The Recall Desk

State

Arizona product recalls

73,388 recalls have nationwide distribution and so reach Arizona. 8,387 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total
8,387
Critical
1,313
Severe
2,047
Most recent
2026-10-02

Of the 8,387 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 8,387 recalls whose distribution notice names Arizona specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21676–21700 of 81775

  • HighFDA (Drugs)·D-1151-2022·2022-06-29

    Isopropyl Alcohol bottles recalled for defective containers and leakage

    Vi-Jon's 70% isopropyl alcohol bottles may leak when squeezed or tilted due to defects in the bottle neck finish. Over 3 million bottles with various lot numbers were distributed nationwide.

    Product
    ISOPROPYL ALCOHOL — ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1155-2022·2022-06-29

    Clonazepam Tablets Recalled Due to Manufacturing Defect

    Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets (0.125mg) due to manufacturing defects where oversized tablets were found. The affected lot (MHC1430A, exp. 09/2023) was distributed nationwide.

    Product
    Clonazepam Orally Disintegrating Tablets, USP, 0.125mg, Rx Only, 60 Tablets, Mfd. by: Sun Pharmaceutical Industries Ltd. Mumbai, India, Dist. by: Sun Pharmaceutical Industries In., Cranbury, NJ 08512, NDC 57664-783-68, packaged in bottles.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1280-2022·2022-06-29

    FDA Recalls Metalogix Slotted 90 Tubular Wrench Due to Manufacturing Error

    New Standard Device Inc is recalling 14 Metalogix Slotted 90 Tubular Wrenches (Lot A29618A) due to a manufacturing error that causes the wrench to strip nuts when torqueing. No injuries have been reported.

    Product
    Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1281-2022·2022-06-29

    BVI Wet-Field Eraser surgical devices shipped with incorrect tip configuration

    Beaver Visitec International recalled 660 units of BVI Wet-Field Eraser surgical devices after discovering boxes labeled with one tip configuration contained a different tip design. This mismatch could affect surgical precision and hemostasis control.

    Product
    BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high frequency electrical current Part Number: 221251
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1342-2022·2022-06-29

    Mia's Bakery Banh Xu Dua Cake Recalled for Undeclared Coconut

    Mia's Bakery recalls Banh Xu Dua cake because coconut is not declared on the product label, posing a risk to consumers with coconut allergies.

    Product
    Mia's Bakery Bahn Xu Dua Wt. 7 oz./198.5 gram UPC: 8 50660 00003 8 Ings: Glutinous Rice Flour, Sugar, Mung Bean, Soy Bean Oil, Water, Sesame Oil, Sodium Benzoate, Black Color, FD & C Yellow 5 & 6, Red #4 and Blue #1. Keep refrigerated after opening 1965 Potrero Grande…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1282-2022·2022-06-29

    INTERGARD Woven Vascular Graft mislabeled with incorrect size specification

    Maquet Cardiovascular recalls INTERGARD Woven Vascular Grafts with incorrect labeling. Units labeled as 8 mm diameter instead contained 32 mm diameter grafts.

    Product
    INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2022·2022-06-29

    Cardiac device software recalled for inadequate electrical insulation

    CardioTek EP-TRACER Software V2.x is recalled because it failed electrical safety testing for insulation. The 146 affected units were distributed worldwide.

    Product
    CardioTek EP-TRACER Software V2.x.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1275-2022·2022-06-29

    EVIS EXERA II Gastrointestinal Videoscope Recalled for Incorrect Component Fit

    Olympus is recalling 8 EVIS EXERA II gastrointestinal videoscopes (Model GIF-HQ190) because an incorrect rubber component may have been installed during repair. The incorrect part does not meet the device's design specifications.

    Product
    EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model: GIF-HQ190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1346-2022·2022-06-29

    Wise Woman Herbals Kava Capsules recalled for yeast and mold contamination

    EarthLab Inc is recalling Wise Woman Herbals Kava Capsules nationwide due to microbial contamination. Quality testing found yeast and mold counts that exceeded acceptable levels.

    Product
    Wise Woman Herbals Kava Capsules, 450 mg Kava (Piper met. Root), Dosage: 1 capsule up to 3 times per day day at 450mg Kava root. 90 counts per bottle. UPC 7 48840 14284 8. Kava Capsules older lots are packaged in 250cc Wide Mouth Amber Glass Packer, Black 45/400 PP ribbed…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1348-2022·2022-06-29

    Wise Woman Herbals Sleepytime Glycerite Recalled for Yeast and Mold Contamination

    EarthLab Inc is recalling Wise Woman Herbals Sleepytime Glycerite due to elevated yeast and mold levels detected in microbial testing. Consumers should discontinue use.

    Product
    Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength is 20% presence in formula. Dosage: 60 drops 1-4 times a day. Product is packaged in Amber Glass Boston Round bottle, Black serrated polypropylene dropper assembly with rubber bulb (2oz only) or Black…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1343-2022·2022-06-29

    Pedialyte with Immune Support Recalled for Potential Container Leakage

    Abbott Laboratories is recalling specific lots of Pedialyte with Immune Support in 1L containers due to potential leakage. Approximately 50,502 2-count cases are affected across 28 states.

    Product
    Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural & Artificial Flavor, 33.8 FL OZ (1.05 QT) 1L***INGREDIENTS: WATER, DEXTROSE*** Abbott Nutrition, Abbott Laboratories, Columbus, Ohio 43219-3034 USA
    Category
    Food
    Distribution
    28 states
  • ModerateFDA (Drugs)·D-1152-2022·2022-06-29

    FDA Recalls Clonidine Transdermal Patches for Delivery System Defect

    Mayne Pharma is recalling 1,440 cartons of Clonidine transdermal patches nationwide due to an out-of-specification defect in the release liner that could affect proper drug delivery.

    Product
    CLONIDINE — CLONIDINE (CLONIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1344-2022·2022-06-29

    Pedialyte Immune Support Raspberry Lemonade recalled for container leakage risk

    Abbott Laboratories is recalling approximately 121,918 cases of Pedialyte with Immune Support Raspberry Lemonade due to potential container leakage. The recall affects multiple states.

    Product
    Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Raspberry Lemonade Natural & Artificial Flavor, 33.8 FL OZ (1.05 QT) 1L*** INGREDIENTS: WATER, DEXTROSE***Abbott Nutrition, Abbott Laboratories, Columbus, Ohio 43219-3034 USA
    Category
    Food
    Distribution
    28 states
  • CriticalUSDA FSIS·020-2022·2022-06-28

    Creminelli Recalls Mini Parmesan Salami Sticks Due to Undeclared Egg Allergen

    Creminelli Fine Meats is recalling approximately 4,207 pounds of mini parmesan salami sticks because the product contains an undeclared egg allergen.

    Product
    Creminelli Operating LLC — Creminelli Fine Meats Recalls Mini Parmesan Salami Stick Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V459000·2022-06-28

    Hyundai Recalls 2017-2018 Ioniq Hybrids for Fire Risk

    Hyundai is recalling 2017-2018 Ioniq Hybrid and Plug-in Hybrid vehicles because a power relay assembly may overheat, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI IONIQ HYBRID, IONIQ PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V458000·2022-06-27

    2020-2022 Hyundai Venue seat belt pretensioners may explode in crash

    Hyundai is recalling 2020-2022 Venue vehicles because the front seat belt pretensioners may explode when deployed in a crash, potentially projecting metal fragments at occupants.

    Product
    HYUNDAI — HYUNDAI VENUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V452000·2022-06-24

    Airstream Recalls 2022 Travel Trailers Due to Hub Assembly Defect

    Airstream is recalling 2022 Caravel, Flying Cloud, Globetrotter, International, and Pottery Barn travel trailers because a bearing washer may crack, causing the hub to separate from the axle.

    Product
    AIRSTREAM — AIRSTREAM POTTERY BARN, CARAVEL, INTERNATIONAL, GLOBETROTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V455000·2022-06-24

    2022 Lincoln Navigator Headlight Control Software Defect Causes Light Failure

    Ford is recalling certain 2022 Lincoln Navigator vehicles due to headlight control module software that may fail, causing side marker and daytime running lights to go dark. This increases crash risk from reduced visibility.

    Product
    LINCOLN — LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V451000·2022-06-24

    2022 Ford Bronco Windshield May Separate During Crash

    Certain 2022 Ford Broncos and Rangers have windshields that may not be properly bonded and could separate during a crash, increasing injury risk.

    Product
    FORD — FORD RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V457000·2022-06-24

    2021 Nissan Frontier transmission parking pawl failure may cause vehicle rollaway

    Certain 2020-2022 Nissan Frontier and Titan vehicles have a defective transmission parking pawl that may not engage when shifted to park, creating a rollaway risk. Dealers will replace the component at no cost.

    Product
    NISSAN — NISSAN TITAN, FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V454000·2022-06-24

    2022 Lincoln Aviator Engine Rails Defect Increases Crash Injury Risk

    Ford is recalling certain 2022 Lincoln Aviator vehicles due to improperly heat-treated engine rails that may reduce structural protection in crashes and potentially detach while driving. Owners should contact Ford for a free inspection and replacement.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide