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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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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 DIMMs (Dual In-line ... 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.
Philips Allura (Model Numbers 722010, 722012, 722026, 722027, 722028, 722029, 722035) and Philips Az... 2 04/06/2022 Philips North America Llc
Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without a... 2 03/04/2022 Philips North America Llc
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 FD series with Software Version Number: 2.1.x- intended for Vascular, cardiovasc... 2 12/22/2021 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
The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular a... 2 09/14/2021 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
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