The Recall Desk

State

Arizona product recalls

72,907 recalls have nationwide distribution and so reach Arizona. 8,381 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total
8,381
Critical
1,313
Severe
1,717
Most recent
2026-09-09

Of the 8,381 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 1,717 (20%) are Severe.

These figures cover only the 8,381 recalls whose distribution notice names Arizona specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

676–700 of 81288

  • HighNHTSA·26V484000·2026-07-27

    Jayco Recalls 2024-2026 Entegra Motorhomes Due to Brake Light Defect

    Jayco is recalling certain 2024-2026 Entegra motorhomes because exterior brake lights may stay on when brakes are not applied, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA ANTHEM, REATTA, CORNERSTONE RESERVE, REATTA XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V483000·2026-07-27

    Jayco Recalls 2026 Entegra Anthem Motorhomes for Incorrect Tire Label

    Jayco is recalling 2026 Entegra Anthem motorhomes because the vehicle certification label may list the wrong tire size, which could lead to installing incorrect replacement tires.

    Product
    ENTEGRA — ENTEGRA ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V480000·2026-07-24

    Yamaha Boat Trailer Recall Issued Due to Tongue Failure Risk

    Midwest Industries is recalling 2027 Yamaha boat trailers because the tongue may fail during towing, causing the trailer to detach and increasing crash risk.

    Product
    YAMAHA — YAMAHA BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V481000·2026-07-24

    Mercedes-Benz Recalls Various Models Due to Driver's Door Lock Defect

    Mercedes-Benz USA, LLC is recalling certain 2020-2026 Mercedes-Benz vehicles because a faulty door lock micro-switch may cause the vehicle to roll away.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLA 35, AMG A35, GLB 250 4MATIC, GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V482000·2026-07-24

    Frontrunner Recalls 2025 Transit Buses Due to Wheelchair Retract Defect

    Frontrunner is recalling 2025 transit buses because wheelchair retractors may fail to lock, increasing injury risk. Owners will be notified to have parts replaced.

    Product
    FRONTRUNNER — FRONTRUNNER FRONTRUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26634·2026-07-23

    12-Drawer Fabric Dressers Recalled for Tip-Over and Entrapment Hazards

    Romorgniz 12-Drawer Fabric Dressers sold on Amazon pose tip-over and entrapment risks to children if not anchored to the wall. About 10,040 units are affected.

    Product
    Romorgniz 12-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26636·2026-07-23

    Sviyatp Pool Drain Covers Recalled for Entrapment and Drowning Risk

    About 670 Sviyatp pool drain covers sold online violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using affected pools immediately and contact Sviyatp for a refund.

    Product
    Sviyatp Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V478000·2026-07-23

    BMW S 1000 RR Motorcycles Recalled Due to Potential Engine Stall Risk

    BMW is recalling certain 2020-2026 S 1000 RR motorcycles because vibration may cause ignition lock failure, leading to engine stalls or electrical system failures.

    Product
    BMW — BMW S 1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26633·2026-07-23

    EnHomee 9-Drawer Fabric Dressers Recalled for Tip-Over and Entrapment Hazard

    EnHomee 9-Drawer Fabric Dressers sold on Walmart.com pose a risk of serious injury or death from tip-over and entrapment if not anchored to the wall. About 16,809 units are affected.

    Product
    EnHomee 9-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E048000·2026-07-23

    K&N and Spectre Fuel Filters Recalled for O-Ring Disintegration

    K&N Engineering is recalling specific K&N and Spectre replacement fuel filters because the O-ring may disintegrate, causing leaks or clogs.

    Product
    FUEL SYSTEM, OTHER:FUEL FILTER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26638·2026-07-23

    CuddleCubs Creations Teething Toy Sets Recalled for Choking Risk

    CuddleCubs Creations Baby Highchair Teething Toy Sets are recalled due to pull-string teething toys that violate mandatory toy safety standards. The silicone strings can lodge in a child's throat, creating a risk of choking and respiratory distress.

    Product
    CuddleCubs Creations Baby Highchair Teething Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V476000·2026-07-23

    Forest River Recalls 2027 Travel Trailers with Incorrect Water Tank Labels

    Forest River is recalling 2027 travel trailers because the Federal Placard may list an incorrect fresh water tank capacity, which could lead to vehicle overloading.

    Product
    FOREST RIVER — FOREST RIVER SABRE, NO BOUNDARIES, IBEX, SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26639·2026-07-23

    Personalized Baby Bibs and Stroller Bags Recalled for Choking Hazard

    Peony Design has recalled personalized baby bibs and stroller bags sold online because snaps can detach, posing a choking risk to young children. The company is offering refunds.

    Product
    Personalized Baby Bibs and Stroller Bags
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26637·2026-07-23

    OeyUoc Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    OeyUoc white pool drain covers sold on Amazon violate safety standards and pose entrapment and drowning risks. About 404 units have been recalled; consumers should stop using them immediately.

    Product
    OeyUoc Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26635·2026-07-23

    Sili Factory Pull String Teething Toys recalled for choking hazard risk

    Aojieni Silicone is recalling about 5,918 Sili Factory Pull String Teething Toys because the silicone strings violate toy safety standards and can lodge in a child's throat, posing a serious choking risk.

    Product
    Sili Factory Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2704-2026·2026-07-22

    Transvenous Pacing Electrode Tray with Bipolar Balloon Pacing Electrode Recalled

    Argon Medical Devices is recalling Transvenous Pacing Electrode Trays with Bipolar Balloon Pacing Electrode 5F because kits containing Lidocaine HCL Injection USP did not meet sterility release criteria.

    Product
    Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2686-2026·2026-07-22

    ABIOMED Impella CP Introducer Kit 14 Fr potentially defective sheath

    Abiomed, Inc. is recalling ABIOMED Impella CP Introducer Kit 14 Fr units worldwide due to potential introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable.

    Product
    ABIOMED Impella CP Introducer Kit 14 Fr, 25 cm, Pump Set Code 0052-0039, containing Kit, 14Fr Introducer, 25cm, Long Taper, Introducer Product Code 0052-3053. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0690-2026·2026-07-22

    ChloraPrep One-Step Applicators Recalled for Potential Packaging Seal Defects

    CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) applicators nationwide because affected units may have open or incomplete seals on the packaging, which could compromise sterility assurance.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2720-2026·2026-07-22

    Olympus Ellik Evacuator Recalled for Inadequate Sterilization Risk

    Olympus Corporation of the Americas is recalling the Olympus Ellik Evacuator (Model 194) worldwide because certain sterilization parameters in the instructions may not render the device adequately sterile.

    Product
    Olympus Ellik Evacuator Includes Glass Body, Male Connecting Tubing & Latex Bulb. Model Number: 194.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2708-2026·2026-07-22

    Arterial Line Kit with Lidocaine HCL Injection Fails Sterility Testing

    Argon Medical Devices is recalling an Arterial Line Kit containing Lidocaine HCL Injection USP because the kits do not meet sterility release criteria, creating a risk of infection from non-sterile medical injection.

    Product
    Arterial Line Kit 20ga x 6, REF: 400115A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2688-2026·2026-07-22

    Abiomed Impella 5.5 SmartAssist S2 heart pump introducer sheath leakage risk

    Abiomed is recalling Impella 5.5 SmartAssist S2 heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines that may not be visible to users.

    Product
    ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1000459, 1000460; containing Introducer Product Code 0052-3006-JP. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide