The Recall Desk

State

North Dakota product recalls

20,305 recalls have nationwide distribution and so reach North Dakota. 0 additional recalls listed North Dakota specifically in their distribution scope.

About recalls in North Dakota

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 North Dakota 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.

12276–12300 of 20305

  • HighNHTSA·22V018000·2023-08-01

    2021-2022 Heartland RVs Recalled for Tire Belt Separation Risk

    Certain 2021-2022 Heartland Cyclone, Fuel, Gravity, and Road Warrior vehicles with Sailun tires may experience belt separation, risking loss of vehicle control. Dealers will replace affected tires at no cost.

    Product
    HEARTLAND — 2022 HEARTLAND CYCLONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23776·2023-07-27

    Sky Wheels Play Component Recalled for Fall Hazard

    Soft Play is recalling about 3,500 Sky Wheels play components because the wheels can detach from the overhead rail, causing a fall hazard and risk of injury to children. The company has received 15 reports of detachment, including three reported injuries involving scalp lacerations.

    Product
    Sky Wheels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23249·2023-07-27

    True Fitness Showrunner II Consoles Recalled for Fire Hazard

    True Fitness is recalling about 600 Showrunner II Consoles sold with fitness equipment due to a fire hazard from an exposed wireless charging board. One fire has been reported with no injuries.

    Product
    Showrunner II Consoles, with included wireless phone chargers, sold with fitness equipment
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23777·2023-07-27

    GAF Energy Timberline Solar Energy Shingles recalled due to fire hazard

    GAF Energy is recalling about 2,100 Timberline Solar Energy Shingles (TLS-1) due to electrical component malfunction that poses a fire hazard. One fire and five thermal incidents resulting in property damage have been reported, with no injuries.

    Product
    Timberline Solar Energy Shingles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2016-2023·2023-07-26

    Olympus Bronchovideoscope Recalled for Endobronchial Combustion Risk

    Olympus is recalling 17,609 bronchovideoscope units nationwide due to complaints of endobronchial combustion during therapeutic laser procedures, which poses a fire and burn risk to patients.

    Product
    Olympus EVIS EXERA II BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-P180, BF-Q180, BF-Q180-AC, BF-1T180, BF-1TQ180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1261-2023·2023-07-26

    Frozen Cherries Recalled Due to Potential Listeria Contamination

    SunOpta Grains and Foods Inc. is recalling frozen cherries sold under Great Value, Good & Gather, and Best Choice brands nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.

    Product
    Cherries packaged under the following brands and sizes: 1. Great Value Dark Sweet Cherries, Pitted. Net Wt 16 oz (1 lb) 454g, UPC 0 78742-11209 1. Keep Frozen. Distributed by: Walmart Inc., Bentonville, AR 72716 2. Good & Gather Dark Sweet Whole Pitted Cherries. Net
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1267-2023·2023-07-26

    365 Whole Foods Organic Tropical Fruit Medley recalled due to Listeria contamination risk

    365 Whole Foods Market Organic Tropical Fruit Medley is recalled nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume this product.

    Product
    365 Whole Foods Market Organic Tropical Fruit Medley. Strawberries, Mangoes, Bannas & Pineapples. Net Wt 32 oz (2 lb) 907g. UPC 0 99482-45715 0. Keep Frozen. Distributed by: Whole Foods Market, Austin, TX 78703
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1254-2023·2023-07-26

    Trader Joe's Organic Tropical Fruit Blend recalled for potential Listeria contamination

    Trader Joe's Organic Tropical Fruit Blend is recalled due to potential contamination with Listeria monocytogenes from pineapple ingredients. The 16 oz. bags were distributed nationwide.

    Product
    Trader Joe s Organic Tropical Fruit Blend Pineapple, Banana, Strawberry, Mango, SKU #051191, packaged in pillow bags. Each case consists of 24 bags and each bag is 16 oz. UPC on retail bag: 00511919
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1269-2023·2023-07-26

    Frozen Mixed Fruit Blend Recalled for Potential Listeria Contamination

    SunOpta's Good & Gather brand frozen mixed fruit blend is recalled nationwide due to potential Listeria monocytogenes contamination. Affected consumers should not consume this product and should return it to the retailer.

    Product
    Good & Gather Mixed Fruit Blend Pineapple Chunks, Sliced Strawberries, Mango Chunks & Sliced Peaches. Net Wt 48 oz (3lb) 1.36kg. UPC 0 85239-04821 4. Keep Frozen. Dist. By Target Corp, Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2114-2023·2023-07-26

    Abiomed Impella 5.5 pump recalled due to impeller blade damage risk

    Abiomed is recalling the Impella 5.5 with SmartAssist pump due to a risk of impeller blade destruction when used with aortic valve replacement devices. Damage can result in low blood flow and systemic embolization, where broken pump pieces may enter the bloodstream.

    Product
    Impella 5.5 with SmartAssist intravascular micro axial blood pump, Product Numbers 0550-0008 and 1000100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1265-2023·2023-07-26

    Frozen Triple Berry Blend Recalled for Potential Listeria Contamination

    Good & Gather Triple Berry Blend, sold at Target, is being recalled nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the affected product.

    Product
    Good & Gather Triple Berry Blend. Blueberries, Blackberries, & Red Raspberries. Net Wt 48 oz (3lb) 1.36kg, UPC 0 85239-04806 1. Keep Frozen. Dist By Target Corp. Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1255-2023·2023-07-26

    Frozen Pineapple Products Recalled Due to Listeria Contamination

    Scenic Fruit Company recalls Cadia and Trader Joe's frozen pineapple products due to potential Listeria monocytogenes contamination. Consumers should not consume the recalled items.

    Product
    Cadia - Organic Pineapple Frozen Fruit, packaged in stand-up pouch, net wt. 10oz. Each case consists of 12 bags. Product of Mexico. UPC on Retail Bag: 815369014540 UPC on Case: 10815369014547 Cadia FS - Organic Frozen Pineapple Chunks, net wt. 5lbs. Each case consists of 4
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2111-2023·2023-07-26

    Impella 2.5 blood pump recalled due to impeller blade damage risk

    Impella 2.5 intravascular blood pumps may experience unintended interaction with aortic valve replacement stents, damaging impeller blades and reducing blood flow. Fragments may circulate through the bloodstream.

    Product
    Impella 2.5 intravascular micro axial blood pump, Product Number 005042
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2015-2023·2023-07-26

    Olympus BRONCHOVIDEOSCOPE Model BF-Q170 Recalled Due to Combustion Risk

    Olympus BRONCHOVIDEOSCOPE Model BF-Q170 is recalled nationally due to complaints of endobronchial combustion during therapeutic laser procedures, classified as FDA Class I.

    Product
    Olympus BRONCHOVIDEOSCOPE, Model Numbers BF-Q170
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2013-2023·2023-07-26

    Olympus Bronchoscope Recall: Risk of Combustion During Laser Procedures

    Olympus is recalling 9 bronchoscopes (Models BF-P150 and BF-1T150) due to complaints of endobronchial combustion during therapeutic laser procedures. The defect could cause fire and serious burn injuries.

    Product
    Olympus BRONCHOVIDEOSCOPE BF Type, Model Numbers BF-P150, BF-1T150
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2149-2023·2023-07-26

    Cardiosave Hybrid IABP may fail to charge batteries, interrupting therapy

    The Cardiosave Hybrid Intra-Aortic Balloon Pump may lose the ability to charge batteries in one or both bay slots, potentially interrupting critical therapy if disconnected from AC power. Low battery alarms may alert users before therapy is interrupted.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0998-00-0800-34 0998-00-0800-35 0998-00-0800-45 0998-00-0800-52 0998-00-0800-53 0998-00-0800-55 0998-00-0800-65 0998-UC-0800-31* 0998-UC-0800-33* 0998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2113-2023·2023-07-26

    Impella LD cardiac pump recalled for impeller damage and embolization risk

    Abiomed recalls Impella LD blood pumps due to potential interaction with aortic valve replacement devices that can damage the pump impeller and cause blood clots. Patients with these devices should contact their healthcare provider.

    Product
    Impella LD intravascular micro axial blood pump, Product Number 005082
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1259-2023·2023-07-26

    Good & Gather Frozen Blueberries Recalled for Potential Listeria Contamination

    Target's Good & Gather frozen blueberries are being recalled nationwide due to potential Listeria monocytogenes contamination affecting approximately 3,894 cases.

    Product
    Good & Gather Blueberries. Net Wt 48 oz (3lb) 1.36kg UPC 0 85239-04813 9. Keep Frozen. Distributed by Target Corporation Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1260-2023·2023-07-26

    365 Whole Foods Organic Blackberries Recalled for Potential Listeria Monocytogenes

    Whole Foods Market is recalling 365 brand organic blackberries due to potential Listeria monocytogenes contamination. The frozen fruit was distributed nationwide.

    Product
    365 Whole Foods Market Organic Blackberries. Net Wt 10 oz (284g), UPC 0 99482-40605 9. Keep Frozen. Distributed by: Whole Foods Market, Austin, TX 78703
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1263-2023·2023-07-26

    Great Value Mixed Fruit Recalled for Potential Listeria Contamination

    Walmart's Great Value Mixed Fruit is recalled for potential Listeria monocytogenes contamination. The FDA issued a Class I recall affecting approximately 70,360 cases distributed nationwide.

    Product
    Great Value Mixed Fruit. Pineppple, Strawberries, Peaches and Mango. Net Wt 16 oz (1 lb) 454g, UPC 0 78742-02551 3. Keep Frozen. Distributed by: Walmart Inc., Bentonville, AR 72716
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1262-2023·2023-07-26

    Good & Gather Organic Frozen Cherries & Berries Recalled for Listeria Risk

    SunOpta Grains and Foods is recalling Good & Gather Organic frozen cherries and berries distributed nationwide by Target due to potential Listeria monocytogenes contamination.

    Product
    Good & Gather Organic cherries & berries fruit blend. Blueberries, dark sweet pitted cherries, tart pitted cherries & Strawberry slices. Net Wt 32 oz (2 lb) 907g, UPC 0 85239-04782 8. Keep Frozen. Distributed by Target Corporation Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1266-2023·2023-07-26

    Good & Gather Mango Strawberry Blend recalled for Listeria contamination risk

    Target's Good & Gather Mango Strawberry Blend is being recalled nationwide due to potential Listeria monocytogenes contamination. Listeria can cause serious illness.

    Product
    Good & Gather Mango Strawberry Blend. Whole Strawberries, Mango chunks & Pineapple Chunks. Net Wt 48 oz (3lb) 1.36kg, UPC 0 85239-04803 0. Keep Frozen. Dist. By Target Corp, Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2116-2023·2023-07-26

    Impella CP cardiac pump recalls due to motor housing interaction with stents

    Abiomed is recalling Impella CP with SmartAssist blood pumps due to risk of motor housing interaction with transcatheter aortic valve replacement devices, which can damage the pump's impeller blades and reduce blood flow.

    Product
    Impella CP with SmartAssist intravascular micro axial blood pump, Product Numbers 0048-0024, 0048-0045, 1000080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2152-2023·2023-07-26

    Cardiosave Rescue IABP Recalled Due to Unexpected Shutdown Risk

    Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to capacitor failures that may cause unexpected device shutdown. The devices may stop delivering therapy without warning.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2012-2023·2023-07-26

    Olympus Bronchofiberscope BF Type recalled for combustion risk during laser procedures

    Olympus bronchoscopes (Models BF-PE2 and BF-TE2) are recalled due to reports of combustion inside the airway during laser-assisted medical procedures. This is an FDA Class I recall.

    Product
    Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
    Category
    Medical Device
    Distribution
    Distributed nationwide