAzurion 3 M15 systems recalled over tables that may move unexpectedly
FDA (Devices) · 2026-02-18
- HighAzurion 5 M12 systems recalled over tables that may move unexpectedly
FDA (Devices) · 2026-02-18
- HighPhilips Azurion patient tables recalled for finger entrapment risk
FDA (Devices) · 2025-02-12
- HighAzurion 7 M12 systems recalled over tables that may move unexpectedly
FDA (Devices) · 2026-02-18
- HighPhilips Azurion patient tables recalled for finger entrapment hazard
FDA (Devices) · 2025-02-12