Medical Device Recalls
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1 result found
Recall Number: Z-2953-2024 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional Fluoroscopic X-Ray ... | 2 | 09/04/2024 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
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