The Recall Desk

State

Arizona product recalls

72,968 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 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5226–5250 of 81349

  • SevereNHTSA·25E065000·2025-10-09

    Chrysler Recalls Mopar Gear Shift Control Cables Due to Park Function Loss

    Chrysler is recalling specific Mopar Gear Shift Control Cables that may detach from the transmission, preventing the vehicle from shifting into park and increasing the risk of a crash.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION:LEVER AND LINKAGE:FLOOR SHIFT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V677000·2025-10-09

    Braun Ambulances Recall 2023-2026 Models Due to Cruise Control Defect

    Braun Industries is recalling 2023-2026 ambulances because a damaged brake pedal switch may prevent cruise control from disengaging, increasing crash risk.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES LIBERTY TYPE I, EXPRESS PLUS TYPE I, CHIEF XL TYPE I, SELECT CHIEF XL I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V676000·2025-10-09

    Nissan and Chevrolet Vans Recalled for Fuel Pump Fuse Short Circuit Risk

    Nissan is recalling 2013-2021 NV200 and 2015-2018 Chevrolet City Express vans because a misrouted sensor harness may damage wires, causing a short circuit that could stall the engine.

    Product
    CHEVROLET — CHEVROLET, NISSAN CITY EXPRESS, NV200 TAXI, NV200, CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V680000·2025-10-09

    Genesis Supreme Recalls One Fifth Wheel Trailer Due to Fire Risk

    Genesis Supreme RV is recalling one 2024 Supreme 28IKS fifth wheel trailer because the air conditioner soft start device may overheat and cause a fire.

    Product
    GENESIS SUPREME — GENESIS SUPREME FIFTH WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2655-2025·2025-10-08

    BIOGRAPH One scanner recalled over ice blockage in magnet venting system

    Siemens is recalling one BIOGRAPH One (DE) system because an ice blockage in the magnet venting system could prevent helium escaping during a quench.

    Product
    BIOGRAPH One (DE). Model Number: 11689172.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2660-2025·2025-10-08

    MAGNETOM Skyra MRI systems recalled over ice blockage in venting system

    Siemens is recalling 586 MAGNETOM Skyra (DE) MRI systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.

    Product
    MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2612-2025·2025-10-08

    Reprocessed electrophysiology catheters recalled over residual particulates on patient surfaces

    Medline is recalling 7,913 reprocessed Inquiry Steerable Diagnostic Catheters because specific lots may carry small residual particulates on patient-contacting surfaces.

    Product
    Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during diagnostic electrophysiologic studies; Medline Item Numbers 81102RH 81104RH 81107RH 81174RH 81402RH 81404RH 81405RH 81472RH 81473RH 81474RH 81531RH 81532RH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2613-2025·2025-10-08

    Reprocessed cardiac imaging catheters recalled over residual particulates on device surfaces

    Medline is recalling 7,913 reprocessed ViewFlex Xtra ICE catheters because specific lots may carry small residual particulates on patient-contacting surfaces.

    Product
    Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and other devices within the heart. Medline Item Numbers D087031RH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2611-2025·2025-10-08

    Reprocessed cardiac mapping catheters recalled over residual particulates on device surfaces

    Medline is recalling 7,913 reprocessed Webster CS 10-electrode catheters because specific lots may carry small residual particulates on patient-contacting surfaces.

    Product
    Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological mapping of cardiac structures. Medline Item Numbers BD710DF282CRH BD710DF282RRH BD710FJ282CRH BD710FJ282RRH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2664-2025·2025-10-08

    MAGNETOM Verio MRI systems recalled over magnet venting ice blockage risk

    Siemens is recalling 154 MAGNETOM Verio MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    MAGNETOM Verio. Model Number: 10276755.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2658-2025·2025-10-08

    MAGNETOM Lumina MRI systems recalled over helium venting ice blockage risk

    Siemens is recalling 130 MAGNETOM Lumina (DE) MRI systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.

    Product
    MAGNETOM Lumina (DE). Model Number: 11344916.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2656-2025·2025-10-08

    MAGNETOM Cima.X systems recalled over ice blockage in helium venting system

    Siemens is recalling 22 MAGNETOM Cima.X (DE) systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.

    Product
    MAGNETOM Cima.X (DE). Model Number: 11647158.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2616-2025·2025-10-08

    Atlan A350 anesthesia workstations recalled after mechanical ventilation failures were reported

    Draeger is recalling 530 Atlan A350 anesthesia workstations that either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.

    Product
    Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates. The device can be used for mechanical vent
    Category
    Medical Device
    Distribution
    25 states