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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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Allura Xper IGTS Fixed Systems
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2
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09/30/2024
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FEI # 3006648320 Philips North America
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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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FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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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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FEI # 3016618143 Philips North America Llc
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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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FEI # 3016618143 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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FEI # 3016618143 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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FEI # 3002807880 Philips Medical Systems Nederlands
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Cardio Vascular-Allura Centron, system code 722400
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2
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03/13/2020
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FEI # 1218950 Philips North America, LLC
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Allura CV20, system code 722031
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2
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03/13/2020
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FEI # 1218950 Philips North America, LLC
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Allura Exper FD Series. System codes
722003
722010
722022
722005
722011
722019
722001
722002...
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2
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03/13/2020
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FEI # 1218950 Philips North America, LLC
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AIIura Xper F010 DR Table, System Code 722022
Vascular, cardiovascular and neurovascular imaging...
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2
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09/21/2018
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FEI # 1218950 Philips Electronics North America Corporation
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