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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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UNIQ FD; Model Numbers: 722028
The Philips UNIQ is intended for use on human patients to perform:...
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2
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01/30/2016
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Philips Electronics North America Corporation
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UNIQ FD OR table; Model Number 722035
The Philips UNIQ is intended for use on human patients to p...
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2
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01/30/2016
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Philips Electronics North America Corporation
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UNIQ 1.0: UNIQ FD10, 722026; UNIQ FD10/10, 722027; UNIQ FD20, 722028; UNIQ FD20/10 biplane, 722029; ...
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2
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08/26/2016
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Philips Electronics North America Corporation
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The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular a...
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2
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09/14/2021
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Philips North America Llc
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The Allura Xper series is intended for use on human patients to perform:
"Vascular, cardiovascular ...
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2
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09/14/2021
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Philips North America Llc
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System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Xper FD20/15 722039 Allura Xper FD20/...
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2
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09/18/2024
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Philips X-Ray Systems, Allura Xper with R8.2.16
Product Usage: The Allura Xper FD1O and Allura X...
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2
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03/07/2016
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Philips Electronics North America Corporation
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Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System produc...
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2
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03/04/2022
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Philips North America Llc
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Philips Allura Xper System: Interventional Fluoroscopic X-Ray System
Product No.: 722026, 722027, 7...
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2
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06/21/2021
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Philips Medical Systems Nederlands
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Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC c...
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2
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02/16/2024
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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