The Recall Desk

State

North Dakota product recalls

20,364 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.

15501–15525 of 20364

  • LowFDA (Devices)·Z-1798-2022·2022-10-05

    AquaGuard Wound Dressing Recall Due to Facility Temperature Excursions

    TIDI Products AquaGuard wound dressings received June–September 2021 were exposed to elevated storage temperatures that may have impacted product effectiveness. The FDA states adverse health consequences are unlikely.

    Product
    a. TIDI PRODUCTS, LLC AquaGuard DRESSING, AQUA GUARD MOISTR 7X7 (5/PK) 9CENCO Catalog #68751510104. b. TIDI PRODUCTS, LLC AquaGuard DRESSING, AQUA GUARD MOISTR BARR 10X12 (5/BX) Catalog #68751510105
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V286000·2022-10-04

    2021 Nissan Rogue brake caliper defect poses crash risk

    Nissan is recalling 2021 Rogue vehicles because the rear brake calipers may be missing an internal bushing, causing brake fluid to leak and reducing braking performance, increasing the risk of a crash.

    Product
    NISSAN — 2021 NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V280000·2022-10-04

    2020-2021 Dodge Durango Side Air Bag Fastener Recall

    Chrysler is recalling 2020-2021 Dodge Durango vehicles because the side curtain air bag fastener may be loose or missing. A loose fastener could cause incorrect air bag deployment, increasing injury risk.

    Product
    DODGE — 2020 DODGE DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V281000·2022-10-04

    International RH and LT trucks recalled for engine connecting rod failure

    Navistar is recalling certain 2019-2021 International LT and RH trucks due to wrist pin cracks that can cause connecting rod failure and engine stalls. Affected owners should contact their dealer for free repair.

    Product
    INTERNATIONAL — 2020 INTERNATIONAL RH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V101000·2022-10-02

    2021 Mazda Mazda3 and CX-30 tire air valve failure recall

    Mazda is recalling 2021 Mazda3 and CX-30 vehicles because air may leak from the tire air valve, potentially causing loss of vehicle control. Mazda will replace all tire air valves at no cost.

    Product
    MAZDA — 2021 MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V076000·2022-10-02

    2022 Thor Motor Coach Motorhomes Rear Ladder Installation Defect Recall

    Thor Motor Coach is recalling 2022 ACE, Freedom Traveler, Hurricane, and Windsport motorhomes. The rear ladder may have been installed on the wrong side, which could break while in use and cause injury.

    Product
    THOR MOTOR COACH — 2022 THOR MOTOR COACH ACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22235·2022-09-29

    Custom Elevator Residential Elevators Recalled for Child Entrapment Hazard

    Custom Elevator is recalling residential elevators due to a hazardous gap between the exterior landing door and interior car door that can trap young children. One child died from entrapment in July 2021.

    Product
    Residential elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·22234·2022-09-29

    Cambridge Elevating Residential Elevators Recalled for Child Entrapment Hazard

    Cambridge Elevating residential elevators may have a hazardous gap between exterior and interior doors that can trap young children, posing a risk of serious injury or death when the elevator moves. About 1,700 units sold nationwide from 1991 through August 2022 are affected.

    Product
    Residential elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22779·2022-09-29

    E-Z-GO RXV Personal Transportation Vehicles Steering System Failure Recall

    Textron Specialized Vehicles recalled about 34,000 E-Z-GO RXV personal transportation vehicles (golf carts) because steering knuckles and A-arms can break during impact, causing loss of steering control and crash hazards.

    Product
    E-Z-GO RXV Personal Transportation Vehicles (PTV)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22232·2022-09-29

    North States Industries Recalls Toddleroo Rotating Cabinet Latches for Choking Risk

    North States Industries is recalling about 103,000 Toddleroo Rotating Cabinet Latches because the latching button can detach, posing a choking hazard to young children. The company has received 19 reports of the button dislodging, including one report of a child gagging.

    Product
    Toddleroo Rotating Cabinet Latches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22233·2022-09-29

    Children's Bowtie Hairclips Recalled for Excessive Lead Content

    BE Jewel Accessories is recalling about 1,200 children's bowtie hairclips sold nationwide because the crystals exceed federal lead content limits. Lead poses a toxicity risk if ingested by young children.

    Product
    Children's Bowtie Hairclips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22237·2022-09-29

    HyperJuice 130W USB-C Battery Packs Recalled for Fire Hazard

    Hyper Products is recalling HyperJuice 130W USB-C Battery Packs because they can overheat while charging and pose a fire hazard. Two reports of overheating have resulted in smoke, melting, and property damage.

    Product
    HyperJuice 130W USB-C Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22781·2022-09-29

    Yamaha Viking Off-Road Side-by-Side Vehicles Recalled for Brake Hazards

    Yamaha is recalling about 330 Model Year 2022 Viking Off-Road Side-by-Side vehicles because improperly installed rear brake lines can leak brake fluid and reduce vehicle control, creating crash and injury hazards.

    Product
    Yamaha Viking Off-Road Side-by-Side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22780·2022-09-29

    Rockgeist BarJam Brackets Recalled Due to Crack and Injury Hazards

    Rockgeist BarJam Brackets can crack or break during use, causing gear to fall from a moving bicycle and posing crash and injury hazards. About 420 units sold online from September 2021 through August 2022.

    Product
    BarJam Brackets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22778·2022-09-29

    Hillsdale Furniture Flynn Twin Full Bunk Beds recalled for entrapment hazard

    Hillsdale Furniture is recalling about 821 Flynn Twin Full Bunk Beds With Ladders due to a gap wider than 3.5 inches between the second rung and lower bunk frame that poses an entrapment hazard to children when the mattress is removed. No injuries have been reported.

    Product
    Flynn Twin Full Bunk Beds With Ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22236·2022-09-29

    HyperJuice Stackable GaN USB-C Chargers Recalled for Fire Hazard

    Hyper Products is recalling about 18,200 HyperJuice Stackable GaN USB-C Chargers (models HJ414 65W and HJ417 100W) because they can overheat and pose a fire hazard. No injuries have been reported.

    Product
    HyperJuice Stackable GaN USB-C Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1776-2022·2022-09-28

    FDA Recalls Grappler Suture Anchors Due to Potential Breakage Risk

    Paragon 28, Inc. is recalling Grappler Suture Anchors (REF: P44-110-3010-SK, Lot 5007499) due to risk that the anchor may break upon insertion, potentially leaving debris in patients and delaying surgery.

    Product
    Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1772-2022·2022-09-28

    Serological Test Positive Control Shows False Negative Results for Hepatitis B

    Randox Serology I Positive Control may test negative for Hepatitis B surface antigen (HBsAg) on certain analyzers despite being designed as a positive control, potentially affecting laboratory quality control procedures.

    Product
    The Randox Serology I Positive Control contains the following analytes in human based plasma: Anti HIV 1/2, Anti HTLV 1/2, Anti HCV, HBsAg, Anti HBc, and Anti Treponema pallidum IgG. The product is delivered as a liquid in a kit of 3 identical ready-to-use vials of 5 mL each.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1768-2022·2022-09-28

    Absorbable Gelatin Sponge Hemostat Recalled for Endotoxin Contamination

    GELITA MEDICAL GMBH recalled 3,596 boxes of ORCA FOAM hemostats after routine testing found higher than acceptable endotoxin levels. The surgical devices were distributed across the United States.

    Product
    ORCA FOAM STANDARD CUBE 10x10x10 mm, Absorbable Gelatin Sponge Hemostat, USP, REF ORCA FOAM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1765-2022·2022-09-28

    Medical device set recalled for potential sterility barrier compromise

    Maquet Medical Systems USA is recalling the BEQ-HLS 5050 (HLS Set Advanced 5.0) due to a potential breach in the sterility barrier that may compromise product sterility.

    Product
    BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70105.2797. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1769-2022·2022-09-28

    Hemodialysis Water Purification Unit Recalled for Missing EMI Shielding

    Fresenius is recalling 24 units of the AquaC UNO H reverse osmosis unit because internal ethernet cables lack ferrite cores, compromising electromagnetic compatibility in hemodialysis water purification systems.

    Product
    AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse osmosis unit intended for use with hemodialysis systems. Fresenius Part Number: 24-10VA-1 Vivonic Part Number: G02000970-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1764-2022·2022-09-28

    FDA expands recall: HLS Set Advanced 7.0 sterility barrier compromise

    Maquet Medical Systems USA has expanded a recall for HLS Set Advanced 7.0, a preconnected medical device used for heart and lung support, due to a potential breach in the sterility barrier that could compromise product sterility.

    Product
    BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70105.2794. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1766-2022·2022-09-28

    HLS Set Advanced Sterility Breach Recall for Cardiac Support Equipment

    Maquet Medical Systems USA is recalling HLS Set Advanced 5050 units due to a potential breach in the sterility barrier. The defect may result in compromised product sterility for this cardiac and respiratory support equipment.

    Product
    BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70106.9077. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1767-2022·2022-09-28

    Medical Device Recall: CARDIOHELP HLS Set Advanced Sterility Barrier Breach

    Maquet Medical Systems is expanding its recall of the CARDIOHELP HLS Set Advanced due to a potential breach in the sterility barrier that could compromise product sterility, affecting 6,871 US units and 18,670 worldwide.

    Product
    BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70106.9078. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide