The Recall Desk

State

North Dakota product recalls

20,308 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.

13476–13500 of 20308

  • ModerateFDA (Devices)·Z-1430-2023·2023-05-03

    Caspar Cervical Retractor Basket Lids Recalled for Incorrect GTIN Labeling

    Aesculap Implant Systems recalls Caspar Cervical Retractor (CCR) Basket lids with incorrect GTIN labeling. The product bears GTIN #04046955299592 instead of the correct #04046955299607.

    Product
    Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and ME764 Casper Cervical Retractor (CCR) Basket Full System - Lid Only. A lid to a container intended to provide a suitable platform for placing/containing many medical/surgical/dental instruments. Note: The CCR basket
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0546-2023·2023-05-03

    DuPont Avicel PH-200 NF pharmaceutical ingredient recalled for conductivity specification failure

    DuPont is recalling Avicel PH-200 NF microcrystalline cellulose, a pharmaceutical ingredient, for failing conductivity specifications. The bulk ingredient was distributed to drug manufacturers in the USA and internationally.

    Product
    Avicel PH-200 NF, Microcrystalline Cellulose NF, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0551-2023·2023-05-03

    FDA Recalls Glimepiride Tablets for Manufacturing Deviations

    Northwind Pharmaceuticals is voluntarily recalling Glimepiride 2mg tablets distributed nationwide due to Good Manufacturing Practice (CGMP) deviations identified during manufacturing.

    Product
    GLIMEPIRIDE — GLIMEPIRIDE (GLIMEPIRIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0541-2023·2023-05-03

    CBD Metered Dose Inhaler Recalled for Marketing Without FDA Approval

    Wellness BioSciences is recalling its CBD Metered Dose Inhaler nationwide because it was marketed without an approved NDA/ANDA.

    Product
    CBD Metered Dose Inhaler (CBD) 5 mg Dose, 1 Metered Dose Inhaler, 100 Metered Sprays, Wellness BioSciences Rx
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0555-2023·2023-05-03

    FDA recalls Oxytocin product for low potency nationwide

    SCA Pharmaceuticals is recalling Oxytocin 30 units in 0.9% Sodium Chloride solution (73,312 containers) nationwide due to subpotency—product contains insufficient active ingredient.

    Product
    Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL, Rx Only, Single Dose Container, SCA Pharmaceuticals, Windsor, CT 06095, NDC# 70004-085-44
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0545-2023·2023-05-03

    FDA recalls Avicel PH-102 microcrystalline cellulose bulk ingredient for specification failure

    DuPont Nutrition is recalling Avicel PH-102 microcrystalline cellulose due to conductivity specification failures in 14 batches distributed across the USA and internationally.

    Product
    Avicel PH-102 NF, Microcrystalline Cellulose NF, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V091000·2023-05-02

    2022 Chevrolet Corvette rear driveshaft defect may cause loss of power

    General Motors is recalling 2021-2022 Chevrolet Corvette vehicles whose rear half-shaft assemblies may be missing ball bearings. This can cause sudden loss of drive power, increasing crash risk.

    Product
    CHEVROLET — 2022 CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V031000·2023-05-01

    2021 BMW X5, X6, X7 Steering Column Defect Recall

    BMW is recalling certain 2021 X5, X6, and X7 models due to a defect in the steering column shaft universal joint that may not be tightened to specifications, potentially affecting vehicle handling and control.

    Product
    BMW — 2021 BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V034000·2023-05-01

    2021 Mercedes-Benz ISOFIX Bracket May Be Missing From Child Restraint Anchor

    Mercedes-Benz is recalling certain 2021 A220, A35 AMG, and CLA250 vehicles because the ISOFIX child seat anchoring bracket on the right-rear seat may be missing the right-side anchoring bar, preventing proper restraint of child car seats.

    Product
    MERCEDES-BENZ — 2021 MERCEDES-BENZ AMG A35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V015000·2023-05-01

    2022 Keystone Alpine RV Exterior Ladder May Detach from Rear Wall

    Keystone RV Company is recalling certain 2022 Alpine and Avalanche vehicles due to improperly secured exterior ladders that may detach while in use, creating a risk of injury.

    Product
    KEYSTONE — 2022 KEYSTONE ALPINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23749·2023-04-27

    Ejoyous Pool Drain Covers Recalled for Entrapment Hazard

    Ejoyous pool drain covers sold online do not meet Virginia Graeme Baker Pool and Spa Safety Act standards and pose an entrapment hazard to swimmers and bathers.

    Product
    Ejoyous pool drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23192·2023-04-27

    Easter Bunny and Butterfly Jewel Necklaces Recalled for High Cadmium

    Creative Education of Canada is recalling about 4,300 Easter Bunny and Boutique Butterfly Jewel Necklaces sold nationwide and online from January through March 2023 due to high levels of cadmium, which is toxic if ingested by children.

    Product
    Easter Bunny and Boutique Butterfly Jewel Necklaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23750·2023-04-27

    Pool Drain Covers Recalled for Entrapment Hazard

    Vijayli-US is recalling about 116 round pool drain covers sold online that do not meet Virginia Graeme Baker Pool and Spa Safety Act standards, posing an entrapment hazard to swimmers and bathers.

    Product
    Pool drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23191·2023-04-27

    EGL Motor ACE Youth ATVs Fail Safety Standards; Risk of Injury or Death

    EGL Motor is recalling about 4,000 ACE-branded youth all-terrain vehicles (ATVs) that fail federal safety standards. The K125 and C125 models exceed maximum speed limits, and the T125 and C125 models have faulty parking brakes, posing risks of high-speed crashes and collisions.

    Product
    EGL Motor ACE-branded Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23189·2023-04-27

    Vornado Recalls Travel Steam Irons for Fire, Burn, and Shock Hazards

    Vornado is recalling approximately 317,000 Steamfast and Brookstone travel steam irons because the power cord can become damaged near the bushing, creating fire, burn, and electrical shock hazards. No injuries have been reported.

    Product
    Steamfast Home & Away Travel Steam Irons and Brookstone Steam Bug Travel Steam Irons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23748·2023-04-27

    Pool and Spa Drain Covers Recalled for Entrapment Hazard Violation

    Pickloud-US has recalled approximately 100 round pool and spa drain covers sold on Amazon because they do not meet entrapment protection standards under the Virginia Graeme Baker Pool and Spa Safety Act, posing an entrapment hazard to swimmers and bathers.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23190·2023-04-27

    Black Diamond Recon LT Avalanche Transceivers Recalled for Communication Loss Risk

    Black Diamond is recalling about 1,550 Recon LT avalanche transceivers because they can unexpectedly enter search mode due to beacon interference, potentially failing to transmit a skier's position during an avalanche rescue.

    Product
    Recon LT Avalanche Transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23194·2023-04-27

    Diamond Visions Recalls Screaming Plush Monkey Toys for Choking Hazard

    Diamond Visions is recalling about 6,000 Screaming Plush Monkey Toys because the eyes can detach, creating a choking hazard for children. No injuries have been reported.

    Product
    Screaming Plush Monkey Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0738-2023·2023-04-26

    Sheila G's Gluten Free Reese's Pieces Brownie Brittle recalled for undeclared wheat

    Sheila G's Gluten Free Reese's Pieces Brownie Brittle (4 oz bags, UPC 711747 011562) is being recalled because the product may contain undeclared wheat despite its gluten-free label, creating a risk for consumers with celiac disease or wheat allergies.

    Product
    Sheila G's Gluten Free Reese's Pieces Brownie Brittle, 4 oz bag (Retail bag UPC 711747 011562)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1357-2023·2023-04-26

    Shiley Adult Flexible Tracheostomy Tubes Recalled Due to Undersized Connectors

    Covidien is recalling Shiley Adult Flexible Tracheostomy Tubes due to undersized connectors that create loose connections with 15mm respiratory circuit components. Unsecure connections could cause respiratory failure, difficulty breathing, treatment delays, or serious injury.

    Product
    Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner Cannula (REF, Product Description): 10CN10H, 10.0MM SHILEY CUFFED TRACH CAN; 10CN10R, 10.0MM ADT FLEX TRACH W TG CUFF; 10UN10A, 10.0MM UNCUFF TRACH TUBE X1;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1411-2023·2023-04-26

    Spinal Implant Screws Recalled for Defective Titanium Material

    Medtronic is recalling INFINITY spinal implant screws manufactured with incorrect titanium material. The defect reduces the screw's gripping strength, risking implant performance in critical spinal fusion surgery.

    Product
    INFINITY Occipitocervical Upper Thoracic System, PARTIALLY THREADED MULTI AXIAL SCREW, Size: 4.0mm x 22mm, REF 360PT4022; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unctio
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1393-2023·2023-04-26

    Smith & Nephew Knee Implant Component Mispack: Wrong Size Distributed

    Smith & Nephew is recalling 12 JOURNEY II UNI Tibia Insert components due to a manufacturing mispack. Some boxes incorrectly contain a different size component.

    Product
    JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1418-2023·2023-04-26

    Olympus Single-Use Endoscopic Clip Fixing Device Recalled for Deployment Failure

    Olympus is recalling single-use rotatable clip fixing devices used in endoscopy procedures. The clips may fail to deploy from the tube sheath during use.

    Product
    Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable, 165cm long, 2.8 scope channel, standard clip Model HX 201UR 135 - Rotatable, 230 cm long, 2.8 scope channel, standard clip Model HX 201UR 135L - Rotatable, 230 cm long, 2.8 mm scope channel, Long clip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0733-2023·2023-04-26

    Dietary Supplement with Unapproved COVID-19 Treatment Claims Recalled

    Natural Solutions Foundation is recalling a colloidal silver dietary supplement labeled to treat COVID-19. The product violates FDA regulations prohibiting disease claims on dietary supplements.

    Product
    Dr. Rima Recommends The Silver Solution Immune System Support Dietary Supplement Nano Silver 10 ppm 16 fl. oz. (473 ml)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1410-2023·2023-04-26

    Medtronic INFINITY Spinal Fusion Screws Recalled for Material Defect

    Medtronic is recalling 10 units of INFINITY Multi-Axial Screws distributed in the US and Canada because incorrect titanium material reduces gripping strength in affected lots.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 32mm, REF 3604532; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
    Category
    Medical Device
    Distribution
    Distributed nationwide