FDAJanuary 13, 2025device

Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Possibility of the patient falling from the table related to the mattress used on the patient table.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

008848380852680088483809925800884838116771

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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