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.
- Hazard
- fall-hazard
- mattress-defect
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.
Related recalls
Same category
- SevereMedline Spinal Block Kits Recalled for Data Integrity and Efficacy Issues
FDA (Devices) · 2026-06-03
- SevereAbiomed Automated Impella Controller recalled for motor control and pump failure risks
FDA (Devices) · 2026-06-03
- HighGE APEXPRO and CARESCAPE Telemetry Systems Risk Loss of Patient Monitoring
FDA (Devices) · 2026-06-03
- CriticalMedline spinal anesthetic kits recalled for quality and efficacy concerns
FDA (Devices) · 2026-06-03
- SevereMedline spinal anesthesia kits recalled for bupivacaine quality issues
FDA (Devices) · 2026-06-03