The Recall Desk

State

North Dakota product recalls

73,388 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
869
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 869 (30%) are Severe.

Which agencies issued them

These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20651–20675 of 76312

  • SevereFDA (Devices)·Z-1271-2022·2022-06-29

    Medfusion Syringe Pump Recalled Due to Multiple Infusion Control and Alarm Failures

    Smiths Medical recalled 58,671 Medfusion Syringe Pump units worldwide due to multiple failures that could interrupt therapy or cause over-infusion, including defective alarms and display errors.

    Product
    Medfusion Syringe Pump Model: Model 4000-0100-50, Model 4000-0101-249, Model 4000-0101-50, Model 4000-0101-51, Model 4000-0101-78, Model 4000-0105-249, Model 4000-0105-51, Model 4000-0105-78, Model 4000-0106-00, Model 4000-0106-01, Model 4000-0106-231
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1334-2022·2022-06-29

    Albertsons Ready Meals Quad recalled for potential Salmonella contamination

    Albertsons Companies LLC is recalling Ready Meals Quad Peanut Butter Apple Pretzel Brownie products across 32 states due to potential Salmonella contamination. All products with sell-through dates up to May 24, 2022 are affected.

    Product
    Ready Meals Quad Peanut Butter Apple Pretzel Brownie. Product were available for purchase at the following banners: ACME, Albertsons, Andronico's Community Markets, Carrs-Safeway, Eagle, King's, Balducci's, Lucky, Pak 'N Save, Safeway, Vons. Packaged in clear plastic square…
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1332-2022·2022-06-29

    Ready Meals PB & Trail Mix Snack recalled for potential Salmonella contamination

    Albertsons Companies LLC recalled Ready Meals PB & Trail Mix Snack due to potential Salmonella contamination. Products were sold at Shaw's and Star Market locations across 31 states.

    Product
    Ready Meals PB & Trail Mix Snack. Product were available for purchase at the following banners: Shaw's, Star Market. Packaged in clear plastic square bottom and lid. Net wt. 7.6 oz.
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1321-2022·2022-06-29

    Chocolate Peanut Butter Cups Recalled for Salmonella Contamination

    Albanese Confectionery Group recalls Rich's Milk Chocolate peanut butter cups nationwide due to Salmonella contamination from recalled Jif peanut butter used in manufacturing.

    Product
    Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Rich s Milk Chocolate Mini Peanut Butter Cups; 2ct 5lb bulk per 10 lb case. Product not retail packaged, distributed for bulk sale at retail.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1337-2022·2022-06-29

    Chocolate fudge with peanut butter recalled for potential Salmonella

    Calico Cottage Inc is recalling chocolate fudge products containing peanut butter due to potential Salmonella contamination. The recall affects 677 units distributed nationwide.

    Product
    1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not consumer packaging, bulk carton 2. PEANUT BUTTER CHOC FUDGE LAYERED (6S) 6LB NET WT - not consumer packaging, bulk carton 3. PEANUT BUTTER CHOCOLATE FUDGE (6SS) 6LB NET WT - not consumer packaging, bulk carton
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1272-2022·2022-06-29

    Medfusion Syringe Pump Class I Recall: Risk of Over-Infusion or Therapy Interruption

    Smiths Medical is recalling multiple Medfusion Syringe Pump models due to software and hardware defects that may interrupt drug infusion or cause over-infusion. Approximately 65,093 units distributed worldwide are affected.

    Product
    Medfusion Syringe Pump Models: 3500, 3500-0600-00, 3500-0600-01, 3500-0600-249, 3500-0600-50, 3500-0600-51, 3500-0600-82, 3500-306, 3500-402, 3500-414, 3500-415, 3500-500, 3500BC, 3500E, 3500G, 3500SD, 3500SD-500, 3500VX, 3500VX-306, 3500VX-414, 3500VX-415, 3500VX-500, 3500ZE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1330-2022·2022-06-29

    Albertsons Grab & Go Apple & Celery Tray recalled for potential Salmonella

    Albertsons Companies recalled Grab & Go Apple & Celery Tray w/Peanut Butter products due to potential Salmonella contamination. Products with sell-through dates up to May 24, 2022 are affected.

    Product
    Grab & Go Apple & Celery Tray w/Peanut Butter. Product were available for purchase at the following banners: United, Amigos, Market Street, Albertsons Market. Packaged in clear plastic container and lid.
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-1266-2022·2022-06-29

    HeartWare HVAD Battery Model 1650DE May Malfunction Due to Weld Defect

    Medtronic is recalling HeartWare HVAD batteries (Model 1650DE) due to an internal weld defect that can cause battery malfunction and prevent proper charging. Approximately 429 affected batteries were distributed worldwide.

    Product
    HeartWare Battery, Model #1650DE, a component of the HeartWare Ventricular Assist Device (HVAD) System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1331-2022·2022-06-29

    Albertsons Peanut Butter and Chocolate Filled Jumbo Cupcakes Recalled for Salmonella

    Albertsons recalled peanut butter and chocolate filled cupcakes due to potential Salmonella contamination. The recall affects products sold at Safeway, Andronico's, Vons, and Pak 'N Save with sell-through dates up to May 26, 2022.

    Product
    Peanut Butter & Chocolate Filled Jumbo Cupcake. Product were available for purchase at the following banners: Safeway, Andronico's Community Markets, Vons, Pak 'N Save. Packaged in clear plastic bottom and lid. Net wt. 7.92 oz.
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1326-2022·2022-06-29

    Albertsons Apples with Peanut Butter Recalled for Salmonella Risk

    Albertsons Companies is recalling Apples Sliced with Peanut Butter due to potential Salmonella contamination. The product was sold at Albertsons, Safeway, and Lucky stores across 32 states with sell-through dates up to May 24, 2022.

    Product
    Apples Sliced With Peanut Butter. Product were available for purchase at the following banners: Albertsons, Safeway, Lucky. Packaged in clear plastic cup and lid. Net wt. 8 oz.
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1340-2022·2022-06-29

    Salted Nut Roll Fudge Recalled for Potential Salmonella in Peanut Butter

    Calico Cottage Inc is recalling Salted Nut Roll Pre-Made Fudge nationwide because the peanut butter ingredient is potentially contaminated with Salmonella.

    Product
    1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not consumer package, bulk carton
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1325-2022·2022-06-29

    Mini Peanut Butter Cream Pie recalled due to potential Salmonella

    Albertsons Companies LLC is recalling Mini Peanut Butter Cream Pies sold at Haggen stores across 32 states due to potential Salmonella contamination. Consumers should not consume the affected pies.

    Product
    Mini Peanut Butter Cream Pie. Product was available for purchase at the following banner: Haggen. Packaged in clear plastic square bottom and lid.
    Category
    Food
    Distribution
    32 states
  • HighFDA (Devices)·Z-1274-2022·2022-06-29

    Colonovideoscope Model CF-H180AL recalled due to narrowed viewing angle

    Olympus Corporation recalls a single colonovideoscope model CF-H180AL because an incorrect camera unit was installed, causing narrower viewing angle and potential device protrusion that could injure tissue. No injuries have been reported.

    Product
    Colonovideoscope Model CF-H180AL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1156-2022·2022-06-29

    Tretinoin Capsules Recalled Nationwide for Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling Tretinoin Capsules (10 mg) nationwide due to failed dissolution specifications that may affect medication effectiveness. Patients should contact their pharmacist or doctor to confirm if their prescription is affected.

    Product
    Tretinoin Capsules, 10 mg, Rx Only, 100 capsules per bottle, Teva Pharmaceuticals USA Inc., North Wales, PA, 19454, NDC 0555-0808-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1153-2022·2022-06-29

    Testosterone Cypionate Injectable Recalled for Manufacturing Quality Issues

    Sun Pharmaceutical recalls 97,450 vials of Testosterone Cypionate Injection nationwide due to manufacturing deviations that could cause out-of-specification impurities.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1154-2022·2022-06-29

    Testosterone Cypionate Injectable Recalled Due to Manufacturing Sterility Deviation

    Sun Pharmaceutical is recalling approximately 47,500 vials of Testosterone Cypionate Injection due to a manufacturing deviation that may have affected product sterility.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1345-2022·2022-06-29

    Ice cream recall for undeclared tree nut allergen

    Red Button Vintage Creamery Canadian Vanilla Ice Cream was distributed nationwide with undeclared almond allergen due to packaging mix-up. Consumers with tree nut allergies should not consume this product.

    Product
    Red Button Vintage Creamery Canadian Vanilla Ice Cream, 56 ounce tub, UPC 0 77865 01001 7, Distributed by Associated Foods Stores, Salt Lake City, UT, 84119. Store Frozen.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1273-2022·2022-06-29

    FDA Recalls Catheter Drainage Kits With Wrong Needle Size

    Bard Peripheral Vascular Inc is recalling certain catheter drainage kits that may contain an 8 Fr needle instead of the correct 6 Fr needle. The incorrect needle size could cause tissue injury during patient care.

    Product
    REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1347-2022·2022-06-29

    Kava Glycerite Recalled Due to High Yeast and Mold Contamination

    EarthLab Inc is recalling Wise Woman Herbals Standardized Kava Glycerite due to high yeast and mold counts detected during microbial testing. The affected product was distributed nationwide.

    Product
    Wise Woman Herbals Standardized Kava Glycerite, product is liquid and contains 15 mg Kavalactones (from Piper methysticum) and 9 mg Kavalactones (from Piper methysticum) depending on lot. Dosage: 60 drops 1-2 times a day. Product is packaged in Amber Glass Boston Round…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1151-2022·2022-06-29

    Isopropyl Alcohol bottles recalled for defective containers and leakage

    Vi-Jon's 70% isopropyl alcohol bottles may leak when squeezed or tilted due to defects in the bottle neck finish. Over 3 million bottles with various lot numbers were distributed nationwide.

    Product
    ISOPROPYL ALCOHOL — ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1155-2022·2022-06-29

    Clonazepam Tablets Recalled Due to Manufacturing Defect

    Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets (0.125mg) due to manufacturing defects where oversized tablets were found. The affected lot (MHC1430A, exp. 09/2023) was distributed nationwide.

    Product
    Clonazepam Orally Disintegrating Tablets, USP, 0.125mg, Rx Only, 60 Tablets, Mfd. by: Sun Pharmaceutical Industries Ltd. Mumbai, India, Dist. by: Sun Pharmaceutical Industries In., Cranbury, NJ 08512, NDC 57664-783-68, packaged in bottles.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1281-2022·2022-06-29

    BVI Wet-Field Eraser surgical devices shipped with incorrect tip configuration

    Beaver Visitec International recalled 660 units of BVI Wet-Field Eraser surgical devices after discovering boxes labeled with one tip configuration contained a different tip design. This mismatch could affect surgical precision and hemostasis control.

    Product
    BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high frequency electrical current Part Number: 221251
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1282-2022·2022-06-29

    INTERGARD Woven Vascular Graft mislabeled with incorrect size specification

    Maquet Cardiovascular recalls INTERGARD Woven Vascular Grafts with incorrect labeling. Units labeled as 8 mm diameter instead contained 32 mm diameter grafts.

    Product
    INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2022·2022-06-29

    Cardiac device software recalled for inadequate electrical insulation

    CardioTek EP-TRACER Software V2.x is recalled because it failed electrical safety testing for insulation. The 146 affected units were distributed worldwide.

    Product
    CardioTek EP-TRACER Software V2.x.
    Category
    Medical Device
    Distribution
    Distributed nationwide