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

Philips North America Llc: Intera 1.5T Explorer/Nova Dual, 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: 12 units Lot/code info: Model No. 781108; UDI-DI n/a; Serial No. 8918, 10035, 8803, 10037, 9025, 10022, 10638, 10640, 8743, 8651, 10091, 8690.

Source

Official record: FDA (Device enforcement)

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

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