The Recall Desk

State

Arizona product recalls

73,596 recalls have nationwide distribution and so reach Arizona. 8,391 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total
8,391
Critical
1,311
Severe
2,049
Most recent
2026-10-21

Of the 8,391 recalls naming Arizona we have scored against our rubric, 1,311 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,049 (24%) are Severe.

Which agencies issued them

These figures cover only the 8,391 recalls whose distribution notice names Arizona specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29201–29225 of 81987

  • ModerateFDA (Devices)·Z-0469-2021·2020-11-25

    Siemens Artis X-Ray Systems Recalled for Overvoltage Protection Defect

    Siemens is recalling 26 Artis X-ray systems worldwide because incorrect diodes may fail to protect against overvoltage, potentially causing system malfunction.

    Product
    Artis zee floor, Artis Q ceiling, Artis Q.zen ceiling. Image-Intensified Fluoroscopic X-Ray System. Material numbers 10848281, 10848354, 10094135, 10848354 - Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0101-2021·2020-11-25

    Hikma Recalls Sodium Chloride Injection Vials Due to pH Failures

    Hikma Pharmaceuticals is recalling specific lots of Sodium Chloride Injection USP 0.9% 2 mL vials because they failed pH specifications.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0459-2021·2020-11-25

    Exactech Equinoxe Cage Glenoid Posterior Augment Recalled for Mislabeling

    Exactech, Inc. is recalling 69 Equinoxe Cage Glenoid, Posterior Augment, Left, Medium devices because they may be mislabeled.

    Product
    Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-0474-2021·2020-11-25

    Siemens Atellica IM 1600 Analyzer Recalled for Custom Settings Reset

    Siemens Healthcare Diagnostics is recalling Atellica IM 1600 Analyzers because scanning a new kit lot may reset custom settings to defaults.

    Product
    Atellica IM 1600 Analyzer - Product Usage: automated, immunoassay analyzers designed to perform in vitro diagnostic tests on clinical specimens. Siemens Material Number (SMN): 11066000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0450-2021·2020-11-25

    Ortho Recalls VITROS SARS-CoV-2 IgG Calibrators Due to Elevated Signal Values

    Ortho Clinical Diagnostics is recalling specific lots of VITROS SARS-CoV-2 IgG Calibrators because they produced elevated signal values. The recall also includes one lot of IgG Controls with decreased signal.

    Product
    VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage: In-Vitro Diagnostic (EUA) an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. Emergency use of this test is limited to authorized…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0440-2021·2020-11-25

    Inova Lasers Recalls Class IV New Era Medical Laser Devices

    Inova Lasers LLC is recalling eight Class IV New Era medical laser devices because they failed to comply with Electronic Product Radiation Control regulations.

    Product
    Class IV New Era medical laser device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0460-2021·2020-11-25

    Exactech Equinoxe Cage Glenoid Posterior Augment Recalled for Mislabeling

    Exactech is recalling 40 Equinoxe Cage Glenoid, Posterior Augment, Right, Medium devices due to potential mislabeling. The devices were distributed to US and international consignees.

    Product
    Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium
    Category
    Medical Device
    Distribution
    21 states
  • LowFDA (Devices)·Z-0458-2021·2020-11-25

    Steris Olympus Leak Test Adapter Recalled for Cleaning Solution Intrusion Risk

    Steris Corporation is recalling Olympus Leak Test Adapters used with Acu-sInQ systems due to a potential for cleaning solution to intrude into endoscopes.

    Product
    Olympus Leak Test Adapter used with Acu-sInQ Complete Endoscope Cleaning Aid Systems-intended to assist manual flexible endoscope cleaning Part number: 0600818OKN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0471-2021·2020-11-25

    Ortho VITROS Chemistry Performance Verifier II Recalled for Product Instability

    Ortho Clinical Diagnostics is recalling VITROS Chemistry Products Performance Verifier II due to product instability that causes biased ALKP values.

    Product
    VITROS Chemistry Products Performance Verifier II-For in vitro diagnostic use only.VITROS Chemistry Products Performance Verifier is an assayed control used to monitor performance on VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and the VITROS 5600/XT 7600 Integrated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0401-2021·2020-11-25

    Merz Recalls COAPTITE Injectable Implant Due to Documentation Mismatch

    Merz North America is recalling 2,051 units of COAPTITE Injectable Implant because the Instructions for Use do not match post-approval study data.

    Product
    COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns in diameter of calcium hydroxylapatite (CaHA), suspended in aqueous based gel carrier. Gel carrier is composed of sodium carboxymethylcellulose, sterile water…
    Category
    Medical Device
    Distribution
    48 states
  • LowFDA (Devices)·Z-0470-2021·2020-11-25

    Micro-Tech Elastic Traction Device Recalled for Regulatory Classification Issues

    Micro-Tech USA is recalling Elastic Traction Devices because they are not appropriately classified as Class I and require 510(k) clearance.

    Product
    Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use in flexible Endoscopy to provide retraction to assist in tissue resection, exposure, and removal of tissue within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V730000·2020-11-24

    Ford Recalls 2020 Explorers Due to Fuel Tank Weld Defect

    Ford is recalling 2020 Explorers with 2.3L engines because an incomplete weld on the fuel tank inlet check valve could cause a fuel leak and fire during a crash.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V729000·2020-11-24

    Mercedes-Benz Metris Recalled for Potential Brake Line Fitting Defects

    Daimler Vans USA is recalling 2019-2020 right-hand drive Mercedes-Benz Metris vehicles because brake line fittings may be incorrectly installed, risking fluid leaks and reduced braking performance.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21710·2020-11-24

    Any Volume Recalls Bicycle Helmets Due to Head Injury Risk

    Any Volume is recalling about 660 adult bicycle helmets sold on eBay because they do not comply with U.S. safety standards, posing a risk of head injury.

    Product
    Bicycle Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20E088000·2020-11-24

    Weldon i4G Vivtech Control Panels Recalled for Electrical Defect

    Weldon is recalling i4G Vivtech control panels because an electrical defect may cause the display to stop working, potentially delaying emergency services.

    Product
    ELECTRICAL SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V727000·2020-11-23

    Multiple recreational vehicle models recalled for cooking stove gas leak

    Forest River and Coachmen recreational vehicles with Dometic 3-burner cooking stoves may experience gas leaks from overtightened saddle valve bolts, creating a fire hazard. Owners should contact dealers for a free remedy kit.

    Product
    COACHMEN — COACHMEN, FOREST RIVER, DYNAMAX CROSS TREK, FREELANDER, LEPRECHAUN, MIRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V728000·2020-11-23

    Rosenbauer Aerial Vehicles Recalled for Power Take-Off Defect

    Rosenbauer America is recalling 2018-2020 Aerial vehicles because the power take-off may disengage, causing the aerial device to become inoperable.

    Product
    ROSENBAUER — ROSENBAUER AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V721000·2020-11-20

    Isuzu and Chevrolet Recall 2020 Trucks for Wiring Chafe Risk

    Isuzu and Chevrolet are recalling 2020 NPR-HD and 4500 Crew Cab trucks because a chafing wire harness or hose could cause a short circuit, engine stall, or fire.

    Product
    ISUZU — ISUZU, CHEVROLET NPR HD, LOW CAB FORWARD 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V720000·2020-11-20

    Isuzu and Chevrolet Trucks Recalled for Battery Cable Fire Risk

    Isuzu and Chevrolet are recalling 2020 NPR-HD and 4500 trucks because a battery cable may overheat near the exhaust, posing a fire risk.

    Product
    ISUZU — ISUZU, CHEVROLET NPR HD, LOW CAB FORWARD 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide