Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-2227-2026 - Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, ... | 2 | 05/21/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-2229-2026 - Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044... | 2 | 05/21/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Z-2228-2026 - Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10/10 (722005, 722011, 722027),... | 2 | 05/21/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
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