The Recall Desk

State

North Dakota product recalls

20,322 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.

14151–14175 of 20322

  • HighFDA (Food)·F-0352-2023·2023-02-22

    Starbucks Vanilla Frappuccino Recalled for Potential Glass Contamination

    PepsiCo is recalling Starbucks Vanilla Frappuccino bottles nationwide due to potential glass contamination. Consumers should not consume affected bottles.

    Product
    Starbucks frappuccino Vanilla. Chilled Coffee Drink. 13.7 Fl Oz (405mL). UPC 0 12000-81331 3. Starbucks Coffee Company. For comments or questions, call 1-800-211-8307.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0321-2023·2023-02-22

    FDA Recalls TPN Nutrition Bags Due to Sterility Assurance Failure

    Sentara Infusion Services recalls 24 bags of TPN (Total Parenteral Nutrition) distributed nationwide due to lack of sterility assurance. The recall affects prescription intravenous nutrition products.

    Product
    TPN (a) 95GM/AA, 385/DEX, 50GM/LIP 1800ML, (b)TPN AA:100GM DEX:250GM LIP:50GM 2400ML, (c) TPN: AA 80GM ; DEX 320GM ; LIP 50GM IN 2300 ml, Rx only, use with Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0302-2023·2023-02-22

    Levothyroxine Injectable Syringes Recalled Due to Lack of Sterility Assurance

    Sentara Infusion Services is recalling levothyroxine injectable syringes dispensed nationwide due to lack of sterility assurance. Patients should contact their healthcare provider if they received this product.

    Product
    LEVOTHYROXINE 25MCG IN NS 1.25ML SYRINGE, Thyroid, Rx Only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0283-2023·2023-02-22

    Ceftriaxone injectable antibiotic recalled for lack of sterility assurance

    Sentara Infusion Services recalled 72 bags of ceftriaxone injectable antibiotic due to lack of sterility assurance. The affected product was distributed nationwide with a beyond-use date of December 24–31, 2022.

    Product
    CEFTRIAXONE (a) 2GM in NS 100ml, (b) 4GM IN NS 200ML, Antibiotic, used with a Curlin or Home pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0286-2023·2023-02-22

    Daptomycin Antibiotic Injectable Syringes Recalled for Lack of Sterility Assurance

    Sentara Infusion Services is recalling Daptomycin pre-filled syringes distributed nationwide due to lack of sterility assurance. Patients using this antibiotic should contact their healthcare provider immediately.

    Product
    DAPTOMYCIN (a)360MG in NS 18ML syringe (b)580MG IN NS 29ML syringe(c) 630MG IN NS 31.5ML used with a home pump; antibiotic, Rx only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0292-2023·2023-02-22

    Ethanol 70% Syringes Recalled Due to Lack of Sterility Assurance

    Sentara Infusion Services is recalling 17 units of ETHANOL 70% 0.5ML syringes distributed nationwide due to lack of sterility assurance. The syringes may not meet required sterility standards for safe injection.

    Product
    ETHANOL 70% 0.5ML SYRINGE, Cathcare, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0310-2023·2023-02-22

    Nafcillin Antibiotic Infusion Recalled Due to Sterility Assurance Failure

    Sentara Infusion Services is recalling 16 bags of nafcillin antibiotic infusion nationwide due to lack of sterility assurance. Patients should contact their healthcare provider immediately.

    Product
    NAFCILLIN 24GM IN NS 1200ML, antibiotic, Rx Only, use with a Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0272-2023·2023-02-22

    FDA Recalls 0.9% Sodium Chloride Solution for Lack of Sterility Assurance

    Sentara Infusion Services is recalling 114 bags of 0.9% Sodium Chloride intravenous solution due to lack of sterility assurance. The product was distributed nationwide with Beyond Use dates of December 24–31, 2022.

    Product
    0.9% Sodium Chloride, used as a diluent or hydration, packaged volume of (a)1000ML (b)2000ML (c) 720ML, used with Curlin pump, no pump or gravity. Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0285-2023·2023-02-22

    Intravenous hydration solution recalled for lack of sterility assurance

    Sentara Infusion Services is recalling D5W1/2NS W/ 77MEQ OF SOD ACETATE 1000ML intravenous hydration solution due to lack of sterility assurance. Eight bags were dispensed to patients nationwide.

    Product
    D5W1/2NS W/ 77MEQ OF SOD ACETATE 1000ML, Hydration, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0291-2023·2023-02-22

    Ertapenem Injectable Antibiotic Bags Recalled for Lack of Sterility Assurance

    Sentara Infusion Services is recalling 22 bags of Ertapenem (Invanz) injectable antibiotic due to lack of sterility assurance. The product was dispensed nationwide to patients receiving home infusion therapy.

    Product
    Ertapenem (Invanz) 1GM NS 100ML, antibiotic, use with home pump, Rx Only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0294-2023·2023-02-22

    Ganciclovir Injectable Solution Recalled Due to Lack of Sterility Assurance

    Sentara Infusion Services is recalling Ganciclovir (Cytovene) injectable solutions due to lack of sterility assurance. The medication was dispensed to patients nationwide.

    Product
    GANCICLOVIR ( CYTOVENE) (a)1480MG IN NS 296ML, (b) 740 MG IN NS 336 ML, antiviral, Rx Only, use with a Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0326-2023·2023-02-22

    FDA Recalls Humatrix Microclysmic Gel for Manufacturing Practice Violations

    Consolidated Chemical, Inc. is recalling 3186 bottles of Humatrix Microclysmic Gel nationwide due to deviations from proper manufacturing practices.

    Product
    Humatrix Microclysmic Gel, 8 oz per bottle, Care-Tech Laboratories, Inc., Saint Louis, Missouri 63139.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1127-2023·2023-02-22

    Surgical Circumcision Kits Recalled Due to Non-Sterile Outer Wrapping

    MEDLINE INDUSTRIES is recalling CENTURION MEDICAL PRODUCTS Circumcision Tray kits (Lot 22HMH649) because the outer packaging is non-sterile, though the surgical contents inside remain sterile.

    Product
    Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS CIRCUMCISION TRAY, Reorder Number CIT3345
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1131-2023·2023-02-22

    HydroPICC Catheters Recalled for Incorrect Expiration Date Labeling

    Access Vascular, Inc is recalling HydroPICC 4Fr Single Lumen catheters (Model 80001001) due to incorrect expiration date labeling. The devices expire earlier than the labeled date.

    Product
    HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0325-2023·2023-02-22

    FDA recalls Techni-Care Chloroxylenol antiseptic due to manufacturing deviations

    Consolidated Chemical is recalling Techni-Care Chloroxylenol 3% in 4 oz and 8 oz bottles nationwide due to manufacturing practice violations. No illnesses have been reported.

    Product
    Techni-Care Chloroxylenold 3%, [4 fl oz /118 mL or 8 fl oz/236 mL] per bottle, Care-Tech Laboratories, Inc., Saint Louis, Missouri 63139. NDC 4 oz bottle: 46706-222-01; NDC 8 oz: 46706-222-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·23126·2023-02-16

    Paradise Grills First Generation Outdoor Kitchens Recalled for Fire and Burn Hazards

    About 18,000 Paradise Grills First Generation Outdoor Kitchens are recalled because liquid propane gas can accumulate in the closed lid and cabinets, causing an explosion and severe burns when the grill is relit. Two reports of explosions causing severe burns have been received.

    Product
    Paradise Grills First Generation Outdoor Kitchens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23127·2023-02-16

    Kids Preferred Disney Character Figurines Recalled for Choking Hazard

    Kids Preferred is recalling soft vinyl Disney character figurines because the arms or legs can detach, posing a choking hazard to children. About 16,140 units were sold nationwide through retailers including BuyBuy Baby and Amazon from May through December 2022.

    Product
    My First Mickey Mouse, Minnie Mouse, Buzz Lightyear, and Stitch Figurines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23123·2023-02-16

    Children's Nightgowns Recalled for Flammability Standard Violation

    Betsy & Lace children's nightgowns fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 90,550 units sold online from March 2018 through September 2022.

    Product
    Children's nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23120·2023-02-16

    Wicked Lights ScanPro Night Hunting Headlamps Recalled for Burn Hazard

    AllPredatorCalls.com is recalling approximately 12,000 Wicked Lights ScanPro night hunting headlamps because a wire short can cause the wire to heat up and melt, posing a burn hazard. The company has received 14 reports of wire heating and melting, including two burn injuries.

    Product
    Wicked Lights ScanPro Night Hunting Headlamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23125·2023-02-16

    KLIM Backcountry Probes A300 Recalled Due to Failure Risk

    KLIM Backcountry Probes A300 can fail to operate when deployed to locate avalanche victims, posing a risk of severe injury or death. Consumers should stop using the product immediately and contact KLIM for a full refund.

    Product
    KLIM Backcountry Probes A300
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23121·2023-02-16

    Children's Nightgowns Recalled for Flammability Standard Violation

    The Oaks Apparel Company is recalling about 320 children's nightgowns that fail to meet federal flammability standards for sleepwear, posing a burn injury risk. Consumers should stop using them immediately.

    Product
    Children's nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23122·2023-02-16

    Hatley USA Children's Pajamas and Headbands Recalled

    Hatley USA is recalling about 7,640 children's pajamas and about 300 headbands. The pajamas fail to meet federal flammability standards and pose a burn hazard; the headbands contain excess lead that is toxic if ingested.

    Product
    Children's pajamas and headbands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23727·2023-02-16

    Linus Bike Recalls Electric Bicycles Due to Crash Hazard

    Linus Bike is recalling about 430 electric bicycles (Cesta 500 and Ero 500 models) because the front fork can crack, posing a crash hazard. No injuries have been reported.

    Product
    Electric bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1056-2023·2023-02-15

    GE Nuclear Medicine Imaging Systems detector fall hazard

    GE Nuclear Medicine 600/800 series imaging systems may have faulty detectors that could fall, causing serious injury. Mitigation measures may not be properly implemented on 34 units distributed worldwide.

    Product
    GE Nuclear Medicine 600/800 series systems, specifically: a) OPTIMA O640 X 3/8 inch NR, b) DISCOVERY O640 X 3/8 inch, c) NM OPTIMA O640 X 3/8 inch, d) O640 NM Gantry 3/8 inch, e) O640 NM GANTRY FINAL ASSY, f) OPTIMA O640 X 3/8 inch; Emission Computed Tomography System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1054-2023·2023-02-15

    GE Nuclear Medicine Systems: Detector Fall Risk Due to Faulty Mitigation

    GE Nuclear Medicine 600/800 series systems (748 units distributed worldwide) may have improperly implemented detector fall mitigations. If the mitigation fails, the detector can fall and cause life-threatening bodily injury.

    Product
    GE Nuclear Medicine 600/800 series systems, specifically: a) 830, b) 830 / Dismount, c) 830 /, d) 830 / 5842894-20, e) 830 / Dismount / 50HZ, f) 830 / Dismount / 60HZ, g) 830 3/8 inch Detector, h) 830 BJ, i) 830 BJ / 5144407, j) 830 BJ / Dismount, k) 830 ES DEM, l) 8
    Category
    Medical Device
    Distribution
    Distributed nationwide