The Recall Desk

State

North Dakota product recalls

73,198 recalls have nationwide distribution and so reach North Dakota. 2,924 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,924
Critical
265
Severe
729
Most recent
2026-09-23

Of the 2,924 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 729 (25%) are Severe.

Which agencies issued them

These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13701–13725 of 76122

  • CriticalFDA (Food)·F-0671-2024·2023-12-13

    Bix Produce Recalls Fruit Medley for Potential Salmonella Contamination

    FreshPoint Bix Produce Company is recalling 91 units of Bix Produce Item #12170 (5 lb. Chunk Melon w/Grape) distributed in Iowa, Minnesota, North Dakota, and Wisconsin due to potential Salmonella contamination.

    Product
    Bix Produce Item # 12170 Fruit, Chunk Melon w/Grape 5 lb. containing Cantaloupe, Honeydew, and Red Grapes. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0667-2024·2023-12-13

    Mixed Fruit Cups Recalled for Potential Salmonella Contamination

    FreshPoint Bix Produce Company is recalling Mixed Fruit Cups due to potential Salmonella contamination. The recall affects 432 units distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Mixed Fruit Cup, clam-shell container. Net Wt 5.75 oz (163g). Keep Refrigerated. Ingredients: Cantaloupe, Honeydew, Pineapple, Red Grapes. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117 Packaged with the following…
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0665-2024·2023-12-13

    FreshPoint Bix Produce Company Cantaloupe Recall Due to Salmonella Risk

    FreshPoint Bix Produce Company is recalling whole cantaloupes due to potential Salmonella contamination. The recall affects approximately 186 packs distributed across Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    FreshPoint Bix Produce Company, Whole Cantaloupe, Item 03143. 1/3 CT. 3 melons per container.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0669-2024·2023-12-13

    Mixed Fruit with Grapes Recalled for Potential Salmonella Contamination

    FreshPoint Bix Produce Company is recalling Mixed Fruit with Grapes products due to potential Salmonella contamination. Affected products were distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Bix Produce Mixed Fruit with Grapes products containing Cantaloupe, Honeydew, Pineapple, and Red Grapes. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117 Packaged with the following cuts and weights…
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0569-2024·2023-12-13

    Rudy brand whole cantaloupes recalled due to possible Salmonella contamination

    Sofia Produce, L.L.C. is recalling Rudy brand whole cantaloupes distributed across the United States and Canada due to possible Salmonella contamination.

    Product
    Whole cantaloupe, Brand name Rudy 11 count carton, 8 count carton, 9 count carton, 15 count carton d. Container description; Cardboard containers bearing the Rudy label. The Rudy brand cantaloupes also have an individual PLU sticker placed upon each cantaloupe, PLU sticker #…
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Drugs)·D-0144-2024·2023-12-13

    FDA Recalls SANDIMMUNE Oral Solution Due to Crystallization

    Novartis Pharmaceuticals is recalling SANDIMMUNE Oral Solution (cyclosporine 100 mg/mL) due to crystallization found in bottles. The affected lots were distributed nationwide.

    Product
    SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936. NDC 0078-0110-22
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0672-2024·2023-12-13

    Bix Produce Mixed Fruit Recall for Potential Salmonella Contamination

    FreshPoint Bix Produce Company is recalling Item #12217 mixed fruit (cantaloupe, pineapple, red grapes) due to potential Salmonella contamination. The product was distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Bix Produce Item # 12217 Fruit, Chk Cant/Pine 1/2" w/Grp, 5 lb. containing Cantaloupe, Pineapple, and Red Grapes. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0666-2024·2023-12-13

    FreshPoint Bix Produce Cantaloupe Fruit Cup Recalled for Potential Salmonella

    FreshPoint Bix Produce Company is recalling specific lots of Cantaloupe Fruit Cup (Item 19703) due to potential Salmonella contamination. Affected products were distributed to Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Cantaloupe Fruit Cup, Item 19703. clam-shell container. Net Wt 5.75 oz (163g). UPC 8 46709-00523 2. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0670-2024·2023-12-13

    Mixed Fruit Products Recalled for Potential Salmonella Contamination

    Bix Produce Mixed Fruit products containing cantaloupe, honeydew, and pineapple are recalled due to potential Salmonella contamination. Consumers should not consume the affected products.

    Product
    Bix Produce Mixed Fruit products containing Cantaloupe, Honeydew, and Pineapple. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117 Packaged with the following cuts and weights: 1. Item # 12192…
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0668-2024·2023-12-13

    Bix Produce Cut Cantaloupe Recalled for Potential Salmonella Contamination

    FreshPoint Bix Produce Company is recalling 1,355 units of cut cantaloupe products due to potential Salmonella contamination. Products were distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Bix Produce Cut Cantaloupe. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117 Packaged with the following cuts and weights: 1. Item # 12064, Fruit, Balls small Cantaloupe, 5 lb. 2. Item # 12070…
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·23V843000·2023-12-13

    Thomas Built Buses Recalls School Buses for Weak Rear Joint

    Daimler Trucks North America is recalling 321 Thomas Built school buses because a rear interior joint may be too weak, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2, SAF-T-LINER C2 JOULEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0355-2024·2023-12-13

    Infusomat Administration Sets recalled for tubing dimension defects

    B. Braun Infusomat Administration Sets may have incorrect tubing dimensions that cause false air-in-line alarms, interrupting medication delivery. The defects may prevent critical medications from reaching patients.

    Product
    Infusomat Administration Sets as listed below: 362031 Infusomat Space Pump Set with Caresite Injection Site; 362032 15 drops/mL, priming volume: 22mL, length: 119in, SafeLine; 362033 UNIV. 15 DR PUMP SET, 1.2 FIL, 2 CRSITE; 362034 Priming volume: 19mL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0420-2024·2023-12-13

    CARDIOHELP Emergency Drive Blockage May Impair Cardiac Blood Oxygenation

    The FDA is recalling CARDIOHELP Emergency Drive units due to potential blocking that impairs blood flow. Affected patients may experience ischemia and hypoxia from inappropriate low blood oxygen.

    Product
    CARDIOHELP Emergency Drive, Part Numbers 701048002 and 701076205. The CARDIOHELP System is a blood oxygenation and carbon dioxide removal system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0138-2024·2023-12-13

    Dietary supplement recalled for unapproved drug status and pharmaceutical contamination

    Dr. Ergin's SugarMD glucose support capsules are recalled nationwide because they were marketed without FDA approval and are contaminated with the pharmaceutical ingredients metformin and glyburide. Approximately 32,117 units were distributed in the U.S.

    Product
    Dr. Ergin's SugarMD, ADVANCED GLUCOSE SUPPORT Capsules, Dietary Supplement, helps support healthy glucose levels a) 60 count (UPC 1 95893 92767 8), b) 120 count (UPC 1 95893 54697 8), c) 180 count (UPC 1 95893 99957 6) bottles, Manufactured for SUGARMDS LLC, Port St. Lucie, FL…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0568-2024·2023-12-13

    Malichita whole cantaloupe recalled for possible Salmonella contamination

    Sofia Produce recalls Malichita brand whole cantaloupes for possible Salmonella contamination. The recall affects approximately 18,335 boxes distributed to multiple U.S. states and Canada.

    Product
    Whole cantaloupe, Brand name Malichita 11 count carton, 8 count carton, 9 count carton, 15 count carton d. Container description; Red Corrugated Paper Carton or Black Plastic RPC.
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-0474-2024·2023-12-13

    EVO VISIAN Intraocular Lenses recalled for potential specification defects

    Staar Surgical Company is recalling 9 EVO VISIAN intraocular lenses due to potential specification non-compliance. The affected devices were distributed to 40 US states.

    Product
    EVO VISIAN Implantable Collamer Lens, REF: VICMO12.6. Phakic Intraocular lens.
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0466-2024·2023-12-13

    EVO+VISIAN Implantable Collamer Lens Recalled for Specification Non-Compliance

    Staar Surgical recalls 51 EVO+VISIAN intraocular lenses due to potential specification non-compliance. Affected devices were distributed across multiple U.S. states.

    Product
    EVO+VISIAN Implantable Collamer Lens, REF: VICM5_13.2. Phakic Intraocular lens.
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Drugs)·D-0147-2024·2023-12-13

    ROPivacaine HCl Injection Bags Recalled Due to Leaking

    STAQ Pharma is recalling ROPivacaine HCl 0.2% injection bags nationwide due to leaking bags caused by manufacturing quality control failures. No illnesses or injuries have been reported.

    Product
    ROPivacaine HCl 0.2% PF in Sodium Chloride 1,000 mg/500 mL (2 mg per mL) Injection, 500 mL bags, Rx only, STAQ Pharma Inc. 14135 E 42nd Ave, Unit 50, Denver, Colorado 80239, NDC 73177-0109-26,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0501-2024·2023-12-13

    RANDOX Total Bilirubin Reagent Recall Due to Elevated Patient Results

    Randox is recalling RANDOX Total Bilirubin reagent because reports indicate elevated patient results when using plasma samples with this reagent.

    Product
    RANDOX Total Bilirubin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0426-2024·2023-12-13

    ProCuity Hospital Beds Missing Electrical Safety Test Data

    Stryker's ProCuity bed series model 3009 lacks required electrical safety test documentation, creating a risk of tissue burns or electrical shock. The beds are distributed across North America, Europe, and other regions.

    Product
    ProCuity bed series, model number 3009, item number: 3009PX-L-200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0495-2024·2023-12-13

    Integra Cranial Access Kit Recalled for Packaging Defect Compromising Sterility

    Integra LifeSciences is recalling 510 units of Cranial Access Kits due to a defect in outer packaging that can split spontaneously, compromising device sterility and increasing infection risk in neurosurgery.

    Product
    Integra Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7260
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0504-2024·2023-12-13

    Medical Catheter Sets Recalled Due to Bonding Material Defect

    CooperSurgical H/S Catheter Sets may have defective bonding material causing component detachment or leakage. The sets are used in hysterosalpingography procedures to detect uterine abnormalities.

    Product
    CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: 61-4005S For administering contrast media during Hysterosalpingography or Hysterosonography procedures to detect uterine pathology such as polyps, fibroids, adhesions or endometrial thickening, and/or patency…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0494-2024·2023-12-13

    Integra Cranial Access Kit Packaging Defect Compromises Sterility

    Integra LifeSciences is recalling 180 Cranial Access Kits due to a packaging defect that can cause splits, compromising the sterility of the surgical device.

    Product
    Integra¿ Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7280
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0499-2024·2023-12-13

    Cranial Access Kit Packaging Defect May Compromise Sterility

    Integra LifeSciences is recalling a cranial access kit due to a packaging defect that can cause the sterile outer packaging to split without additional force, potentially compromising device sterility.

    Product
    Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: 31004
    Category
    Medical Device
    Distribution
    Distributed nationwide