FDAAugust 22, 2024device

System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 M20 722236 Azurion 7 B20 722235 Azurion 7 B12 722234 Azurion 7 M20 722233 Azurion 7 M12 722228 Azurion 5 M20 722227 Azurion 5 M12 722226 Azurion 7 B20 722225 Azurion 7 B12 722224 Azurion 7 M20 722223 Azurion 7 M12 722222 Azurion 3 M15 722221...

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

The hazard

Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or bolts) which May Result in Parts Falling and/or Part of the Cable Hose Dropping, and result in injury.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

008848381105710088483811056400884838116801008848381167880088483811677100884838116764008848380992340088483809922700884838099272008848380992650088483809925800884838099241

Recall history

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

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