The Recall Desk

State

North Dakota product recalls

20,322 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.

14226–14250 of 20322

  • HighFDA (Devices)·Z-1079-2023·2023-02-15

    Sterile Procedural Trays Recalled for Potential Blade Puncture of Packaging

    Medline Industries is recalling multiple sterile procedural trays because blades within the kits can potentially puncture the outer foil packaging, compromising sterility. The recall affects approximately 215,456 units distributed worldwide.

    Product
    Sterile Procedural Trays, labeled as the following: a. BASIN SET-UP PACK b. LAP CHOLE CDS c. MAJOR CDS d. UROLOGY MINOR CDS e. UROLOGY MAJOR CDS f. SINGLE BASIC CDS g. ORGAN RECOVERY CDS h. GENERAL ABD CDS i. BURN CDS j. MINOR k. MAJOR VASCULAR l. BASIC CORE CDS m. ROBOTIC PROC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1068-2023·2023-02-15

    Sterile Procedural Trays Recalled Due to Blade Package Puncture Risk

    Medline sterile procedural trays are recalled because sterile blades within the kits can puncture the outer foil packaging, potentially compromising sterility. 622 cases (1,619 units) have been distributed worldwide.

    Product
    Sterile Procedural Trays, labeled as the following: a. PORT/TRACH INSERTION CDS-3 b. RESIDENT DERM SURG PACK c. THROMBECTOMY PACK-LF d. AV FISTULA PACK e. AV SHUNT PACK-LF f. RR-VP SHUNT PACK-LF g. VEIN HARVESTING PACK-LF h. AV FISTULA PACK-LF i. PK, GEN-BARIATRIC j.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1074-2023·2023-02-15

    Sterile Procedural Trays Recalled Due to Blade Packaging Puncture Hazard

    Medline Industries is recalling multiple sterile procedural trays because blades within the kits can puncture the outer foil packaging. The products were distributed worldwide.

    Product
    Sterile Procedural Trays, labeled as the following: a. LAPAROTOMY CDS-LF b. LAPAROSCOPY CDS-LF c. BASIC LAPAROSCOPY CDS d. LAPAROSCOPY CDS-LF e. GENERAL LAPAROSCOPY PROCEDURE f. LAP CHOLE CDS g. COLO-RECTAL CDS-LF h. MAJOR PROCEDURE-LF i. HYPOSPADIUS CDS j. LAPAROSCOPY-GENERAL k
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1076-2023·2023-02-15

    Sterile Procedural Trays Recalled Due to Blade Puncture Risk

    Medline Industries is recalling sterile procedural trays (ENDOSCOPY-LF and SEPTO/ENDO) because sterile blades may puncture the outer foil layer of the sterile packaging. The recall affects units distributed nationwide and internationally.

    Product
    Sterile Procedural Trays, labeled as the following: a. ENDOSCOPY-LF b. SEPTO/ENDO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1082-2023·2023-02-15

    Sterile Procedural Trays recalled due to potential sterile packaging puncture

    Medline Industries is recalling Sterile Procedural Trays (IM NAIL) because sterile blades may puncture the outer foil layer of sterile packaging, potentially compromising sterility. No illnesses or injuries have been reported.

    Product
    Sterile Procedural Trays, labeled as the following: IM NAIL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1087-2023·2023-02-15

    Medline Procedural Trays Recalled for Blade Packaging Risk

    Medline Industries is recalling Ambulatory Mini Pack sterile procedural trays because blades within the kits may puncture the outer sterile packaging, potentially compromising sterility.

    Product
    Sterile Procedural Trays, labeled as the following: AMBULATORY MINI PACK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1091-2023·2023-02-15

    Sterile Surgical Trays Recalled for Potential Sterile Packaging Puncture

    Medline Industries recalls sterile surgical procedural trays because blades within the kits could puncture the sterile outer packaging, potentially compromising sterility during surgical use.

    Product
    Sterile Procedural Trays, labeled as the following: a. GYN-URO LAPSCP CDS-LF b. ROBOTIC CDS c. GYN LAPAROSCOPY CDS-LF d. GYN LAPAROSCOPY e. GYN LAPAROSCOPY CDS f. UNIVERSAL ROBOTIC ORLANDO g. GYN ROBOTIC CDS h. GYN LAPAROSCOPY CDS-1 i. CUH GYN LAPAROSCOPY CDS j. CUH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0265-2023·2023-02-15

    Akorn Atropine Sulfate Eye Solution Recalled for Failed Stability Testing

    Akorn is recalling 45,117 bottles of Atropine Sulfate Ophthalmic Solution because stability testing found viscosity measurements out of specification. The affected product should not be used.

    Product
    Atropine Sulfate Ophthalmic Solution, USP 1%, For Topical Application To The Eye, 2 mL bottle, Sterile, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. NDC: 17478-215-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1052-2023·2023-02-15

    NuVasive Pulse III Multimodality System remote monitoring connection failure

    An incorrect security key prevents the NuVasive Pulse III system from connecting to remote monitoring during spinal, thoracic, and extremity surgeries. Affected facilities should contact NuVasive for corrective action.

    Product
    NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V928000·2023-02-12

    2022 Ford Bronco Airbag Sensors May Not Secure Properly

    Ford is recalling certain 2022 and 2021 Bronco vehicles because the side impact sensors may not be properly secured. This could cause airbags to deploy unintentionally or fail to deploy in a crash, increasing injury risk.

    Product
    FORD — 2022 FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V923000·2023-02-12

    2022-2023 Chevrolet Malibu Recalled for Defective Front Impact Bar Weld

    General Motors is recalling certain 2022-2023 Chevrolet Malibu vehicles with improperly welded front impact bars. The structural defect may prevent crash sensors from working correctly, increasing the risk of injury in a crash.

    Product
    CHEVROLET — 2022 CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V735000·2023-02-11

    2023-2024 Honda Pilot steering rack defect may cause loss of steering control

    Honda is recalling certain 2023-2024 Pilot vehicles due to a loose ball bearing in the steering rack gearbox assembly. This defect can result in loss of steering control or steering lock-up, increasing crash risk.

    Product
    HONDA — 2023 HONDA PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V665000·2023-02-10

    2024 Holiday Rambler Invicta Motorhome Griddle Fire Hazard Recall

    REV Recreation Group is recalling certain 2024 Holiday Rambler Invicta motorhomes. The exterior griddle may be stowed while still connected to the LP gas line, creating a fire risk.

    Product
    HOLIDAY RAMBLER — 2024 HOLIDAY RAMBLER INVICTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23116·2023-02-09

    Ovation Protégé Equestrian Helmets Recalled for Impact Injury Hazard

    English Riding Supply is recalling about 49,300 Ovation Protégé equestrian helmets because they fail to meet safety impact standards. Riders who fall face an injury risk.

    Product
    Equestrian helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23723·2023-02-09

    Model Year 2023 Can-Am Side-by-Side Vehicles Recalled for Fire Hazard

    BRP is recalling about 3,310 Model Year 2023 Can-Am side-by-side vehicles because a defective fuel hose assembly could leak fuel and create a fire hazard. Consumers should stop using the vehicles and contact a Can-Am dealer for a free repair.

    Product
    Model Year 2023 Can-Am side-by-side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V686000·2023-02-09

    2022 Ford F-150 Parking Light Flickering Defect Recall

    Ford is recalling 2022 F-150 trucks and 2022-2023 Bronco Sport vehicles due to a lighting control module defect causing parking light flickering when headlights are activated. The flickering reduces visibility and increases crash risk.

    Product
    FORD — 2022 FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V685000·2023-02-09

    2022 Ford Ranger Loose Fuel Line Connection Increases Fire Risk

    Ford is recalling certain 2022 Ranger and Explorer models with 2.3L engines due to potentially loose fuel line connections. An improperly tightened connection may result in a fuel leak, increasing the risk of fire.

    Product
    FORD — 2022 FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23118·2023-02-09

    IKEA ODGER Swivel Chairs Recalled Due to Leg Base Breakage and Fall Risk

    IKEA is recalling about 12,000 ODGER Swivel Chairs in anthracite because the leg base can break, creating a fall hazard. Four reports of leg base breaking have been received, including two reports of consumer injuries from falls.

    Product
    IKEA ODGER Swivel Chairs, Anthracite
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23725·2023-02-09

    LiftMaster myQ Garage Door Control Panels Recalled for Entrapment Hazard

    Chamberlain Group is recalling about 96,400 LiftMaster myQ garage door control panels because the secondary entrapment protection system can fail, allowing the garage door to close even when an obstruction is present. No injuries have been reported in the U.S.

    Product
    LiftMaster myQ Garage Door Control Panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23726·2023-02-09

    E-Z-GO Personal Transportation Vehicles Recalled for Fire Hazard

    Textron Specialized Vehicles is recalling about 143,000 E-Z-GO personal transportation vehicles because the electronic board powering the USB port can overheat and ignite, creating a fire hazard. Consumers should stop using the vehicles immediately and contact Textron for a free repair.

    Product
    E-Z-GO Personal Transportation Vehicles (PTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V687000·2023-02-09

    2022 Volkswagen Taos Engine Stall Software Safety Recall

    Volkswagen is recalling certain 2022 Taos vehicles with all-wheel drive due to engine control unit software that may cause engine stall when coming to a stop, increasing crash risk. Dealers will provide free software updates.

    Product
    VOLKSWAGEN — 2022 VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23117·2023-02-09

    Skip Hop Silver Lining Cloud Activity Gyms Recalled for Choking Hazard

    Skip Hop is recalling Silver Lining Cloud Activity Gyms because raindrops attached to the included cloud toy can detach and pose a choking hazard to children. No injuries have been reported.

    Product
    Silver Lining Cloud Activity Gyms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23724·2023-02-09

    WeeSprout Baby Sleep Sacks Recalled Due to Choking Hazard

    WeeSprout baby sleep sacks are being recalled because the zipper can detach, posing a choking hazard to infants. The company has received 17 reports of zipper detachment but no injuries have been reported.

    Product
    Baby Sleep Sacks
    Category
    Consumer Product
    Distribution
    Distributed nationwide