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U.S. Department of Health and Human Services

Medical Device Recalls

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91 to 100 of 500 Results *
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Product Description
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FDA Recall
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ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/10; System Code: 722029; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/20 OR Table; System Code: 722039; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/15; System Code: 722058; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/15 OR Table; System Code: 722059; 2 03/27/2026 FEI # 3042175844
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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