The Recall Desk

State

Arizona product recalls

73,509 recalls have nationwide distribution and so reach Arizona. 8,390 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total
8,390
Critical
1,313
Severe
2,047
Most recent
2026-10-14

Of the 8,390 recalls naming Arizona we have scored against our rubric, 1,313 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,047 (24%) are Severe.

Which agencies issued them

These figures cover only the 8,390 recalls whose distribution notice names Arizona specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25726–25750 of 81899

  • HighFDA (Devices)·Z-2440-2021·2021-09-15

    COPAN FLOQSwabs Recalled Over Sterilization Integrity Failure

    Copan Italia is recalling 3,029,400 COPAN FLOQSwabs distributed across the US due to sterilization integrity failures. The clinical sampling swabs cannot be guaranteed sterile due to data integrity issues at the contract sterilizer.

    Product
    COPAN FLOQSwabs, STERILE.EO, for drawing clinical samples. CE0123, for the following reference numbers REF:501CS01, Minitip, sterile Single Wrapped, Molded bp 80mm; REF: 20226, P/N 501CS01Q100, Minitip, Sterile, Single Wrapped, bp 60MM, BUNDLES OF 20 pcs; REF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2417-2021·2021-09-15

    Philips MRI System Tabletop May Not Fully Move in Manual Mode

    Philips Ingenia 3.0T-a MRI systems have an issue where the tabletop may not completely move in or out during manual operation. This could delay patient evacuation from the scanner bore and postpone medical treatment.

    Product
    Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2411-2021·2021-09-15

    MRI diagnostic device tabletop may not move completely in manual mode

    Philips Ingenia 1.5T MRI systems may have a mechanical defect where the tabletop fails to move fully in and out during manual operation, potentially delaying patient evacuation and treatment.

    Product
    Ingenia 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2426-2021·2021-09-15

    Medical diagnostic kit requires more frequent calibration than Instructions stated

    The Instructions for Use for Siemens' Atellica IM BR 27.29 Test Kit incorrectly specified a 10-day calibration interval instead of 3 days. The manufacturer has updated the instructions for all kit lots.

    Product
    Atellica IM BR 27.29 (BR) Assay 250 Test Kit (Reference)- in vitro diagnostic use in the quantitative serial determination of cancer antigen CA 27.29 in human serum and plasma (EDTA) using the Atellica IM Analyzer.- SMN: 11206236
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2415-2021·2021-09-15

    MRI System Tabletop May Fail to Move, Delaying Patient Evacuation

    Philips MRI systems (Model 781260) may have a tabletop malfunction in manual mode that prevents complete movement, potentially delaying patient evacuation and treatment.

    Product
    SmartPath to dStream for 1.5T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2439-2021·2021-09-15

    Solero Generator PG requires software service for startup error

    Angiodynamics is recalling 65 Solero Generator PG devices due to software Error 0001 that can occur during system startup. A software upgrade is required to reduce the incidence of this error.

    Product
    Solero Generator PG, Item No. H78712740000, Catalog No. 12740000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2436-2021·2021-09-15

    Solero MTA Generator requires software upgrade for startup error

    Angiodynamics is recalling specific refurbished Solero MTA Generators due to Error 0001, which occurs during system startup. A software upgrade is required to reduce the error's frequency.

    Product
    Solero Generator Refurbished US PG, Item No. H78712740000USD0, Catalog No. 12740000USD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2438-2021·2021-09-15

    Solero MTA Generator refurbished units require software servicing

    Eight refurbished Solero MTA Generator units require software upgrades to reduce startup errors occurring in specific serial numbers.

    Product
    Solero Generator Refurbished PG, Item No. H78712740000D0, Catalog No. 12740000D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2437-2021·2021-09-15

    Solero MTA Generator Requires Software Upgrade to Reduce Startup Error

    Angiodynamics is servicing specific Solero MTA Generator units to upgrade the software and reduce Error 0001 during startup. Affected units are identified by serial number.

    Product
    Solero Generator US PG, Item No. H78712740000US0, Catalog No. 12740000US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V711000·2021-09-14

    Ford Recalls 2021 Mustang Mach-E for Windshield Bonding Defect

    Ford is recalling 2021 Mustang Mach-E vehicles because the windshield may not be properly bonded. This defect could allow the windshield to detach during a crash, increasing injury risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V710000·2021-09-14

    Kaufman Equipment Trailer Recall for Defective Locking Mechanism

    Kaufman Trailers is recalling 2021 Equipment trailers because a defective locking mechanism may cause the trailer to detach from the vehicle, increasing crash risk.

    Product
    KAUFMAN — KAUFMAN EQUIPMENT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E086000·2021-09-14

    UFP Distribution Recalls WIC RV LPG Change Over Regulators

    UFP Distribution LLC is recalling specific WIC RV LPG change over regulators that may fail and increase propane pressure, posing a fire risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V709000·2021-09-13

    Altec Recalls 2021 Aerial Devices Due to Uncontrollable Boom Movement Risk

    Altec Industries is recalling 2021 AM50, 55, and 60E aerial devices because improperly machined cylinder rod threads may cause uncontrollable boom movement, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E085000·2021-09-13

    ZF Power Steering Pumps Recalled for Potential Loss of Assist

    ZF North America is recalling certain PS ED power steering pumps for Autocar and Spartan Fire vehicles due to a risk of losing power steering assist.

    Product
    STEERING:HYDRAULIC POWER ASSIST:PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V707000·2021-09-13

    2021 Audi E-Tron brake booster corrosion may disable braking systems

    Corrosion in the brake booster of certain 2021 Audi E-Tron vehicles may disable the Anti-Lock Brake System, Electronic Stability Control, and brake assist, increasing stopping distance and crash risk.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V708000·2021-09-13

    Keystone Hideout recreational vehicles recalled for propane regulator failure

    Certain 2020 Keystone Hideout recreational vehicles are recalled for faulty Winntec propane regulators that may fail and increase pressure, creating a fire risk in gas appliances. Dealers will replace the regulator free of charge.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN FUZION, BULLET, COLEMAN, KODIAK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V706000·2021-09-10

    2022 Nissan Pathfinder Hood Latch Bracket May Detach, Posing Crash Risk

    Nissan is recalling 2022 Pathfinder vehicles due to insufficient welds on the secondary hood latch bracket. The bracket may detach, allowing the hood to open if the primary latch fails, obstructing the driver's view and increasing crash risk.

    Product
    NISSAN — NISSAN PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V704000·2021-09-10

    Mercedes-Benz Recalls 2021 S 580 Vehicles for Fuel Pump Defect

    Mercedes-Benz is recalling 2021 S 580 vehicles because a loose fuel pump nozzle may cause engine stalls, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V718000·2021-09-10

    Fox Factory Recalls Tuscany Kits for 2019-2021 Silverado and Sierra Trucks

    Fox Factory is recalling 2,646 trucks equipped with specific Tuscany Kits due to a risk of front wheel separation from ball joint failure.

    Product
    TUSCANY MOTOR CO — TUSCANY MOTOR CO CHEVROLET SILVERADO 1500, GMC SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V702000·2021-09-10

    2022 GMC Acadia air bag system defect due to inactive safety module

    General Motors is recalling certain 2022 GMC Acadia vehicles with an unactivated sensing diagnostic module that prevents air bag deployment. The two affected units remain in dealer inventory.

    Product
    GMC — GMC ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21780·2021-09-09

    Teak shower benches recalled due to fall hazard and collapse risk

    Ivena teak shower benches sold at Costco can collapse during use, posing a fall hazard. Consumers have reported 81 incidents of collapse or breakage, including four injuries.

    Product
    Teak shower benches
    Category
    Consumer Product
    Distribution
    Distributed nationwide