The Recall Desk

State

Arizona product recalls

73,486 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 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24276–24300 of 81876

  • ModerateFDA (Drugs)·D-0364-2022·2022-01-19

    The Natural Dentist Mouthwash Label Mix-Up Recall

    The Natural Dentist Healthy Balance Peppermint Sage mouthwash (16.9 FL OZ, Lot 2091A) has been recalled due to a back label mix-up. The label incorrectly identifies the active ingredient as Menthol with the wrong UPC code instead of the correct Peppermint Oil and Sage Oil.

    Product
    The Natural Dentist Healthy Balance Peppermint Sage, Menthol 0.12%, 16.9 FL OZ (500 mL) bottles, Manufactured for Revive Personal Products Company, Madison, NJ 07940, UPC 7 14132 00071 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0365-2022·2022-01-19

    Carbamazepine tablets recalled for failed dissolution specifications

    Torrent Pharma Inc. is recalling Carbamazepine 200 mg tablets nationwide because they failed to meet dissolution specifications, which means the tablets may not release the medication properly in the body.

    Product
    CARBAMAZEPINE — CARBAMAZEPINE (CARBAMAZEPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0482-2022·2022-01-19

    Instavac Portable Suction Pumps Recalled for Premature Device Failures

    Ohio Medical Corporation is recalling Instavac Portable Suction Pumps (models 757000, 756000, and replacement pump part #AI5511) due to an increase in premature device failures. Affected units were distributed nationwide.

    Product
    Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac replacement pumps, part #AI5511, a component of model numbers 756000 and 757000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0368-2022·2022-01-19

    Oxycodone Hydrochloride Oral Solution recalled for missing label

    Akorn, Inc. is recalling Oxycodone Hydrochloride Oral Solution 5 mg per 5 mL distributed nationwide due to missing label.

    Product
    Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg/mL), 500 mL bottle, Rx only, Manufactured by: Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 --- NDC 50383-961-34
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0367-2022·2022-01-19

    Morphine Sulfate Oral Solution 20 mg/mL recalled for missing label

    Akorn, Inc. is recalling Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) in 30 mL bottles nationwide due to missing labeling on approximately 10,836 bottles.

    Product
    Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles, Rx only, Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 -- NDC 50383-965-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V016000·2022-01-18

    2022 Peterbilt 579 chassis step bolts may loosen and cause injury

    Bolts securing the chassis fairing step assembly on certain 2022 Peterbilt 579 vehicles may loosen and fracture. This can cause the step to move unexpectedly while entering or exiting the cab, increasing the risk of injury.

    Product
    PETERBILT — PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V015000·2022-01-17

    2022 Keystone Alpine RV Exterior Ladder May Detach from Rear Wall

    Keystone RV Company is recalling certain 2022 Alpine and Avalanche vehicles due to improperly secured exterior ladders that may detach while in use, creating a risk of injury.

    Product
    KEYSTONE — KEYSTONE ALPINE, AVALANCHE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E002000·2022-01-14

    Tenneco Recalls Aftermarket Ball Joints for Toyota Sequoia and Tundra

    Tenneco Automotive is recalling aftermarket ball joints for 2004-2007 Toyota Sequoia and 2004-2006 Toyota Tundra vehicles due to potential premature failure.

    Product
    TOYOTA — TOYOTA SEQUOIA, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V014000·2022-01-14

    KTM Recalls 2022 Husqvarna Motorcycles for Brake Pad Retaining Clip Defect

    KTM is recalling 2022 Husqvarna FE 350S and FE 501S motorcycles because incorrectly mounted front brake pad retaining clips may cause pads to detach, reducing braking performance.

    Product
    HUSQVARNA — HUSQVARNA FE 350S, FE 501S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V013000·2022-01-14

    2021 Ford Diesel Trucks Fuel Filter Cap Defect Fire Risk

    Ford is recalling certain 2021 diesel trucks due to a void in the secondary fuel filter cap that may leak fuel, posing a fire risk. Dealers will replace the fuel filters free of charge.

    Product
    FORD — FORD F-550 SD, F-450 SD, F-650, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V012000·2022-01-14

    2022 Forest River Cherokee toy hauler tires may be incorrectly specified on placard

    Forest River is recalling certain 2022 Cherokee toy haulers because the Tire and Loading Information placard may show incorrect rim specifications, potentially causing improper tire installation and crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V011000·2022-01-13

    Ford Recalls Fusion, MKZ, and Mustang for Brake Pedal Bumper Defect

    Ford is recalling 2014-2015 Fusion, Lincoln MKZ, and 2015 Mustang vehicles because brake pedal bumpers may corrode and separate, potentially causing brake light confusion or rollaway risks.

    Product
    FORD — FORD, LINCOLN FUSION, MKZ, MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V010000·2022-01-13

    Seagrave Recalls 2011-2021 Firetrucks Due to Cracking Crossmember Plate

    Seagrave is recalling 2011-2021 Marauder and Capitol firetrucks because a crossmember mounting plate may crack, potentially distracting the driver and increasing crash risk.

    Product
    SEAGRAVE — SEAGRAVE MARAUDER, CAPITAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22717·2022-01-13

    Textron E-Z-GO Freedom RXV Personal Transportation Vehicles Recalled Due to Fall Hazards

    Textron Specialized Vehicles is recalling about 280 E-Z-GO Freedom RXV personal transportation vehicles with rear-facing seats because the rear seat structure can fail and tilt unexpectedly, creating a fall and injury hazard. Consumers should stop using the rear-facing seat and contact Textron for a free repair.

    Product
    E-Z-GO Freedom RXV with Rear Facing Seat Personal Transportation Vehicles (PTV)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0363-2022·2022-01-12

    Nature's Own Honey Wheat Bread recalled for undeclared milk

    Flowers Foods is recalling Nature's Own Honey Wheat Bread due to undeclared milk, which poses a risk to consumers with milk allergies. The product was distributed in Arizona, California, Colorado, New Mexico, Nevada, and Wyoming.

    Product
    Nature's Own Honey Wheat Bread, NET WT 20 oz (1LB 4 OZ) 567g, DISTRIBUTED BY FLOWERS BAKERIES, LLC THOMASVILLE, GA 31757 Single loaf UPC 0 72250 03706 8 & Double pack UPC 0 72250 00539 5
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0445-2022·2022-01-12

    Power wheelchairs with LiNX Gyro module recalled for deceleration control failure

    Invacare power wheelchairs with LiNX Gyro firmware 6.1.2 may decelerate more aggressively than programmed, risking user injury due to an incorrect deceleration profile.

    Product
    Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: TDX SP2: TDXSP2, TDXSP2-CG, TDXSP2X-CG, TDXSP2-MCG, TDXSP2X-MCG, TDXSP2V, TDXSP2V-HD, TDXSP2HD, TDXSP2HD-CG, TDXSP2HD-MCG
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22052·2022-01-12

    EGL and ACE Youth All-Terrain Vehicles Recalled for Safety Standard Violations

    EGL Motor is recalling about 2,900 EGL and ACE branded youth ATVs (models MADIX 125 and D110) because they fail federal safety standards, allowing children to exceed safe speeds and creating laceration and crash hazards.

    Product
    EGL and ACE Branded Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0457-2022·2022-01-12

    Medical Device Kit Poses Risk of Sample Leakage and Lab Contamination

    DiaSorin Molecular's Simplexa Direct Amplification Disc Kit is recalled due to risk of leakage when used multiple times, which may cause cross-contamination in laboratory settings if not properly cleaned.

    Product
    Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Food)·F-0365-2022·2022-01-12

    Trader Joe's Soycutash recalled for Listeria contamination

    Trader Joe's Soycutash (Item #99319), a frozen mix of sweet corn, shelled edamame, and red bell peppers, is being recalled because it may be contaminated with Listeria monocytogenes. The recall affects products distributed in Arizona, California, Nevada, and Utah.

    Product
    Trader Joe's Soycutash, Item # 99319. A mix of Sweet Corn, Shelled Edamame, and Red Bell Peppers. Net Wt. 16 oz. (1 lb.) 454g. Keep Frozen. UPC 0099-3197. Dist & Sold Exclusively By: Trader Joe's Monrovia, CA 91016
    Category
    Food
    Distribution
    4 states
  • HighCPSC·22053·2022-01-12

    Children's Robes Recalled for Flammability Standards Violation

    About 3,500 children's robes made by HulovoX fail federal flammability standards for sleepwear and pose a burn injury risk. The robes were sold online through Amazon.com from January to May 2021 for about $30 each.

    Product
    Children's Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0461-2022·2022-01-12

    Alinity m System Software Issue Affects Maintenance and Diagnostics Procedures

    Abbott Molecular is recalling 742 Alinity m System units worldwide due to a software issue that prevents Field Service Engineers from properly completing maintenance and diagnostics procedures.

    Product
    Alinity m System, Part No. 08N53-002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0449-2022·2022-01-12

    Clinical Chemistry Analyzer Software Flaw May Cause Inaccurate Test Results

    Siemens is recalling Atellica CH 930 clinical chemistry analyzers with software v1.25.1 or lower. Two software defects could cause inaccurate test results: test parameters may revert to defaults, or the analyzer may use expired reagents.

    Product
    Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An automated, clinical chemistry analyzer designed to perform in vitro diagnostic tests on clinical specimens. Siemens Material Number (SMN): 11067000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0446-2022·2022-01-12

    Invacare AVIVA FX power wheelchair LiNX Gyro deceleration malfunction

    Some Invacare AVIVA FX power wheelchairs with LiNX Gyro firmware 6.1.2 may decelerate more aggressively than programmed, creating injury risk.

    Product
    Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: IFX-20R, IFX-20SP, IFX-20MP, IFX-20C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0458-2022·2022-01-12

    UROMEDICA Implantation Instrument Sheath May Damage ProACT Implants

    Uromedica is recalling nonsterile implantation instrument sheaths (Lot UM00794 and UM00817) because the U-channel sheaths may damage ProACT implant devices during implantation procedures. Affected devices were distributed nationwide.

    Product
    UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide