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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 50 of 500 Results *
Firm: Philips Medical Systems
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Allura Xper FD20 Biplane; Model Number: 722008; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20; Model Number: 722006; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10/10; Model Number: 722005; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10; Model Number: 722003; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10F; Model Number: 722002; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Product Name: Allura Xper FD10C; Model number: 722001; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10/10; Model Number: 722027; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/20; Model Number: 722038; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/10; Model Number: 722029; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20; Model Number: 722028; 2 01/13/2026 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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