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.

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.

29176–29200 of 81987

  • HighFDA (Devices)·Z-0452-2021·2020-11-25

    Cardinal Health Recalls Kangaroo Connect 500ml Bag Sets Due to Leakage

    Cardinal Health is recalling Kangaroo Connect 500ml Bag Sets because they may leak at the tube and spike connector interface.

    Product
    Kangaroo Connect 500ml Bag Set, Non-Sterile, Product Code 77500FD - Product Usage: single-use tubing sets used with pumps in the delivery of nutritional feeding product.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0457-2021·2020-11-25

    Stryker Recalls Osteosynthesis Compression Staple EasyClip Devices

    Stryker GmbH is recalling EasyClip and EasyClip Xpress staples due to potential nickel release above safety margins in pediatric patients under 20 kg.

    Product
    Osteosynthesis Compression Staple EasyClip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V737000·2020-11-25

    Audi recalls S5, A5, and RS5 for rear wiring defect

    Volkswagen Group (Audi) is recalling 2020-2021 S5, A5, and RS5 vehicles due to missing anti-abrasion protection on rear light wiring. In a crash, exposed wires may be damaged, potentially disabling door locks and hazard lights.

    Product
    AUDI — AUDI S5, A5, RS 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0116-2021·2020-11-25

    Art Of Tea Feel Better tea recalled for potential Salmonella

    Art Of Tea is recalling Feel Better tea due to potential Salmonella contamination in elder berries. Consumers should stop using the product.

    Product
    Art Of Tea - Feel Better tea; Produced and Distributed by: Art of Tea LLC, Monterey Park, CA Directions: 1 Tbsp of tea in 8 oz. of water at 206 degrees; steep for 5-7 minutes. Packaged in: Black Mylar bag with label, Silver Mylar bag with label, Silver Tin Canisters…
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-0454-2021·2020-11-25

    MeritMedical Cultura Flex Swab Recall Due to Tip Breakage Risk

    Merit Medical Systems is recalling Cultura Flex Swabs because the flocked tip may break off during use, potentially causing soft tissue injury or treatment delays.

    Product
    MeritMedical Cultura Flex Swab, Sterile Flocked Collection Device, Ref C100F, Sterile, for the following unit count:1 unit - (01)00884450491102, 25 unit - (01)10884450491109, 100 unit - (01)20884450491106
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0449-2021·2020-11-25

    Thomas Scientific Recalls Wuxi Nest Patient Specimen Collection Tubes

    Thomas Scientific is recalling Wuxi Nest patient specimen collection tubes to replace units manufactured and distributed prior to Enforcement Discretion Approval.

    Product
    Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21036·2020-11-25

    Santa Cruz Recalls 2020 Aluminum Bicycles Due to Frame Buckling Risk

    Santa Cruz Bicycles is recalling about 2,900 model year 2020 aluminum frames because thermal damage can cause them to bend or buckle, posing a fall hazard.

    Product
    Model Year 2020 Aluminum Santa Cruz and Juliana Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21034·2020-11-25

    RH Recalls Wine Barrel Chandeliers Due to Falling Hardware Hazard

    RH is recalling approximately 7,800 wine barrel chandeliers because hanging hardware can break, causing the fixture to fall. No injuries have been reported.

    Product
    Wine Barrel Chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V734000·2020-11-25

    Toyota RAV4 and Avalon Steering Column Airbag Failure Recall

    Certain 2020-2021 Toyota RAV4, RAV4 Hybrid, Avalon, and Avalon Hybrid vehicles may have damaged steering column breakaway pins that could reduce airbag performance in a crash. Toyota will replace the steering column at no cost.

    Product
    TOYOTA — TOYOTA RAV4 HYBRID, AVALON HYBRID, AVALON, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V733000·2020-11-25

    Renegade Motorhomes Recalled for Gas Leak Risk in Cooking Stove

    Kibbi is recalling certain 2019-2021 Renegade motorhomes with Dometic cooking stoves due to a potential gas leak from an overtightened saddle valve bolt, which could increase fire risk. Dealers will install repair kits free of charge.

    Product
    RENEGADE — RENEGADE VERONA LE, VERONA, VALENCIA, CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0472-2021·2020-11-25

    Mako MICS Handpiece Recalled for Potential Bone Preparation Discrepancies

    Stryker is recalling Mako MICS Handpieces due to a characterization issue that may cause unsuccessful checkpoint verification or bone cuts differing from the preoperative plan.

    Product
    Mako Integrated Cutting System (MICS) Handpiece, Catalog Number 209063, Software Version#: THA 3.0 and later, PKA 3.0 and later, and TKA 1.0 - Product Usage: The MICS Handpiece is attached to the distal end of the robotic arm and is used to register the RIO (Mako robot) and to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0453-2021·2020-11-25

    Cardinal Health Recalls Kangaroo Connect 1000ml Bag Sets Due to Leak Risk

    Cardinal Health 200, LLC is recalling Kangaroo Connect 1000ml Bag Sets because the feeding spike sets may leak at the tube and spike connector interface.

    Product
    Kangaroo Connect 1000ml Bag Set, Non-Sterile, Product Code 77100FD - Product Usage: single-use tubing sets used with pumps in the delivery of nutritional feeding product.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0455-2021·2020-11-25

    Merit Medical Cultura Collection and Transport System recall due to swab tip breakage risk

    Merit Medical recalls its Cultura Collection and Transport System because the swab tip may break off during sample collection, potentially causing soft tissue injury.

    Product
    Merit Medical Cultura Collection and Transport System, Ref CFTS100, Single Use, IVD, for the following unit counts: 1 Unit - (01)00884450492123, 50 Units - (01)10884450492120, 200 units - (01)20884450492127
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0461-2021·2020-11-25

    Roche Recalls cobas infinity Software Due to Incorrect Validation

    Roche Diagnostics is recalling 40 cobas infinity central lab licenses because an erroneous QC status may cause incorrect validation of results.

    Product
    cobas infinity central lab/cobas infinity core license-The cobas infinity IT solutions application is intended to be used for the configuration and connectivity management of instruments and software systems Catalog Number: 07154003001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V736000·2020-11-25

    GM Recalls 2015-2016 Silverado and Sierra Trucks for Air Bag Defect

    General Motors is recalling 2015-2016 Chevrolet Silverado and GMC Sierra trucks because the roof-rail air bag inflator end cap may detach, posing an injury risk.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500, SIERRA 2500, SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0456-2021·2020-11-25

    Merit Medical Cultura Collection and Transport System Swab Tip Breakage Recall

    Merit Medical is recalling Cultura Collection and Transport Systems because the swab tip may break off during sample collection, potentially causing soft tissue injury.

    Product
    Merit Medical Cultura Collection and Transport System, 3 mL Viral Transport Medium, Ref: VCTS100, Single Use, IVD, for the following unit counts: 1 Unit - (01)00884450499917, 50 Units - (01)10884450499914, 200 units - (01)20884450499911
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21033·2020-11-25

    Herobility Eco Baby Spoons and Feeding Sets Recalled for Choking Hazard

    Herobility is recalling Eco Baby Spoons, Forks, and Feeding Sets because they can break into small pieces, posing a choking hazard. No injuries have been reported.

    Product
    Baby Spoons and Forks, Feeding Spoons and Placemat Feeding sets 4PCs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V735000·2020-11-25

    Front Seat Bolts May Not Be Installed Properly in 2021 Chevrolet Tahoe

    Front seat attachment bolts may not have been properly installed on certain 2021 Chevrolet Tahoe, Suburban, and GMC Yukon models. If loose or missing, the seats could move during a crash, increasing injury risk.

    Product
    GMC — GMC, CHEVROLET YUKON, YUKON XL, TAHOE, SUBURBAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0473-2021·2020-11-25

    Siemens Atellica IM 1300 Analyzer Recalled for Test Definition Scanning Issues

    Siemens Healthcare Diagnostics is recalling Atellica IM 1300 Analyzers because scanning specific test definitions may reset custom settings, causing inaccurate test results.

    Product
    Atellica IM 1300 Analyzer - Product Usage: automated, immunoassay analyzers designed to perform in vitro diagnostic tests on clinical specimens. Siemens Material Number (SMN): 11066001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0451-2021·2020-11-25

    Ortho Recalls VITROS Anti-SARS-CoV-2 IgG Control Due to Signal Issues

    Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 IgG Control and Calibrator lots due to elevated signal/cutoff values and decreased signal.

    Product
    VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product Usage: For use in monitoring the performance of the VITROS Immunodiagnostic and Integrated Systems when used for the determination of IgG antibodies to SARS-CoV-2. Product Code (Unique Identifier)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0462-2021·2020-11-25

    LivaNova VNS Therapy AspireSR Generator Recall for Serial Number Error

    LivaNova is recalling 134 VNS Therapy AspireSR Generators because an extra digit in the serial number makes them incompatible with specific therapy programmers.

    Product
    VNS Therapy¿ AspireSR¿ Generator
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Drugs)·D-0106-2021·2020-11-25

    Apotex Recalls Aripiprazole Tablets Due to Dissolution Failures

    Apotex Corp. is recalling Aripiprazole Tablets 15 mg because they failed to meet dissolution specifications. The affected products were distributed nationwide in the USA.

    Product
    Aripiprazole Tablets, USP 15 mg tablets, packaged in a) 1000 count bottle, NDC 60505-2675-8; b) 30 count bottle, NDC 60505-2675-3; Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326
    Category
    Drug
    Distribution
    Distributed nationwide