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.
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 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
- patient-fall-risk
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.
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