The Recall Desk

State

Arkansas product recalls

20,096 recalls have nationwide distribution and so reach Arkansas. 0 additional recalls listed Arkansas specifically in their distribution scope.

About recalls in Arkansas

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Arkansas consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

8151–8175 of 20096

  • HighFDA (Food)·F-1572-2024·2024-08-07

    Amafruit Superfruits Recalled for Possible Listeria Contamination Nationwide

    Totally Cool, Inc. is recalling Amafruit Superfruits from the Amazon Dragon Fruit due to possible Listeria monocytogenes contamination. The product has been distributed nationwide; consumers should discard or return affected lots.

    Product
    Amafruit Superfruits from the Amazon Dragon Fruit. Packaged in 3 gallon plastic tubs, UPC 855738002242.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1546-2024·2024-08-07

    Friendly's Strawberry Krunch Ice Cream Cake recalled for possible Listeria contamination

    Friendly's Strawberry Krunch Ice Cream Cake is being recalled due to possible Listeria monocytogenes contamination. Approximately 86,540 cases distributed nationwide are affected.

    Product
    Friendly's Strawberry Krunch Ice Cream Cake 40 fl oz, UPC 29839413065. Packaged in cardboard box, 4 boxes per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2452-2024·2024-08-07

    Boston Scientific Capio SLIM Device May Fail During Surgical Procedures

    Some lots of the Capio SLIM suture capturing device may fail to consistently catch sutures during surgery, potentially requiring extended procedures or additional medical intervention.

    Product
    Capio SLIM Suture Capturing Device, 1-Pack, UPN: M0068318250. Capio SLIM Suture Capturing Devices are used by physicians to facilitate the consistent placement of sutures during open surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1738-2024·2024-08-07

    Urban Outfitters Elin Dessert Plates Recalled for Elevated Cadmium Levels

    Urban Outfitters is recalling Elin Dessert Plates due to elevated cadmium levels. The lilac plates with mushroom and fern motifs were distributed nationwide.

    Product
    Elin Dessert Plates. The recalled plates are lilac in color with orange mushroom, moth, and fern motifs. The plates measure 21 cm (8.25 inches) in diameter and have scalloped edges. Plates sold individually in store.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1554-2024·2024-08-07

    Yelloh! Ice Cream Sandwiches Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Yelloh! Chocolate Chip Ice Cream Sandwiches nationwide for possible Listeria monocytogenes contamination. Do not consume; dispose of or return the product (codes 6T3115–6T4171).

    Product
    Yelloh! Chocolate Chip Ice Cream Sandwich With Vanilla Ice Cream 24 fl oz UPC 810038685106. Individually wrapped in plastic. 6 sandwiches packaged in cardboard box, 12 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2455-2024·2024-08-07

    Clinical Chemistry Analyzer Software Bugs May Cause Erroneous Patient Results

    Beckman Coulter's DxC 500 AU analyzer has two software bugs that may cause erroneous patient results due to misreported calibrations or expired reagents. No injuries or illnesses have been reported.

    Product
    DxC 500 AU Clinical Chemistry Analyzer, REF C63520 is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate reagents, calibrators, quality control (QC) material and other accessories. This system is for in vitro diagnostic use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1551-2024·2024-08-07

    Hershey's ice cream sheet cake recalled for possible Listeria contamination

    Totally Cool, Inc. is recalling Hershey's ice cream sheet cake due to possible contamination with Listeria monocytogenes. The FDA Class II recall affects 14,180 cases distributed nationwide.

    Product
    Hershey s Ice Cream Vanilla & Chocolate Flavored Ice Cream Sheet Cake 110 fl oz, UPC 24682060152. Packaged in cardboard box, 3 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1574-2024·2024-08-07

    Frozen Farms Raspberry Sorbet Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling The Frozen Farms Farm Crafted Raspberry Sorbet due to possible Listeria monocytogenes contamination. The affected product was distributed nationwide.

    Product
    The Frozen Farms Farm Crafted Rasberry Sorbet 16 fl oz/1 pint, UPC 850023398116. Packaged in paper containers, 8 containers per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1594-2024·2024-08-07

    Marco Turkish Mocha Ice Cream Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Marco Turkish Mocha Ice Cream 16 fl oz due to possible Listeria monocytogenes contamination. Consumers should not consume affected products.

    Product
    Marco Turkish Mocha Ice Cream 16 fl oz/1 pint, UPC 860001992885. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1584-2024·2024-08-07

    LaSalle Cherry Vanilla Ice Cream Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling LaSalle Cherry Vanilla Ice Cream for possible Listeria monocytogenes contamination. The affected product was distributed nationwide.

    Product
    LaSalle Cherry Vanilla Ice Cream 16 fl oz/1 pint, UPC 671891374107. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1565-2024·2024-08-07

    Yelloh! Pecan Praline Sundae Cones recalled for possible Listeria contamination

    Yelloh! Pecan Praline Sundae Cones (4 fl oz) manufactured by Totally Cool, Inc. are being recalled due to possible contamination with Listeria monocytogenes.

    Product
    Yelloh! Pecan Praline Sundae Cones 4 fl oz UPC 810038684925. 12 cones wrapped in paper, packaged in cardboard box, 8 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2454-2024·2024-08-07

    SOFT-VU KUMPE Catheters Recalled for Mislabeled Inner Pouch

    Angiodynamics is recalling SOFT-VU KUMPE 5F X 65CM angiographic catheters (595 boxes nationwide) because inner pouch labels may show information for a different catheter model while shelf-box labels are correct.

    Product
    SOFT-VU KUMPE 5F X 65CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732701
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1519-2024·2024-08-07

    NaturesPlus Testosterone Supplement Recalled for Missing Ingredient and Incorrect Formulation

    Natural Organics is recalling NaturesPlus ULTRA T-MALE due to incorrect formulation: the product is missing the ingredient TongKat Ali and contains additional Rhodiola Rosea. No illnesses have been reported.

    Product
    NaturesPlus ULTRA T-MALE Maximum Strength Testosterone Boost for Men 60 Bi-layer Tablets
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2453-2024·2024-08-07

    SOFT-VU KUMPE Diagnostic Catheter Recalled for Mislabeled Inner Pouch

    Angiodynamics recalls SOFT-VU KUMPE diagnostic catheters because inner pouch labels may show incorrect catheter length information, while the outer box label is accurate. 519 boxes distributed nationwide.

    Product
    SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0621-2024·2024-08-07

    Prescription azelaic acid gel recalled for manufacturing process deviations

    Glenmark Pharmaceuticals recalls azelaic acid gel 15% nationwide due to manufacturing process deviations. Patients should consult their healthcare provider about their prescription.

    Product
    AZELAIC ACID — AZELAIC ACID (AZELAIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0623-2024·2024-08-07

    Ciprofloxacin Ophthalmic Solution Recalled Due to Defective Container

    FDC Limited is recalling 66,528 bottles of Ciprofloxacin ophthalmic solution USP 0.3% due to a manufacturing defect in the container cap that prevents access to the medication. All affected bottles were distributed nationwide.

    Product
    CIPROFLOXACIN — CIPROFLOXACIN (CIPROFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1520-2024·2024-08-07

    NaturesPlus T-MALE Testosterone Support Supplement Recalled for Ingredient Mismatch

    NaturesPlus T-MALE liquid supplement is being recalled because the product is missing the key ingredient TongKat Ali and contains an additional ingredient, Rhodiola Rosea, that should not be present.

    Product
    NaturesPlus T-MALE Liquid Testosterone Support for Men 8 OZ Berry and 30 OZ Berry
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V283000·2024-08-04

    2023 Ford Ranger Loose Lug Nuts Recall — Wheel Detachment Risk

    Ford is recalling 1,434 2023 Ranger vehicles due to improperly tightened lug nuts on driver-side wheels. Loose lug nuts may cause wheel detachment while driving, increasing crash risk.

    Product
    FORD — 2023 FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V282000·2024-08-04

    International CV Brake Pressure Switch Fire Risk Recall

    Navistar is recalling 2017-2023 International CV trucks for a brake pressure switch assembly defect that may leak brake fluid and cause an electrical short-circuit, increasing fire risk while driving or parked.

    Product
    INTERNATIONAL — 2018 INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V189000·2024-08-03

    2024 Ford Bronco Rear Door Latch May Open When Child Safety Lock Is On

    Ford is recalling certain 2023-2024 Bronco 4-door vehicles because the left-side rear door may open from inside even when the child safety lock is engaged, increasing the risk of injury.

    Product
    FORD — 2024 FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V187000·2024-08-03

    Ford Bronco Sport and Escape fuel injector fire risk recall

    Ford is recalling the 2022-2023 Bronco Sport and 2022 Escape with 1.5L engines due to a fuel injector that may crack and leak fuel, creating a fire risk in the engine compartment.

    Product
    FORD — 2022 FORD BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V185000·2024-08-03

    2024 Ford Maverick Fuel Tank Defect Increases Fire Risk

    Ford is recalling certain 2024 Maverick vehicles because the fuel tanks may have an open pinch joint that allows fuel to leak. In the presence of an ignition source, a fuel leak increases the risk of vehicle fire.

    Product
    FORD — 2024 FORD MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V191000·2024-08-03

    Genesis vehicles turbocharger oil feed pipe deterioration recall

    Hyundai is recalling certain Genesis G70, G80, and G90 vehicles with 3.3-liter turbocharged engines because the left turbocharger oil feed pipe may deteriorate and leak oil, increasing the risk of engine compartment fire. Hyundai will replace the affected pipe free of charge.

    Product
    GENESIS — 2020 GENESIS G90
    Category
    Vehicle
    Distribution
    Distributed nationwide