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.

15526–15550 of 20364

  • ModerateFDA (Devices)·Z-1770-2022·2022-09-28

    Dialysis water-treatment unit recalled for missing ferrite cores in cables

    Fresenius is recalling 6 units of the AquaC UNO H reverse osmosis unit used with hemodialysis systems due to missing ferrite cores in internal ethernet cables affecting electromagnetic compatibility.

    Product
    AquaC UNO H [120V, 60Hz, 1700VA, US-Version- a reverse osmosis unit intended for use with hemodialysis systems. Fresenius Part Number: 24-0970-1 Vivonic Part Number: G02000966-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1738-2022·2022-09-28

    Mountain Dew Major Melon Zero 12-pack cans have incorrect sugar-content labeling

    Mountain Dew Major Melon Zero 12-pack cans sold nationwide are labeled 'Full Sugar' on the can despite containing Zero Sugar formula. The actual product is correct; only the can label is mislabeled.

    Product
    Mountain Dew Major Melon Zero, 12 FL OZ (355mL) can, sold as 12 pack. Bottled under the authority of Pepsico, Inc. Purchase, NY 10577. UPC 0 12000 20506 4 (can) UPC 0 12000 20507 1 (12 pack carton)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1771-2022·2022-09-28

    Diversatek M-Catch Retrieval Nets: incorrect inner polybag labeling

    Diversatek Healthcare is recalling M-Catch Retrieval Nets (Part Number REF 1175-01, Lot Number 001919) due to incorrect inner polybag labeling. 245 devices were distributed nationwide between September and October 2021.

    Product
    Diversatek Health, M-Catch Retrieval Nets, Part Number REF 1175-01, Quantity 5 EA/u. Used to endoscopically retrieve severed polyps, tissue samples, food bolus, and foreign bodies in the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1541-2022·2022-09-28

    Clonidine Hydrochloride 0.3 mg Tablets Recalled for Strength Mix-up

    UNICHEM PHARMACEUTICALS is recalling Clonidine Hydrochloride Tablets labeled 0.3 mg that contain 0.2 mg tablets instead. The recall affects 18,960 bottles (Lot # GCLH22005) distributed nationwide.

    Product
    CLONIDINE HYDROCHLORIDE — CLONIDINE HYDROCHLORIDE (CLONIDINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1774-2022·2022-09-28

    Fungitell STAT IVD Assay affected by incorrect printed reconstitution instructions

    Associates of Cape Cod is recalling Fungitell STAT IVD Assay kits due to incorrect printed information on clamshells regarding reconstitution and pretreatment volumes. Users should verify procedures against official documentation before use.

    Product
    Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Ref: FT007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·22227·2022-09-22

    Spalding Momentous EZ Portable Basketball Goals Recalled for Impact Injury Risk

    Russell Brands is recalling about 13,400 Spalding Momentous EZ Portable Basketball Goals because welds in the arm attaching the backboard to the pole can fail, causing the backboard to fall and strike users. The firm has received 26 reports of weld failures and 2 injury reports.

    Product
    Spalding Momentous EZ Portable Basketball Goals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22776·2022-09-22

    Pool and Spa Drain Covers Recalled for Entrapment Hazard

    Angzhili pool and spa drain covers do not meet the Virginia Graeme Baker Pool and Spa Safety Act entrapment protection standards, posing a risk to swimmers and bathers. About 1,000 units sold on Amazon from June 2021 through June 2022 are affected.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22774·2022-09-22

    Wadoy pool and spa drain covers recalled for entrapment hazard

    Find4Fix has recalled about 5,500 Wadoy eight-inch pool and spa drain covers sold on Amazon from August 2019 through June 2022 because they do not meet Virginia Graeme Baker Pool and Spa Safety Act entrapment protection standards.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22773·2022-09-22

    Pool and Spa Drain Covers Recalled for Entrapment Hazard

    Chyir Myd pool and spa drain covers do not meet federal entrapment-protection standards and pose a hazard to swimmers. About 300 units were sold on Amazon from September 2021 through June 2022.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22777·2022-09-22

    Canyon Furniture Ladders Recalled for Entrapment and Strangulation Hazards

    Canyon Furniture Company is recalling approximately 2,100 ladders sold with Canyon Lake and Cottage Colors bunk bed and hutch sets due to a gap wider than 3.5 inches between the fourth ladder step and the hutch cross-member that poses entrapment and strangulation hazards. No injuries have been reported.

    Product
    Ladders sold with Canyon Lake and Cottage Colors Bunk Bed and Hutch Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22775·2022-09-22

    Pool and Spa Drain Covers Recalled for Entrapment Hazard

    Goetas pool and spa drain covers do not meet the Virginia Graeme Baker Pool and Spa Safety Act standards, creating an entrapment hazard for swimmers and bathers. About 300 units were sold on Amazon from October 2021 through April 2022.

    Product
    Pool and spa drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22226·2022-09-22

    Miffy First LED Lights Recalled for Overheat Burn Hazard

    About 1,400 Miffy First LED Lights can overheat during use, posing a burn hazard. No injuries have been reported. Consumers should stop using the lights and contact the company for a free module replacement.

    Product
    Miffy First LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22228·2022-09-22

    Accompany USA Ceramic Mugs with Cork Bottoms Recall Due to Burn Hazard

    Accompany USA is recalling about 25,000 ceramic mugs with cork bottoms because they can crack or break when hot liquid is poured into them, posing a burn hazard. One incident of breakage has been reported with no injuries.

    Product
    Ceramic Mugs with Cork Bottoms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1509-2022·2022-09-21

    Walgreens Dye-Free Magnesium Citrate Laxative Recalled for Microbial Contamination

    Vi-Jon, LLC is recalling Walgreens Dye-Free Magnesium Citrate Saline Laxative due to microbial contamination of the non-sterile product. Approximately 29,172 bottles distributed nationwide in the USA, Canada, and Panama are affected.

    Product
    Walgreens, Dye-Free, Magnesium Citrate, SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Lemon Flavor, 10 FL OZ (296 mL), Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-8166-38 UPC 3 11917 20160 3 (green label)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1540-2022·2022-09-21

    Propofol Injectable Emulsion Recalled for Particulate Matter Contamination

    Pfizer is recalling 5,390 vials of Propofol Injectable Emulsion due to the presence of particulate matter. The affected lot (EA7470, expiration 6/1/2023) was distributed nationwide.

    Product
    PROPOFOL — PROPOFOL (PROPOFOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1504-2022·2022-09-21

    Meijer Magnesium Citrate Laxative Recalled for Microbial Contamination

    Meijer brand magnesium citrate laxative (10 fl oz) has been recalled nationwide due to microbial contamination of Lot 0557622. Consumers should discard or return the product.

    Product
    meijer, magnesium citrate Saline Laxative, Oral Solution, (1.745 g/fl oz), Lemon Flavor, 10 FL OZ (296 mL), Dist. By Meijer Distribution, Inc. Grand Rapids, MI 49544; NDC 41250-708-38 UPC 7 13733 45945 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1500-2022·2022-09-21

    CVS Health Magnesium Citrate Saline Laxative recalled for microbial contamination

    CVS Health Magnesium Citrate Saline Laxative is being recalled due to potential microbial contamination of the non-sterile product. Approximately 241,086 bottles were distributed nationwide.

    Product
    CVS Health, Magnesium Citrate SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Lemon Flavor, 10 FL OZ (296 mL), a) UPC 0 50428 30594 2; b) UPC 0 50428 33517 8; Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1506-2022·2022-09-21

    FDA Recalls Citroma Magnesium Citrate Laxative for Microbial Contamination

    Citroma magnesium citrate laxative is recalled due to microbial contamination. The FDA Class I recall affects 42,912 bottles distributed in the USA, Canada, and Panama.

    Product
    CITROMA — CITROMA (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1507-2022·2022-09-21

    SWAN Citroma Saline Laxative Recalled for Microbial Contamination

    Vi-Jon is recalling SWAN Citroma Magnesium Citrate Saline Laxative (10 FL OZ bottles) due to microbial contamination of a non-sterile product. The product was distributed nationwide in the USA, Canada, and Panama.

    Product
    SWAN, Citroma MAGNESIUM CITRATE, Saline Laxative, Oral Solution, (1.745 g/fl oz), Lemony Flavor, 10 FL OZ (296 mL), Distributed by: Vi-Jon, Inc. One Swan Drive Smyrna, TN 37167; NDC 0869-0166-38 UPC 0 72785 13405 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1653-2022·2022-09-21

    Baxter CLEARLINK System Non-DEHP Solution Set recalled due to leak reports

    Baxter Healthcare Corporation is recalling the CLEARLINK System Non-DEHP Solution Set nationwide due to increased customer reports of leaks in the in-line injection site device.

    Product
    Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection site.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0212-2024·2022-09-21

    Banana Boat Clear Sunscreen Spray recalled for benzene contamination

    Edgewell Personal Care Brands is recalling Banana Boat hair & scalp defense Clear Sunscreen Spray SPF 30 due to benzene contamination. The affected product was distributed nationwide in the United States.

    Product
    Banana Boat hair & scalp defense, Clear Sunscreen Spray SPF 30, Avobenzone 2.0%, Homosalate 6.0%, Octocrylene 6.0%, packaged in Net Wt 6 oz. aluminum spray can, Distributed by: Edgewell Personal Care Brands, LLC, Shelton, CT 06484, UPC 0 79656 04041 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1505-2022·2022-09-21

    Magnesium Citrate Laxative Recalled Due to Microbial Contamination

    Vi-Jon's Magnesium Citrate oral solution laxative is recalled nationwide due to microbial contamination. Approximately 8,682 bottles are affected.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1502-2022·2022-09-21

    FDA Recalls CITROMA Magnesium Citrate for Microbial Contamination

    Vi-Jon, LLC is recalling CITROMA magnesium citrate oral laxative solution due to microbial contamination. The affected product was distributed nationwide in the USA, Canada, and Panama.

    Product
    CITROMA — CITROMA (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1510-2022·2022-09-21

    Walgreens Magnesium Citrate Laxative Recalled for Microbial Contamination

    Walgreens Dye-Free Magnesium Citrate Saline Laxative is recalled nationwide due to microbial contamination affecting certain lots. Consumers should stop using the product immediately.

    Product
    Walgreens, Dye-Free, Magnesium Citrate, SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Grape Flavor, 10 FL OZ (296 mL), Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015; NDC 0363-7162-38 UPC 3 11917 20159 7 (purple label).
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1508-2022·2022-09-21

    OTC Magnesium Citrate Laxative Recalled for Microbial Contamination

    Vi-Jon's CITROMA magnesium citrate laxative is recalled due to microbial contamination. Approximately 18,588 bottles were distributed nationwide in the USA, Canada, and Panama.

    Product
    CITROMA — CITROMA (MAGESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide