Philips North America Llc: Intera 1.0T Power/Pulsar, Magnetic Resonance System.

Hazard

Patient support table floor plate may be incorrectly installed.

Details from the source

Reason for recall: Patient support table floor plate may be incorrectly installed. Distribution: Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Andorra, Argentina, Armenia, Australia, Austria, Bahamas, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia-Herzegovina, Botswana, Brazil, Bulgaria, Cambodia, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, C¿te D'Ivoire, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Rep, Ecuador, Egypt, Esto Quantity: 19 units Lot/code info: Model No. 781103; UDI-DI n/a; Serial No. 7062, 7164, 7102, 7113, 7084, 10381, 7097, 10383, 10384, 10391, 7150, 7074, 7237, 7190, 7198, 10413, 10382, 7103, 10071.

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.