The Recall Desk

State

Arizona product recalls

73,104 recalls have nationwide distribution and so reach Arizona. 8,385 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total
8,385
Critical
1,313
Severe
1,719
Most recent
2026-09-23

Of the 8,385 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 1,719 (21%) are Severe.

These figures cover only the 8,385 recalls whose distribution notice names Arizona specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11601–11625 of 81489

  • HighCPSC·24278·2024-06-20

    Orly Lavender Scented Candles Recalled for Fire and Burn Hazards

    CBOCS Distribution Inc. is recalling about 3,600 lavender scented candles in wooden bread bowls sold at Cracker Barrel Old Country Store from November 2023 through May 2024. The candle flames can reach excessive heights and ignite the wooden bowl, posing fire and burn risks.

    Product
    Lavender scented candles in a round wooden bread bowl
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V466000·2024-06-20

    Fisker Ocean exterior door handles can stick and fail to open

    Fisker is recalling all 2023-2024 Ocean vehicles because the exterior door handles can stick and fail to open, which can prevent occupants from exiting in an emergency.

    Product
    FISKER — FISKER OCEAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24277·2024-06-20

    Head Rush Technologies Recalls TRUBLUE iQ Auto Belay Devices for Fall Hazard

    Head Rush Technologies is recalling TRUBLUE iQ Auto Belay Devices because they can fail to retract, creating a risk of serious injury or death from falls. About 2,200 units were sold online from November 2022 through February 2024.

    Product
    TRUBLUE iQ Auto Belay Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24269·2024-06-20

    StyleCraft Instinct Cordless Hair Clippers Recalled for Fire and Burn Hazards

    StyleCraft is recalling about 50,000 Instinct Professional Vector Motor Cordless Hair Clippers because the lithium-ion battery can overheat, posing fire and burn hazards. Six incidents of battery overheating or fire have been reported, including one minor burn.

    Product
    Instinct Professional Vector Motor Cordless Hair Clippers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24275·2024-06-20

    Babboe Cargo Bicycles Recalled for Frame Cracking and Fall Hazard

    Babboe cargo bicycles manufactured by Babboe B.V. are being recalled because their frames can crack, bend, and break, posing a fall hazard to riders. The recall affects about 300 units sold in the United States through bicycle retailers nationwide between January 2011 and March 2024.

    Product
    Cargo bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24279·2024-06-20

    Cedona Natural View Six-Drawer Dressers Recalled for Tip-Over Hazard

    Global Homes USA is recalling about 400 Cedona Natural View six-drawer dressers sold at Rooms To Go for tip-over and entrapment hazards that can injure or kill children if not anchored to a wall.

    Product
    Cedona Natural View six-drawer dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V461000·2024-06-20

    Toyota Grand Highlander curtain airbags may deploy outside an open window

    Toyota is recalling certain 2024 Grand Highlander and Lexus TX vehicles because the side curtain airbags may not unroll as intended and could partially deploy outside an open window.

    Product
    TOYOTA — TOYOTA, LEXUS GRAND HIGHLANDER, TX, GRAND HIGHLANDER HYBRID, TX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V459000·2024-06-20

    Cadillac XT5 and XT6 instrument panels may not illuminate signal reminders

    GM is recalling certain 2023-2025 Cadillac XT5 and XT6 vehicles because the instrument panel may not illuminate when hazard warning lights, high beams or turn signals are activated.

    Product
    CADILLAC — CADILLAC XT5, XT6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·24V458000·2024-06-20

    Rivian R1S and R1T tire placards show incorrect maximum capacity weight

    Rivian is recalling certain 2022-2023 R1S and R1T vehicles because the maximum vehicle capacity weight value on the tire placard label is incorrect, failing FMVSS 110.

    Product
    RIVIAN — RIVIAN R1T, R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1345-2024·2024-06-19

    Baraka Brand Ground Black Pepper Recalled for Potential Salmonella Contamination

    U.B.C. Food Distributors is recalling Baraka brand ground black pepper due to potential Salmonella contamination. The product is packaged in 7oz retail containers with UPC 8 22514 26626 6.

    Product
    Baraka brand ground black pepper packaged in 7oz retail containers with UPC 8 22514 26626 6; 10 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1353-2024·2024-06-19

    Frozen Scallop Ingredient Recalled Due to Potential Salmonella Contamination

    Kerry, Inc is recalling Scallop Pot Seas frozen scallop ingredient due to potential Salmonella contamination. The product was distributed to commercial customers in multiple U.S. states and Canada.

    Product
    Scallop Pot Seas 703161, 860 kg. SAP Code: 30589206. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Drugs)·D-0554-2024·2024-06-19

    Docetaxel Injection Recalled Nationwide for Stopper Particulate Matter

    Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper contaminating the drug. The recall affects 2,806 vials distributed nationwide.

    Product
    DOCETAXEL — DOCETAXEL (DOCETAXEL ANHYDROUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1356-2024·2024-06-19

    Salt & Vinegar Seasoning Recalled Due to Potential Salmonella Contamination

    Kerry, Inc has recalled Salt & Vinegar seasoning product due to potential Salmonella contamination. The affected product was distributed in multiple U.S. states and Canada.

    Product
    Salt & Vinegar 620592 Net Weight: 50lb (22.68kg) SAP Code: 20644388. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-1921-2024·2024-06-19

    Thoratec HeartMate System Monitor display malfunction in left ventricular assist devices

    The Thoratec HeartMate System Monitor is being recalled due to display malfunctions affecting 4,842 devices worldwide. These issues may prevent proper monitoring and device control.

    Product
    Thoratec HeartMate System Monitor, REF: 1286, L1286, 1286A, L1286A, 1286A-US, L1286A-US, 1286C, L1286C, L1386, 1286A-CAN, 1286INT and L1286INT. Left ventricular assist device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1347-2024·2024-06-19

    Mt. Capra Goat Milk Formula Kit Recalled for Lack of FDA Premarket Notification

    Mt. Capra Goat Milk Formula Recipe Kit recalled for marketing as infant formula without FDA premarket notification.

    Product
    Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. 8oz.) and Bundle Refill. Each Goat Milk Formula Recipe Kit consist of 10 individually packaged ingredients: *Whole Goat Milk *Goat Milk Lactose *Goat Milk Ghee -Extra Virgin Olive Oil -Expeller-Pressed Grapeseed Oil…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1354-2024·2024-06-19

    Seasoning Ingredient Recalled for Potential Salmonella Contamination

    Kerry, Inc is recalling BrS8 RODIZIO Seas No MSG seasoning ingredient due to potential Salmonella contamination. The affected product was distributed to multiple U.S. states and Canada.

    Product
    BrS8 RODIZIO Seas No MSG 9.6#, SAP Code: 20644205. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1355-2024·2024-06-19

    Food ingredient recalled due to potential Salmonella contamination in Sun Nat product

    Kerry Ingredients is recalling 13,341 bags of Sun Nat HV CHDR #3 SEAS food ingredient due to potential Salmonella contamination. No illnesses have been reported.

    Product
    Sun Nat HV CHDR #3 SEAS, Net Weight: 50.00 lb (22.68kg) SAP Code: 20737199. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1357-2024·2024-06-19

    Kerry Cheddar and Sour Cream Seasoning Recall for Potential Salmonella

    Kerry Inc. is recalling 77 bags of Cheddar & Sour Cream SEAS seasoning (lots 8092105, 8127605, 8091886) distributed across multiple U.S. states and Canada due to potential Salmonella contamination.

    Product
    Cheddar & Sour Cream SEAS 22.68kg. Net Weight: 50.00 lb (22.68 kg) SAP Code: 20651520. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0553-2024·2024-06-19

    Docetaxel Injection Recalled Due to Particulate Matter in Stopper

    Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper. Lot F1040001 was distributed nationwide.

    Product
    DOCETAXEL — DOCETAXEL (DOCETAXEL ANHYDROUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2139-2024·2024-06-19

    Aeos Robotic Digital Microscope recalled for safety mechanism failure

    Aesculap Inc is recalling Aeos Robotic Digital Microscope models with Product Code PV010 due to failure of the integrated safety mechanism. The robotic arm may drop more than 10 cm from its original position after the emergency stop button is pressed.

    Product
    Aeos Robotic Digital Microscope, Product Code: PV010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2129-2024·2024-06-19

    OMTech Desktop Laser Engraver recalled for missing safety interlocks

    Rygel Advanced Machines recalls OMTech Desktop Laser Engravers due to missing safety interlocks and labeling. The devices lack required redundant interlocks and certification labels that prevent accidental laser exposure.

    Product
    OMTech Desktop Laser Engraver
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V455000·2024-06-19

    2020–2025 Porsche Taycan front brake hoses can crack

    Porsche is recalling certain 2020–2025 Taycan vehicles because the front brake hoses can develop cracks and leak brake fluid, reducing braking performance. Dealers will replace the hoses for free.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2038-2024·2024-06-19

    EsoFLIP 30mm Balloon Dilation Catheter Recalled for Measurement Inaccuracy

    Covidien is recalling EsoFLIP 30mm balloon dilation catheters due to saline conductivity issues that may cause inaccurate esophageal measurements, potentially leading to patient harm.

    Product
    EsoFLIP, 30mm BALLOON DILATION CATHETER, REF ES-330, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2138-2024·2024-06-19

    EVD Catheter Sterile Packaging Defect Recall for Intracranial Drainage

    Integra LifeSciences is recalling CODMAN BACTISEAL EVD catheters due to external packaging seal defects that may compromise sterility. The recall affects 59 units distributed internationally.

    Product
    CODMAN BACTISEAL Clear EVD Catheter 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0545-2024·2024-06-19

    Prescription Drug Recall: Phenazopyridine Tablets Contain Wrong Medication

    Winder Laboratories is recalling Phenazopyridine HCl tablets (Lot #1142404) due to a product mix-up where some bottles contain Phenobarbital tablets instead. No illnesses or injuries have been reported.

    Product
    PHENAZOPYRIDINE HYDROCHLORIDE — PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide