The Recall Desk

State

Arizona product recalls

73,566 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
1,313
Severe
2,047
Most recent
2026-10-21

Of the 8,391 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.

Which agencies issued them

These figures cover only the 8,391 recalls whose distribution notice names Arizona specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27201–27225 of 81957

  • ModerateFDA (Devices)·Z-1659-2021·2021-05-26

    Bard Groshong NXT ClearVue Catheter Recalled for Connector Defects

    Bard Access Systems is recalling specific Groshong NXT ClearVue catheters due to defects in the distal connector that may prevent proper catheter passage or locking.

    Product
    REF 9617405, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741035989 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1593-2021·2021-05-26

    Gore Viabil Biliary Endoprosthesis Recalled for Length Discrepancy

    W.L. Gore & Associates is recalling 61 Gore Viabil Biliary Endoprosthesis devices because a complaint reported a device appeared shorter than its labeled length.

    Product
    GORE VIBIL Biliary Endoprosthesis: stents, drains and dilators for the biliary ducts. Catalogue numbers: VH1008040, VH1010040, VN1010040, VN0808200 - Product Usage: intended for palliation of malignant strictures in the biliary tree.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0391-2021·2021-05-26

    Sun Pharma Recalls CEQUA Eye Drops for Subpotency and Particulates

    Sun Pharmaceutical Industries is recalling CEQUA (cyclosporine) ophthalmic solution due to subpotent drug levels and the presence of particulates.

    Product
    CEQUA — CEQUA (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0550-2021·2021-05-26

    Faribault Foods Recalls O Organics Organic Chili Beans Due to Seal Defect

    Faribault Foods is recalling O Organics Organic Chili Beans because the cans have compromised hermetic seals. Consumers should stop using the product.

    Product
    O Organics Organic Chili Beans, 15 oz. can, UPC 0-79893- 40617-6 Distributed by Lucerne Foods, Inc. P.O. Box 99, Pleasanton, CA 94566-0009, 1-800-232-4271
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0543-2021·2021-05-26

    21st Century Vitamin D3 Tablets Recalled for Incorrect Labeling

    Twenty-First Century Healthcare is recalling 21st Century Vitamin D3 tablets because some bottles were mislabeled with a lower dosage.

    Product
    21st Century Vitamin D3 125 mcg (5000 IU) tablet, 100 count, UPC 7-40985-27431-6, 21st Century HealthCare, Inc., 2119 Wilson St., Tempe, AZ 85282
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1621-2021·2021-05-26

    Boston Scientific Recalls ELUVIA Drug-Eluting Vascular Stent System Due to Packaging Error

    Boston Scientific is recalling 27 units of the ELUVIA Drug-Eluting Vascular Stent System because some 6x40mm stents were incorrectly placed in 6x100mm packaging.

    Product
    ELUVIA Drug-Eluting Vascular Stent System - Product Usage: indicated for improving luminal diameter in the treatment of symptomatic de-novo or restenotic lesions in the native superficial femoral artery (SFA) and/or proximal popliteal artery with reference vessel diameters (RVD)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0512-2021·2021-05-26

    NOW Health Group Recalls Acidophilus Capsules Due to Foreign Material

    NOW Health Group is recalling 10,235 bottles of NOW 4x6 Acidophilus because foreign capsules were found in the product.

    Product
    NOW 4x6 Acidophilus, 60 capsules per retail bottle. Item number 2920. UPC 7 33739 02920 1
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0548-2021·2021-05-26

    Faribault Foods Recalls S&W Organic Black Beans Due to Compromised Seals

    Faribault Foods is recalling S&W Organic Black Beans because some cans have compromised hermetic seals. Consumers should check their cans and return them for a refund.

    Product
    S&W Organic Black Beans, 15 oz. can, Distributed by: Faribault Foods, 3401 Park Ave NW, Faribault, MN 55021.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0553-2021·2021-05-26

    Udi Gluten Free Blueberry Muffins Recalled for Potential Plastic Presence

    Conagra Brands is recalling Udi Gluten Free Blueberry Muffins due to the potential presence of plastic. Consumers should check lot codes and stop eating the product.

    Product
    Udi Gluten Free Blueberry Muffins, 10oz (284g) retail container of 4 muffins, 6 retail units per wholesale case. Retail unit UPC: 00-6-98997-81038-4 (domestic) 00-6-98997-81044-5 (Canada)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0386-2021·2021-05-26

    KVK-Tech Recalls Hydrocodone and Homatropine Tablets for Impurity Failures

    KVK-Tech, Inc. is recalling 17,096 bottles of Hydrocodone Bitartrate and Homatropine Methylibromide tablets due to failed impurities and degradation specifications.

    Product
    HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE — HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE (HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0387-2021·2021-05-26

    Nomax Recalls Subpotent Dry Eye Test Fluorescein Sodium Strips

    Nomax Inc. is voluntarily recalling 78 cartons of Dry Eye Test strips due to subpotent drug content. The FDA classified this as a Class III recall.

    Product
    DRY EYE TEST — DRY EYE TEST (FLUORESCEIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V385000·2021-05-25

    Van Hool Recalls 681 Buses Due to Fuel Rail Leak Risk

    Van Hool is recalling 681 buses because a sealing washer may not seat correctly, allowing the high-pressure fuel rail to leak and increasing fire risk.

    Product
    VAN HOOL — VAN HOOL CX45, CX35, TX45, TDX25
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V384000·2021-05-25

    Life Line Recalls 2019-2020 RAM 5500 Vehicles for Brake Line Defect

    Life Line Emergency Vehicles is recalling 2019-2020 RAM 5500 vehicles because improperly routed rear brake lines may chafe and leak fluid, increasing crash risk.

    Product
    LIFELINE — LIFELINE RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V389000·2021-05-25

    Tesla Recalls Model 3 and Model Y for Seat Belt Fastener Defect

    Tesla is recalling 2018-2020 Model 3 and 2019-2021 Model Y vehicles because front seat belt fasteners may not be properly attached, increasing injury risk.

    Product
    TESLA — TESLA MODEL Y, MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V387000·2021-05-25

    2020 Tesla Model 3 brake caliper bolts may loosen and separate

    Tesla is recalling certain 2020 Model 3 vehicles because brake caliper bolts may loosen, causing the caliper to separate and lose tire pressure, increasing crash risk.

    Product
    TESLA — TESLA MODEL 3, MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V386000·2021-05-25

    Seagrave Fire Apparatus Recalls 2017-2020 Models Due to Fuel Leak Risk

    Seagrave is recalling 2017-2020 Marauder, Attacker, and Capitol vehicles because a sealing washer defect may cause high-pressure fuel leaks, increasing fire risk.

    Product
    SEAGRAVE — SEAGRAVE MARAUDER, ATTACKER, CAPITAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V390000·2021-05-25

    2021 Ford F-Series trucks recalled for improper front wheel hub attachment

    Ford is recalling 17,616 of its 2021 F-Series trucks with dual rear wheels and front wheel hub extenders. The hub extenders may be improperly attached, risking wheel separation and crash.

    Product
    FORD — FORD F-450 SD, F-550 SD, F-350 SD, F-600 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V379000·2021-05-24

    2021 Ford F-350 and F-450 Cracked Fifth Wheel Mounting Bracket Recall

    Ford is recalling certain 2021 F-350 SD and F-450 SD vehicles with fifth wheel left-hand mounting brackets that may be cracked. A cracked bracket could result in the fifth wheel detaching during towing, increasing crash risk.

    Product
    FORD — FORD F-450 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V381000·2021-05-24

    Ford Recalls 2021 F-150 Trucks Due to Driveshaft Assembly Defect

    Ford is recalling 2021 F-150 vehicles because improperly assembled driveshafts may separate, potentially causing loss of drive power or unintended movement.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V383000·2021-05-24

    Great Dane Recalls 2022 Champion Trailers Due to Brake Bolt Issue

    Great Dane is recalling 2022 Champion trailers because brake caliper bolts may loosen, reducing brake effectiveness and increasing crash risk.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V382000·2021-05-24

    Honda Motorcycles Recalled for Defective Rear Reflectors

    Honda is recalling certain 2020-2021 motorcycles because the rear reflector lens may not reflect brightly enough. This defect reduces visibility and increases the risk of crashes or injuries.

    Product
    HONDA — HONDA CBR500R, CB500X, C125, CB650R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V377000·2021-05-24

    2021 Ford Edge vehicles recalled for defective seatbelt retractors

    Ford is recalling certain 2021 Edge vehicles for a defective driver's seatbelt retractor pretensioner assembly that may fail to function during a crash. A faulty seatbelt increases injury risk in accidents.

    Product
    FORD — FORD EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide