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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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Z-2291-2026 - Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
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2
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06/01/2026
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FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Z-2290-2026 - Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
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2
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06/01/2026
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FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Z-2289-2026 - Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
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2
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06/01/2026
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FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Z-2288-2026 - Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
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2
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06/01/2026
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FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Z-2287-2026 - Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
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2
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06/01/2026
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FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Z-2286-2026 - Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
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2
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06/01/2026
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FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Z-2285-2026 - Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
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2
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06/01/2026
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FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Z-2284-2026 - Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
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2
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06/01/2026
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FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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