The Recall Desk

State

North Dakota product recalls

20,324 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.

14501–14525 of 20324

  • ModerateFDA (Drugs)·D-0134-2023·2023-01-25

    Akorn Artificial Tears Eye Drops Recalled for Manufacturing Quality Deviations

    Akorn, Inc. is voluntarily recalling 967,075 bottles of Artificial Tears Solution eye drops nationwide due to manufacturing process deviations identified during quality inspections.

    Product
    Artificial Tears Solution, Lubricant Eye Drops, Polyvinyl Alcohol 1.4%, 15 mL (0.5 fl. oz.) per bottle, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-060-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0163-2023·2023-01-25

    Hand Sanitizer Recalled for Manufacturing Practice Deviations

    Fisher Scientific voluntarily recalls HSANI500ML hand sanitizer (75% isopropyl alcohol) due to manufacturing practice deviations. The product was made under expired temporary FDA approval.

    Product
    Hand Sanitizer, HSANI500ML, (Isopropyl Alcohol), 75% v/v, packaged in a) 500 mL bottle and b) 6 x 500 mL bottles per case, Thermo Fisher Scientific: Janssen Pharmaceuticalaan 3a, 2440 Geel - Belgium, 1 Reagent Lane, Fair Lawn, NJ 07410.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0162-2023·2023-01-25

    Levofloxacin Tablets Recalled for Embossing and Packaging Insert Mismatch

    Macleods Pharma USA recalls Levofloxacin Tablets 500 mg due to mismatched embossing on tablets versus the package insert labeling. The distributed bottles do not match the documented tablet markings.

    Product
    Levofloxacin Tablets, USP 500 mg; 50-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540; Manufactured by: Macleods Pharmaceuticals Ltd., Baddi, Himachal Pradesh, India. NDC 33342-022-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0149-2023·2023-01-25

    Olopatadine HCl ophthalmic solution recalled for manufacturing deviations

    Olopatadine HCl Ophthalmic Solution 0.2% manufactured by Akorn, Inc. is being recalled nationwide due to Current Good Manufacturing Practice (CGMP) deviations affecting 173,928 bottles.

    Product
    Olopatadine HCl Ophthalmic Solution, USP 0.2%, 2.5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-305-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0136-2023·2023-01-25

    Ciprofloxacin ophthalmic solution recalled for manufacturing practice deviations

    Akorn, Inc. is recalling 1,584 bottles of Ciprofloxacin Ophthalmic Solution nationwide due to Current Good Manufacturing Practice (CGMP) deviations. This is a voluntary recall.

    Product
    Ciprofloxacin Ophthalmic Solution, USP 0.3% (Ciprofloxacin HCl), 2.5mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-714-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0150-2023·2023-01-25

    Antihistamine eye drops recalled due to manufacturing process deviations

    Akorn, Inc. is recalling 163,996 bottles of Olopatadine HCl Ophthalmic Solution 0.1% due to manufacturing process deviations. Affected lot numbers expire from October through December 2023.

    Product
    Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL (0.17 FL OZ) per bottle, Antihistamine and Redness Reliever, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC: 51407-499-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0167-2023·2023-01-25

    SINUVA Sinus Implant Recalled for Failed Drug Release Specification

    Intersect ENT, Inc. is recalling 9,898 pouches of SINUVA sinus implants nationwide after detecting failed drug release specifications during stability testing. The implant may not deliver the medication as intended.

    Product
    SINUVA — SINUVA (MOMETASONE FUROATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0138-2023·2023-01-25

    Drug Recall: Erythromycin Ophthalmic Ointment Due to Manufacturing Deviations

    Akorn, Inc. recalls 1.1 million tubes of Erythromycin Ophthalmic Ointment nationwide due to manufacturing deviations. The voluntary, Class II recall was initiated by the firm.

    Product
    ERYTHROMYCIN OPHTHALMIC OINTMENT USP 0.5%, Net Weight: 3.5g (1/8 oz) per tube, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-070-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0146-2023·2023-01-25

    Ofloxacin Ophthalmic Solution Recalled Nationwide for Manufacturing Quality Issues

    Akorn, Inc. is recalling Ofloxacin Ophthalmic Solution 0.3% due to manufacturing quality deviations. The recall affects 65,006 bottles distributed nationwide.

    Product
    Ofloxacin Ophthalmic Solution, USP 0.3%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045; Distributed by: MWI, Boise, ID 83705. NDC: 13985-602-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0160-2023·2023-01-25

    Triamterene and Hydrochlorothiazide Capsules Recalled for Failed Quality Specifications

    Lannett Company is recalling Triamterene and Hydrochlorothiazide Capsules nationwide because certain lots failed impurity and degradation quality specifications. Consumers taking affected lots should consult their pharmacist or physician.

    Product
    Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, 1000 Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 0527-1632-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·23098·2023-01-19

    Sakar International Recalls Three Helmet Models Due to Head Injury Risk

    Sakar International is recalling about 33,100 Credhedz Lizard, Crayola Dry-Erase, and Tony Hawk multi-purpose helmets because they do not meet federal safety standards for positional stability and retention, posing a risk of head injury in a crash.

    Product
    Credhedz Lizard Helmets, Crayola Dry Erase Helmets and Tony Hawk Multi-Purpose Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23093·2023-01-19

    Vanessa 42-inch Fire Tables Recalled for Fire Hazard

    Ove Decors' Vanessa 42-inch fire tables are recalled because the gas hose can melt when contacting the heat shield, causing the table to catch fire. About 470 units sold online from April 2020 through October 2022.

    Product
    Vanessa 42-inch Fire Tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23095·2023-01-19

    Vaenait Baby Children's Robes Recalled for Flammability Hazard

    Vaenait Baby children's robes fail federal flammability standards for sleepwear, posing a burn injury risk. About 2,400 robes sold nationwide between December 2019 and June 2022 are affected.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23103·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    NewCosplay long-sleeved children's sleepwear fails to meet federal flammability standards and poses a burn hazard. The recalled garments were sold exclusively on Amazon from October 2021 through May 2022.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23101·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    Hainan Chong Yu Industrial's NewCosplay children's sleepwear fails federal flammability standards and poses a burn injury risk. About 2,360 units sold on Amazon from October 2021 through May 2022 are affected.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23104·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    About 2,140 units of NewCosplay children's sleepwear fail to meet federal flammability standards and pose a burn injury risk. The recalled garments were sold on Amazon from October 2021 through May 2022.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23105·2023-01-19

    Meguiar's Heavy Duty Headlight Sealant recalled for non-compliant packaging

    Meguiar's is recalling about 140,000 units of Heavy Duty Headlight Sealant because the packaging does not meet federal child-resistant requirements. Young children could be poisoned if they swallow the contents.

    Product
    Heavy Duty Headlight Sealant
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23096·2023-01-19

    Lifetime Brands Recalls Hot Chocolate Pots Due to Fire Hazard

    Lifetime Brands has recalled about 2,700 hot chocolate pots sold at Williams-Sonoma because they are mislabeled as microwave safe. If microwaved, the metallic paint can spark and cause a fire.

    Product
    Hot Chocolate Pots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23094·2023-01-19

    Taylor and Finch Six-Wick Scented Candles Recalled for Fire and Injury Hazards

    Ross Stores is recalling about 5,800 Taylor and Finch six-wick scented candles because they can combust while lit, causing the glass container to break and posing fire and injury hazards. Ross has received five reports of combustion, including one report of minor injury.

    Product
    Taylor and Finch six-wick scented candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23099·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Violation

    NewCosplay branded children's sleepwear fails to meet federal flammability standards, posing a burn risk. About 780 units sold on Amazon from November 2021 through May 2022 are subject to recall.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23100·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Violation

    Weihai Juanhai Decoration Material's NewCosplay children's sleepwear fails to meet federal flammability standards, posing a burn risk. About 280 units were sold on Amazon between December 2021 and May 2022.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23097·2023-01-19

    Children's Pajama Sets Recalled for Flammability Standards Violation

    Selfie Craft Company children's pajama sets fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 38,740 units sold online and in boutiques from November 2017 through June 2022 are affected.

    Product
    Children's Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0884-2023·2023-01-18

    Philips Garbin Ventilator Foam May Separate, Blocking Air Intake

    Silicone foam in some Philips Garbin Ventilators may separate and block the air inlet, reducing therapy volume and causing alarms. Nine units are affected.

    Product
    Philips Garbin Ventilator, Model Number 1058180B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0908-2023·2023-01-18

    Philips Fetal Spiral Electrode may break off during labor monitoring

    Philips is recalling fetal spiral electrodes used for labor monitoring because the spiral tip can break off during use, requiring surgery to remove the fragment from the newborn.

    Product
    Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during labor. PN: 989803137631
    Category
    Medical Device
    Distribution
    Distributed nationwide