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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 40 Results
510(K) Number: K141979
 
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UNIQ FD; Model Numbers: 722028 The Philips UNIQ is intended for use on human patients to perform:... 2 01/30/2016 Philips Electronics North America Corporation
UNIQ FD OR table; Model Number 722035 The Philips UNIQ is intended for use on human patients to p... 2 01/30/2016 Philips Electronics North America Corporation
UNIQ 1.0: UNIQ FD10, 722026; UNIQ FD10/10, 722027; UNIQ FD20, 722028; UNIQ FD20/10 biplane, 722029; ... 2 08/26/2016 Philips Electronics North America Corporation
The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular a... 2 09/14/2021 Philips North America Llc
The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular ... 2 09/14/2021 Philips North America Llc
Philips X-Ray Systems, Allura Xper with R8.2.16 Product Usage: The Allura Xper FD1O and Allura X... 2 03/07/2016 Philips Electronics North America Corporation
Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System produc... 2 03/04/2022 Philips North America Llc
Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: 722026, 722027, 7... 2 06/21/2021 Philips Medical Systems Nederlands
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC c... 2 02/16/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC c... 2 02/16/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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