The Recall Desk

State

Arizona product recalls

73,495 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.

These figures cover only the 8,390 recalls whose distribution notice names Arizona specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24926–24950 of 81885

  • HighNHTSA·21V875000·2021-11-12

    Mazda Recalls 2018-2020 Models for Fuel Pump Failure Risk

    Mazda is recalling 121,038 vehicles from 2018-2020 because a fuel pump impeller may crack, causing engine stalls and increasing crash risk.

    Product
    MAZDA — MAZDA MAZDA2, CX-9, MX-5, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V877000·2021-11-12

    2021-2022 Forest River Cherokee Travel Trailers Recalled for Incorrect Tire Placard

    Forest River is recalling 2021-2022 Cherokee travel trailers because the tire size and weight rating printed on the Federal Placard are incorrect. This could cause the vehicle to be overloaded and lose control.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22709·2021-11-12

    Hanna Andersson Baby Long Sleeve Wiggle Sets Recalled for Choking Hazard

    Hanna Andersson is recalling about 4,400 Baby Long Sleeve Wiggle Sets because snaps on the long sleeve top can detach, creating a choking hazard for young children. Consumers should stop using the product immediately and contact Hanna Andersson for a full refund.

    Product
    Baby Long Sleeve Wiggle Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22710·2021-11-12

    Hanna Andersson Baby Ruffle Rompers Recalled for Choking Hazard

    Hanna Andersson is recalling about 3,200 Baby Ruffle Rompers because metal snaps on the garment can detach, posing a choking hazard to infants and young children. The company is offering a full refund.

    Product
    Baby Ruffle Rompers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22708·2021-11-12

    VidaXL Steel Pool Ladders Recalled for Fall and Drowning Hazards

    VidaXL is recalling approximately 3,200 steel pool ladders because the steps can loosen during use, creating a risk of falls and drowning. Four fall incidents have been reported with no injuries.

    Product
    VidaXL Steel Pool Ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·042-2021·2021-11-10

    Citterio Salame Sticks Recalled for Possible Salmonella Contamination

    Euro Foods is recalling Citterio salame sticks due to possible Salmonella contamination linked to a multistate outbreak.

    Product
    Euro Food, Inc., DBA Citterio USA Corporation — Euro Foods Dba Citterio USA Corp. Recalls Salame Stick Products Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V873000·2021-11-10

    Jeep Wagoneer and Grand Cherokee Airbag Control Software Defect

    The Occupant Restraint Controller software in certain 2021-2022 Jeep models may be faulty, allowing airbags to disable without warning. This increases crash injury risk.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND WAGONEER, WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0093-2022·2021-11-10

    Cubicin daptomycin injection recalled for glass particle contamination

    Merck Sharp & Dohme Corp. is recalling Cubicin (daptomycin for injection) 500 mg vials due to the presence of glass particles. The recall affects a single lot distributed nationwide.

    Product
    Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial, Rx only. Manuf. for: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, USA. Manuf. by: Baxter Pharmaceuticals LLC., Bloomington, IN 47403, USA, NDC: 67919-011-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0113-2022·2021-11-10

    ProSource Produce white onions recall for Salmonella contamination

    ProSource Produce LLC is recalling whole raw white onions imported from Mexico due to potential Salmonella Oranienburg contamination. The onions were distributed across 33 U.S. states and Canada.

    Product
    Whole raw WHITE onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3 lb., and 2 lb. mesh sacks and in 50 lb., 40 lb., 25 lb., 10 lb., and 5 lb. cartons. Products are distributed and/or sold under the brands Big Bull…
    Category
    Food
    Distribution
    36 states
  • SevereUSDA FSIS·043-2021·2021-11-10

    Innovative Solutions Recalls Chicken Patties Due to Possible Bone Contamination

    Innovative Solutions, Inc. is recalling raw chicken patty products that may contain pieces of bone. No illnesses have been reported.

    Product
    Innovative Solutions, Inc — Innovative Solutions, Inc. Recalls Chicken Patty Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0194-2022·2021-11-10

    IPL Coupling Gel and EcoGel 200 Recalled for Bacterial Contamination

    Lumenis, Inc. is recalling IPL Coupling Gel and EcoGel 200 due to potential bacterial contamination. Approximately 11,064 units were distributed worldwide.

    Product
    IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL Coupling Gel or EcoGel 200, 0.25 L (AX1009012) manufactured by Eco-Med Pharmaceutical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0089-2022·2021-11-10

    Irbesartan and Hydrochlorothiazide Tablets Recalled for Impurity Contamination

    Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets 150/12.5 mg due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient, which resulted from CGMP deviations.

    Product
    Irbesartan and Hydrochlorothiazide Tablets USP, 150/12.5 mg a) 30 count (NDC 68180-413-06) and b) 90 count (NDC 68180-413-09) bottles, Rx only
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0087-2022·2021-11-10

    Irbesartan Tablets Recalled for Impurity in Active Ingredient

    Lupin Pharmaceuticals is recalling Irbesartan tablets due to the detection of N-nitrosoirbesartan impurity in the active pharmaceutical ingredient. The recall affects 30-count and 90-count bottles distributed nationwide.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0111-2022·2021-11-10

    Raw Red Onions Recalled Due to Salmonella Oranienburg Risk

    ProSource Produce LLC has recalled whole raw red onions imported from Chihuahua, Mexico, due to potential Salmonella Oranienburg contamination. The affected product was distributed across multiple U.S. states and Canadian provinces.

    Product
    Whole raw RED onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3 lb., and 2 lb. mesh sacks and in 50 lb., 40 lb., 25 lb., 10 lb., and 5 lb. cartons. Products are distributed and/or sold under the brands Big Bull, Markon…
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Drugs)·D-0092-2022·2021-11-10

    Methocarbamol Tablets Mislabeled with Incorrect Strength

    Bryant Ranch Prepack is recalling Methocarbamol 500mg tablets nationwide because the bottles are mislabeled—they actually contain 750mg tablets. The affected lot was distributed in 30-, 60-, and 90-count bottles.

    Product
    Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0090-2022·2021-11-10

    Lupin Pharmaceuticals Irbesartan/Hydrochlorothiazide Tablets Recalled for Impurity

    Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets USP (300/12.5 mg) in 30-count and 90-count bottles due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient.

    Product
    Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0134-2022·2021-11-10

    Cedar's Organic Mediterranean Hummus recalled for undeclared tree nuts

    Cedar's Organic Mediterranean Hummus 10 oz. is being recalled because it may contain undeclared pine nuts, a tree nut allergen. Consumers with tree nut allergies should not consume this product.

    Product
    Cedar s Organic Mediterranean Hommus 10 oz.
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·F-0112-2022·2021-11-10

    Raw Yellow Onions from Mexico Recalled for Salmonella Oranienburg

    ProSource Produce LLC is recalling whole raw yellow onions imported from Chihuahua, Mexico, due to potential contamination with Salmonella Oranienburg. The affected onions were distributed across multiple U.S. states and Canadian provinces under various brand names.

    Product
    Whole raw YELLOW onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3 lb., and 2 lb. mesh sacks and in 50 lb., 40 lb., 25 lb., 10 lb., and 5 lb. cartons. Products are distributed and/or sold under the brands Big Bull…
    Category
    Food
    Distribution
    36 states
  • SevereNHTSA·21V872000·2021-11-10

    Maserati Vehicles Recall: Fuel Line Sensor Housing May Crack and Leak

    Maserati is recalling certain 2021-2022 model-year vehicles due to a defective fuel line sensor housing that may crack and leak fuel. The leak can cause engine stall or fire, increasing crash risk.

    Product
    MASERATI — MASERATI GHIBLI, QUATTROPORTE, LEVANTE, MC20
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V871000·2021-11-10

    Ram 1500 Recalled for Inoperable Windshield Defrosting System

    Chrysler is recalling 2022 Ram 1500 vehicles because incompatible HVAC systems may render the windshield defrosting and defogging system inoperable, reducing driver visibility.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0191-2022·2021-11-10

    Lisendo 880 Ultrasound Software displays incorrect cardiac valve measurements

    Lisendo 880 Ultrasound Software versions V1.0–V4.1.3 may not display cardiac measurement results correctly for mitral valve assessments, affecting diagnostic accuracy.

    Product
    Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0195-2022·2021-11-10

    Siemens COVID-19 Diagnostic Assay Recalled for Inadequate Validation Data

    Siemens is recalling Atellica IM SARS-CoV-2 Antigen Assay kits because validation data submitted to the FDA was insufficient to confirm the assay's accuracy for its intended use.

    Product
    Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit), SMN # 11207861
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0186-2022·2021-11-10

    Flexor Check-Flo Introducer Sets recalled due to misplaced radiopaque marker band

    Cook Inc. recalls Flexor Check-Flo Introducer Sets where the radiopaque marker band is incorrectly positioned, which may not be discovered until the device is used in a patient under fluoroscopy, increasing procedural time.

    Product
    Flexor Check-Flo Introducer - Raabe Modification, Introducer Set, RPN KCFW-5.0-38-90-RB-RAABE, GPN G13069 The introducer sheath incorporates a hydrophilic coated Flexor shaft with a hemostasis valve and is provided with a dilator.
    Category
    Medical Device
    Distribution
    17 states
  • HighNHTSA·21V874000·2021-11-10

    Audi Recalls A4, A5, S4, S5, RS 5 Models Due to Air Bag Defect

    Audi is recalling specific 2017-2020 models because a cable fault may disable the passenger air bag, increasing injury risk in a crash.

    Product
    AUDI — AUDI A4, A5, RS 5, S5
    Category
    Vehicle
    Distribution
    Distributed nationwide