The Recall Desk

Hazard

Imaging Failure recalls

46 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
46
Critical
0
Severe
1
Most recent
2026-06-10

Of the 46 imaging failure recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (2%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all imaging failure recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–25 of 46

  • HighFDA (Devices)·Z-2289-2026·2026-06-10

    Philips Azurion 7B20/15 systems may show unusable dark fluoroscopy images

    Philips Azurion 7B20/15 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable. 156 units affected.

    Product
    Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2286-2026·2026-06-10

    Philips Azurion 5M12 systems may show unusable dark fluoroscopy images

    Philips Azurion 5M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable.

    Product
    Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1661-2026·2026-04-08

    Philips Allura Xper FD10 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1674-2026·2026-04-08

    Philips Azurion 3 M15 X-ray may not start from foot switch

    Philips is recalling the Azurion 3 M15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1662-2026·2026-04-08

    Philips Allura Xper FD10/10 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD10/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1671-2026·2026-04-08

    Philips Allura Xper FD20/15 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20/15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/15; System Code: 722058;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1679-2026·2026-04-08

    Philips Azurion 5 M12 X-ray may not start from foot switch

    Philips is recalling the Azurion 5 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 5 M12; System Code: (1)722227, (2)722231;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1659-2026·2026-04-08

    Philips Allura Xper FD10C X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD10C because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD10C; System Code: 722001;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1676-2026·2026-04-08

    Philips Azurion 7 B20 X-ray may not start from foot switch

    Philips is recalling the Azurion 7 B20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1667-2026·2026-04-08

    Philips Allura Xper FD10 OR Table X-ray may not start reliably

    Philips is recalling the Allura Xper FD10 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1677-2026·2026-04-08

    Philips Azurion 7 M12 X-ray may not start from foot switch

    Philips is recalling the Azurion 7 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2026·2026-04-08

    Philips Azurion 3 M12 X-ray may not start from foot switch

    Philips is recalling the Azurion 3 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1675-2026·2026-04-08

    Philips Azurion 7 B12 X-ray may not start from foot switch

    Philips is recalling the Azurion 7 B12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1666-2026·2026-04-08

    Philips Allura Xper FD20 Biplane OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20 Biplane OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1668-2026·2026-04-08

    Philips Allura Xper FD20/10 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/10; System Code: 722029;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1669-2026·2026-04-08

    Philips Allura Xper FD20/20 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20/20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/20; System Code: 722038;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1660-2026·2026-04-08

    Philips Allura Xper FD10F X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD10F because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD10F; System Code: 722002;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1670-2026·2026-04-08

    Philips Allura Xper FD20/20 OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20/20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/20 OR Table; System Code: 722039;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1663-2026·2026-04-08

    Philips Allura Xper FD20 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1665-2026·2026-04-08

    Philips Allura Xper FD20 OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1672-2026·2026-04-08

    Philips Allura Xper FD20/15 OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20/15 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/15 OR Table; System Code: 722059;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1678-2026·2026-04-08

    Philips Azurion 7 M20 X-ray may not start from foot switch

    Philips has identified instances where X-ray imaging on the Azurion 7 M20 may not initiate, or may run intermittently, when the wired foot switch is used. 5,167 units are affected.

    Product
    Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1664-2026·2026-04-08

    Philips Allura Xper FD20 Biplane X-ray may not start reliably

    Philips is recalling the Allura Xper FD20 Biplane because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1680-2026·2026-04-08

    Philips Azurion 5 M20 X-ray may not start from foot switch

    Philips is recalling the Azurion 5 M20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);
    Category
    Medical Device
    Distribution
    Distributed nationwide