The Recall Desk

State

Arizona product recalls

73,495 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.

These figures cover only the 8,390 recalls whose distribution notice names Arizona specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24976–25000 of 81885

  • ModerateFDA (Drugs)·D-0088-2022·2021-11-10

    Irbesartan 300 mg tablets recalled for impurity in active ingredient

    Lupin Pharmaceuticals is recalling Irbesartan 300 mg tablets due to the detection of N-nitrosoirbesartan impurity in the active pharmaceutical ingredient. The recall affects approximately 119,544 bottles distributed nationally.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0201-2022·2021-11-10

    Medtronic Neuromodulation Clinician Programmer Application Software Anomaly Recall

    Medtronic recalled the Clinician Programmer Application (CPA) model A610 due to a potential software anomaly. Affected versions 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081 have been distributed worldwide. No illnesses or injuries have been reported.

    Product
    Clinician Programmer Application (CPA) model A610 Clinician Software Application
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0081-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Excipient Specification Failure

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin 10 mg/10 mg tablets nationwide because the product was manufactured using an excipient that failed to meet conductivity specifications.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0089-2022·2021-11-10

    Starbucks Doubleshot Espresso canned coffee recalled for sealing defect

    PepsiCo is recalling Starbucks Doubleshot Espresso and Espresso & Cream canned coffee products because inadequate sealing may cause premature spoilage.

    Product
    Starbucks Doubleshot Espresso, Espresso & Cream, 6.5 FL OZ UPC 012000001772
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0091-2022·2021-11-10

    Starbucks Doubleshot Espresso Canned Coffee Recall for Sealing Defect

    PepsiCo is recalling Starbucks Doubleshot Espresso and Espresso & Salted Caramel Cream canned coffee products due to inadequate sealing that may lead to premature spoilage.

    Product
    Starbucks Doubleshot Espresso, Espresso & Salted Caramel Cream, 6.5 FL OZ UPC 012000007293
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V868000·2021-11-09

    2021 Tesla Model X and Model S driver air bags may tear during deployment

    Tesla is recalling certain 2021 Model X and Model S vehicles because the driver's air bag cushion may tear during deployment, potentially failing to protect occupants in a crash. Tesla will replace the air bag free of charge.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V867000·2021-11-08

    Hazard Lights Disabled When Ignition Off in Autocar Xpeditor Vehicles

    Autocar is recalling 2019-2022 Xpeditor vehicles because the hazard lights will not function with the ignition turned off. This violates federal safety standards and could increase crash risk in hazard situations.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V861000·2021-11-05

    Isuzu and Chevrolet Trucks Recalled for Steering Knuckle Bolt Issue

    Isuzu is recalling 2018-2021 FTR and Chevrolet 6500XD trucks because a steering bolt may loosen, causing difficulty steering and increased crash risk.

    Product
    ISUZU — ISUZU, CHEVROLET FTR, 6500XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V864000·2021-11-05

    Steering shaft defect in 2021-2022 Western Star 49X commercial trucks

    2021-2022 Western Star 49X trucks may have improperly installed steering shafts that can separate, causing loss of steering control. Daimler will inspect and repair affected vehicles free of charge.

    Product
    WESTERN STAR — WESTERN STAR 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V680000·2021-11-05

    Tiffin Motorhomes Recall: Sofa Seat Belts May Be Improperly Installed

    Tiffin Motorhomes is recalling certain 2018–2022 recreational vehicles with sofa seat belts that may not be correctly installed. Unsecured passengers face increased injury risk in a crash.

    Product
    TIFFIN — TIFFIN ALLEGRO, ALLEGRO RED, PHAETON, ZEPHYR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V863000·2021-11-05

    Cottrell Recalls 2-Car Carriers Due to Missing Rear Reflectors

    Cottrell is recalling 2019-2022 2-Car Carriers because four side-rear reflex reflectors are missing, which reduces visibility and increases crash risk.

    Product
    COTTRELL — COTTRELL 2-CAR CARRIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V860000·2021-11-05

    2021 Mercedes-Benz GLB250 and AMG GLB35 airbag mounting defect

    Mercedes-Benz is recalling certain 2021 GLB250 and AMG GLB35 vehicles because the driver-side window airbag may not be properly mounted to the A-pillar, which could prevent proper deployment during a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLB35, GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V858000·2021-11-04

    Volvo Recalls 2021 VNL Trucks Due to Power Steering Pump Defect

    Volvo Trucks North America is recalling 2021 VNL vehicles because a machining defect in the power steering pump may cause a loss of steering assist, increasing crash risk.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22705·2021-11-04

    Kubota RTV-X1100C Utility Vehicles Floor Mat Interference Recall

    Kubota is recalling about 48,875 RTV-X1100C utility vehicles from model years 2013 through 2021 because floor mats can warp or degrade and interfere with the throttle pedal, creating crash and injury risks.

    Product
    Kubota RTV-X1100C Model Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V857000·2021-11-04

    Tracker Recalls 2022 Ranger Trail Boat Trailers Due to Fender Spacing

    Tracker Marine is recalling 2022 Ranger Trail boat trailers because improperly spaced fenders may contact tires, causing premature wear and potential tire failure.

    Product
    RANGER TRAIL — RANGER TRAIL BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22706·2021-11-04

    Backyard Play Systems Outdoor Playsets Recalled for Entrapment Hazard

    Backyard Play Systems is recalling four outdoor playset models due to an entrapment hazard in the wooden roof design. Children can become trapped in gaps between the roof structure and gable decoration.

    Product
    Turbo Racer, Cloud Racer, Captain's Fort and Fort Highlander Outdoor Playsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0118-2022·2021-11-03

    Surgical Brain Guidance System Recalled for Inaccurate Electrode Placement

    ROSA One 3.1 surgical guidance system recalled due to a software anomaly causing inaccurate electrode placement during brain and spine surgery. Manufacturer received 3 complaints related to the issue.

    Product
    ROSA One 3.1 Brain application The device is intended for the spatial positioning and orientation of instruments holders or tool guides to be used by trained surgeons to guide standard surgical instruments during brain and spine surgeries.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0046-2022·2021-11-03

    Test Cyp Injectable Drug Recalled for Sterility Assurance Defects

    First Royal Care Compounding Pharmacy is recalling Test Cyp 50mg/ml in ethyl oleate oil due to FDA inspection findings that raised concerns about sterility assurance. About 494 patients in seven states received prescriptions for the affected product.

    Product
    TEST CYP 50MG/ML IN ETHYL OLEATE OIL, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0053-2022·2021-11-03

    Acetylcysteine 10% ophthalmic solution recalled for sterility assurance concerns

    Red Mountain Compounding Pharmacy is recalling Acetylcysteine 10% ophthalmic solution due to lack of sterility assurance identified during an FDA inspection. Approximately 494 patients received prescriptions for the product across seven states.

    Product
    ACETYLCYSTEINE 10% OPTH SOLN, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0030-2022·2021-11-03

    Levocarnitine 100mg/mL Solution Recall Due to Sterility Assurance

    Red Mountain Compounding Pharmacy is recalling Levocarnitine 100mg/mL solution for injection because FDA inspection found concerns about the product's sterility assurance. The product was distributed to patients in seven states.

    Product
    LEVOCARNITINE 100MG/ML MDV SOLN, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0037-2022·2021-11-03

    Estradiol Valerate Injection Recalled for Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling Estradiol Valerate 5mg/mL injectable medication due to FDA inspection findings of inadequate sterility assurance. The product was distributed to approximately 494 patients across seven states.

    Product
    ESTRADIOL VALERATE 5MG/ML MDV INJ, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states