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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 34 Results
510(K) Number: K102005
 
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The following systems are only affected if a Laird chiller is installed (11NC: 98960021599): Allura ... 2 04/14/2017 Philips Electronics North America Corporation
Allura Xper FD OR Table, Ceiling version only; 722035; imaging applications. 2 02/05/2016 Philips Electronics North America Corporation
Allura Xper FD10; Model Number: 722003; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10/10; Model Number: 722005; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20; Model Number: 722006; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20 Biplane; Model Number: 722008; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10; Model Number: 722010; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10/10; Model Number: 722011; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20; Model Number: 722012; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20 Biplane; Model Number: 722013; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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