The Recall Desk

Manufacturer

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

202 recalls in our database name PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. as the manufacturing or recalling firm.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

51–75 of 202

  • Severity pendingFDA (Devices)·Z-1091-2026·2026-01-21

    Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label des

    Pending LLM rewrite. Source: FDA_DEVICE Z-1091-2026.

    Product
    Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Numbers: 722063, 722221. 2. Azurion 3 M15. Model Numbers: 722064, 722222, 722280. 3. Azurion 5 M12. Model Num
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1075-2026·2026-01-21

    Allura Xper FD20; Model Number: 722028;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1075-2026.

    Product
    Allura Xper FD20; Model Number: 722028;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1069-2026·2026-01-21

    Allura Xper FD10/10; Model Number: 722011;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1069-2026.

    Product
    Allura Xper FD10/10; Model Number: 722011;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1066-2026·2026-01-21

    Allura Xper FD20; Model Number: 722006;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1066-2026.

    Product
    Allura Xper FD20; Model Number: 722006;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1065-2026·2026-01-21

    Allura Xper FD10/10; Model Number: 722005;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1065-2026.

    Product
    Allura Xper FD10/10; Model Number: 722005;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1070-2026·2026-01-21

    Allura Xper FD20; Model Number: 722012;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1070-2026.

    Product
    Allura Xper FD20; Model Number: 722012;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1062-2026·2026-01-21

    Product Name: Allura Xper FD10C; Model number: 722001;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1062-2026.

    Product
    Product Name: Allura Xper FD10C; Model number: 722001;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1074-2026·2026-01-21

    Allura Xper FD10/10; Model Number: 722027;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1074-2026.

    Product
    Allura Xper FD10/10; Model Number: 722027;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1064-2026·2026-01-21

    Allura Xper FD10; Model Number: 722003;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1064-2026.

    Product
    Allura Xper FD10; Model Number: 722003;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1068-2026·2026-01-21

    Allura Xper FD10; Model Number: 722010;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1068-2026.

    Product
    Allura Xper FD10; Model Number: 722010;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1067-2026·2026-01-21

    Allura Xper FD20 Biplane; Model Number: 722008;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1067-2026.

    Product
    Allura Xper FD20 Biplane; Model Number: 722008;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1077-2026·2026-01-21

    Allura Xper FD20/20; Model Number: 722038;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1077-2026.

    Product
    Allura Xper FD20/20; Model Number: 722038;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1073-2026·2026-01-21

    Allura Xper FD10; Model Number: 722026;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1073-2026.

    Product
    Allura Xper FD10; Model Number: 722026;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1076-2026·2026-01-21

    Allura Xper FD20/10; Model Number: 722029;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1076-2026.

    Product
    Allura Xper FD20/10; Model Number: 722029;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1063-2026·2026-01-21

    Allura Xper FD10F; Model Number: 722002;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1063-2026.

    Product
    Allura Xper FD10F; Model Number: 722002;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1079-2026·2026-01-21

    Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models:

    Pending LLM rewrite. Source: FDA_DEVICE Z-1079-2026.

    Product
    Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. Azurion 3 M15. Model Number: 722230. 3. Azurion 5 M12. Model Number: 722231. 4. Azurion 5 M20. Model Number: 722232. 5.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1072-2026·2026-01-21

    Allura Xper FD20 OR Table; Model Number: 722023;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1072-2026.

    Product
    Allura Xper FD20 OR Table; Model Number: 722023;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • Severity pendingFDA (Devices)·Z-1071-2026·2026-01-21

    Allura Xper FD20 Biplane; Model Number: 722013;

    Pending LLM rewrite. Source: FDA_DEVICE Z-1071-2026.

    Product
    Allura Xper FD20 Biplane; Model Number: 722013;
    Category
    Medical Device
    Distribution
    Distributed nationwide