The Recall Desk
SevereFDA (Devices)·Z-1157-2025·Announced 2025-02-26

Philips Azurion 7 B12 examination tables recalled due to patient fall risk

Philips Medical Systems is recalling Azurion 7 B12 examination tables due to a mattress-related patient fall risk. The recall affects 602 total units, including 94 in the US and 508 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: This is an FDA Class I medical device recall, which establishes a minimum severity score of 4. However, no deaths, serious injuries, or hospitalizations have been reported in the source text. The hazard is characterized as a theoretical possibility rather than a documented incident, placing it at Severe rather than Critical.

Plain-English summary

Philips Medical Systems Nederland B.V. is recalling Azurion 7 B12 patient examination tables. The affected devices include three catalog numbers: 722067, 722225, and 722235 (the latter for overseas use only). Approximately 602 units have been distributed worldwide, including 94 units in the United States.

The recall was issued as a Class I device recall due to a possibility that patients could fall from the examination table. This fall hazard is related to the mattress used on the patient table. No injuries or illnesses have been reported in connection with this recall.

Healthcare facilities that use these examination tables should verify whether they have any of the affected devices by checking the serial numbers provided in the recall notice. The full list of affected serial numbers and additional details are available through the FDA's recalls database.

The recalled product

Product
Azurion 7 B12; Catalog numbers: (1) 722067, (2) 722225, (3) 722235 (OUS ONLY).
Manufacturer
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Category
Medical Device — Patient Examination 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) 722067
  • (2) 722225
  • (3) 722235 (OUS ONLY)
  • UDI-DI: (1) 00884838085350
  • (2) 00884838099265
  • (3) 00884838116788
  • Serial Numbers: (1) 26
  • 150
  • 190
  • 278
  • 69
  • 141
  • 115
  • 221
  • 148
  • 46
  • 36
  • 42
  • 98
  • 123

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 →

Same hazard · fall hazard

See all →