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FDA (Device enforcement)Recalled 2024-03-12class ii

Philips North America Llc: Intera 0.5T Standard, 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: 14 units Lot/code info: Model No. 781101; UDI-DI n/a; Serial No. 6047, 6018, 6023, 6027, 6031, 6044, 6060, 10306, 6015, 6061, 6025, 6054, 6001, 6066.

Source

Official record: FDA (Device enforcement)

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

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