The Recall Desk

Hazard

Structural Failure recalls

2,056 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,056
Critical
10
Severe
1,049
Most recent
2026-09-17

Of the 2,056 structural failure recalls we have scored against our rubric, 10 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (51%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all structural 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.

651–675 of 2056

  • SevereFDA (Devices)·Z-0544-2019·2018-12-12

    Philips Brilliance 40 CT Systems Recalled for Gantry Cover Separation Risk

    Philips is recalling 6,343 Brilliance 40 CT systems nationwide due to a potential fiberglass resin separation that could cause the gantry front cover to fall.

    Product
    Brilliance 40, Model 728235 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and displa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0545-2019·2018-12-12

    Philips Brilliance 16 Slice CT Scanner Recalled for Gantry Cover Separation Risk

    Philips Medical Systems is recalling 6,343 Brilliance 16 Slice CT scanners nationwide due to a potential fiberglass resin separation that could cause the gantry front cover to fall.

    Product
    Brilliance 16 Slice (Power), Model 728240 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0548-2019·2018-12-12

    Philips Brilliance 6 Slice CT Scanner Recalled for Gantry Cover Separation Risk

    Philips Medical Systems is recalling Brilliance 6 Slice CT scanners because fiberglass resin may separate, causing the gantry front cover to fail or fall.

    Product
    Brilliance 6 Slice (Air), Model 728256 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0546-2019·2018-12-12

    Philips Brilliance 16 Slice CT Scanner Recall for Cover Separation

    Philips is recalling Brilliance 16 Slice CT scanners because fiberglass resin may separate, causing the gantry front cover to fail or fall.

    Product
    Brilliance 16 Slice (Air), Model 728246 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analyst
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0547-2019·2018-12-12

    Philips Brilliance 10 Slice CT Scanner Recalled for Gantry Cover Failure Risk

    Philips is recalling Brilliance 10 Slice CT scanners because fiberglass resin may separate, causing the gantry front cover and metal support to fail or fall.

    Product
    Brilliance 10 Slice (Air), Model 728251 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analyst
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0543-2019·2018-12-12

    Philips Brilliance 64 CT Scanner Recall for Gantry Cover Separation Risk

    Philips Medical Systems is recalling Brilliance 64 CT scanners due to a potential fiberglass resin separation that could cause the gantry front cover to fail and fall.

    Product
    Brilliance 64, Model 728231 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and displ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V847000·2018-11-28

    Altec Recalls 2017 Aerial Devices Due to Pedestal Fastener Defect

    Altec is recalling 2017 AT37, AT41, and AT48 aerial devices because loose or missing fasteners may cause the pedestal to separate, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0488-2019·2018-11-28

    Sedecal NOVA FA DR System Recalled for Potential Cable Failure

    Sedecal S.A. is recalling 145 NOVA FA DR diagnostic radiography systems because installation or maintenance issues could cause support cables to break, leading to equipment falling.

    Product
    Sedecal NOVA FA DR System. for diagnostic radiography.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0426-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.

    Product
    OviTex 1S Reinforced BioScaffold 18x22cm, Part Number F10256-1822G
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0417-2019·2018-11-21

    AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex Reinforced BioScaffold 10x12cm devices because the suture material degraded, causing them to fail burst specifications after 18 months.

    Product
    OviTex Reinforced BioScaffold 10x12cm, Part Number F10254-1012G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0420-2019·2018-11-21

    AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex Reinforced BioScaffold 20x20cm devices because the suture material degraded, causing them to fail burst specifications after 18 months.

    Product
    OviTex Reinforced BioScaffold 20x20cm, Part Number F10254-2020G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0421-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold 4x8cm devices because the PGA suture material degraded, causing the devices to fail burst specifications.

    Product
    OviTex 1S Reinforced BioScaffold 4x8cm, Part Number F10256-0408G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0430-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material may degrade, causing them to fail burst specifications.

    Product
    OviTex 2S Reinforced BioScaffold 10x20cm, Part Number F10258-1020G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0435-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications after 18 months.

    Product
    OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0432-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.

    Product
    OviTex 2S Reinforced BioScaffold 18x22cm, Part Number F10258-1822G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0427-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.

    Product
    OviTex 1S Reinforced BioScaffold 20x20cm, Part Number F10256-2020G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0431-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications after 18 months.

    Product
    OviTex 2S Reinforced BioScaffold 16x20cm, Part Number F10258-1620G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0418-2019·2018-11-21

    AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.

    Product
    OviTex Reinforced BioScaffold 10x20cm, Part Number F10254-1020G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0422-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Devices

    AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.

    Product
    OviTex 1S Reinforced BioScaffold 6x10cm, Part Number F10256-0610G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0419-2019·2018-11-21

    AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex Reinforced BioScaffold 16x20cm devices because the suture material degraded, causing them to fail burst specifications after 18 months.

    Product
    OviTex Reinforced BioScaffold 16x20cm, Part Number F10254-1620G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0429-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold 10x12cm devices because the suture material degraded, causing them to fail burst specifications.

    Product
    OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0423-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.

    Product
    OviTex 1S Reinforced BioScaffold 10x12cm, Part Number F10256-1012G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0416-2019·2018-11-21

    AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices

    AROA Biosurgery is recalling OviTex Reinforced BioScaffold mesh devices because the suture material degraded, causing some units to fail burst specifications.

    Product
    OviTex Reinforced BioScaffold 6x10cm, Part Number F10254-0610G
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0428-2019·2018-11-21

    AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Devices

    AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.

    Product
    OviTex 2S Reinforced BioScaffold 6x10cm, Part Number F10258-0610G
    Category
    Medical Device
    Distribution
    8 states