The Recall Desk

State

Delaware product recalls

73,187 recalls have nationwide distribution and so reach Delaware. 3,438 additional recalls listed Delaware specifically in their distribution scope.

What the numbers show

Total
3,438
Critical
477
Severe
939
Most recent
2026-09-23

Of the 3,438 recalls naming Delaware we have scored against our rubric, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 939 (27%) are Severe.

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13726–13750 of 76625

  • ModerateFDA (Drugs)·D-0162-2024·2024-01-03

    Albuterol sulfate inhalation aerosol recalled for temperature storage deviation

    Cardinal Healthcare recalls albuterol sulfate inhalation aerosol batch MY7E nationwide due to exposure to temperatures outside labeled storage conditions. The precautionary recall affects 2 cartons.

    Product
    ALBUTEROL SULFATE — ALBUTEROL SULFATE (ALBUTEROL SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0174-2024·2024-01-03

    Colgate Total SF Toothpaste recalled for improper storage temperature exposure

    Colgate Total SF Toothpaste (Batch 1293US561C, 4.8 oz, Clean Mint) distributed nationwide is being recalled due to CGMP deviations where products were exposed to temperatures outside labeled storage conditions.

    Product
    Colgate Total SF Toothpaste, Net Wt 4.8 oz (136 g), Stannous Fluoride 0.454%, Clean Mint, Dist. by: COLGATE-PALMOLIVE CO., New York, NY 10022 USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0185-2024·2024-01-03

    FDA Recalls Jardiance Diabetes Tablets Due to Storage Temperature Deviations

    Jardiance 25 mg tablets distributed nationwide were recalled due to CGMP deviations where products were exposed to temperatures outside the labeled storage conditions. The recall affects batch D41919.

    Product
    JARDIANCE — JARDIANCE (EMPAGLIFLOZIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·065-2023·2023-12-31

    Valley Meats Recalls Ground Beef Products Due to E. Coli O157:H7 Contamination

    Valley Meats LLC is recalling approximately 6,768 pounds of raw ground beef products produced on December 22, 2023, due to possible E. coli O157:H7 contamination.

    Product
    Valley Meats LLC — Valley Meats, LLC, Recalls Ground Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V903000·2023-12-29

    2023–2024 INEOS Grenadier vehicles recalled for faulty steering fasteners

    Ineos Automotive Americas is recalling certain 2023–2024 Grenadier vehicles due to non-locking nuts that may have been installed on the steering rod ball joint, risking steering failure and loss of vehicle control.

    Product
    INEOS — INEOS GRENADIER QUARTERMASTER, GRENADIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24071·2023-12-28

    High-Powered Magnetic Balls Recalled Due to Ingestion Hazard

    A set of 5mm magnetic balls sold online through Walmart.com via Joybuy is being recalled because the magnets are too strong and can cause serious internal injuries or death if swallowed, especially by children.

    Product
    Relax 5mm Science Kit, Large Hematite Magnets Magnetic Stones Building Blocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24070·2023-12-28

    Simpson Gas Pressure Washers Recalled for Lithium Battery Burn Hazard

    FNA Group is recalling about 2,930 Simpson Gas Pressure Washers with Electric Start because the lithium battery in the electric start system can overheat and pose a burn hazard. Two reports of battery overheating have been received, but no injuries have been reported.

    Product
    Simpson Gas Pressure Washers with Electric Start
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0513-2024·2023-12-27

    FDA Recalls Sterile Water and Saline Bottles for Sterility Assurance Issues

    Nurse Assist, LLC is recalling sterile water and saline bottles across multiple brands due to potential lack of sterility assurance. The products could be nonsterile and may cause infection.

    Product
    Sterile Water/Saline: Brand Name: Product Name/Product Code: CARDINAL: 100ML STERILE SALINE BOTTLE/1020, 100ML STERILE SALINE BOTTLE/1022, 100ML STERILE WATER BOTTLE/1024, 100ML STERILE WATER BOTTLE/10000, 100ML STERILE WATER BOTTLE/PT00103419, 100ML STERILE SALINE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0673-2024·2023-12-27

    Fruit Tray Recalled Due to Potential Salmonella Contamination

    TGD Cuts, LLC is recalling a packaged fruit tray due to potential Salmonella contamination. Affected products were distributed in PA, NJ, MD, WV, SC, VA, DE, NC, and NY.

    Product
    FRUIT TRAY 3/64 oz. Packaged in a tray. UPC: 840219166315
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-0622-2024·2023-12-27

    Frozen Salmon Burgers Recalled for Undeclared Sesame and Milk

    Raw Seafoods Inc. is recalling frozen, lightly seasoned salmon burgers nationwide due to undeclared sesame seeds and milk, which pose serious allergic reaction risk to sensitive consumers.

    Product
    Frozen, Lightly Seasoned Salmon Burgers, 28x6oz., 10.5 lbs cases
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0677-2024·2023-12-27

    Melon Tri Color Chunks Recalled for Potential Salmonella Contamination

    TGD Cuts, LLC is recalling Melon Tri Color Chunks due to potential Salmonella contamination. The product was distributed across eight eastern states.

    Product
    MELON TRI COLOR CHUNKS 6/9 OZ Packaged in clamshell containers. UPC:840219192703
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-0537-2024·2023-12-27

    AirFit F20 Full Face Mask recalled for magnetic interference with medical implants

    ResMed is recalling AirFit F20 Full Face Masks due to magnets that can interfere with active medical implants. Updated warnings will guide safe distances for patients and those in close contact.

    Product
    AirFit F20 Full Face Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0681-2024·2023-12-27

    Mixed Fruit Burst Recalled for Potential Salmonella Contamination

    TGD Cuts, LLC is recalling Mixed Fruit Burst 6/10 oz packages due to potential Salmonella contamination. The recall affects products distributed across eight states with use-by dates from November 2–24, 2023.

    Product
    MIXED FRUIT BURST 6/10 OZ Packaged in clamshell containers. UPC: 840219168357
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·23V902000·2023-12-27

    2023-2024 Battle Motors LET2 trucks recalled for steering linkage failure

    Battle Motors is recalling certain 2023 and 2024 LET2 trucks because the drag link in the steering system may become deformed or break, potentially causing complete loss of steering control.

    Product
    BATTLE MOTORS — BATTLE MOTORS LET2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0540-2024·2023-12-27

    AirTouch N20 Nasal Mask recalled for magnetic interference with medical implants

    ResMed is recalling 424,309 units of AirTouch N20 Nasal Masks because they contain magnets that may interfere with active medical implants and ferromagnetic materials. Updated safety warnings are being provided.

    Product
    AirTouch N20 Nasal Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0514-2024·2023-12-27

    Sterile Water and Saline Products Recalled for Lack of Sterility Assurance

    Nurse Assist is recalling sterile water and saline irrigation products due to lack of sterility assurance. Use of nonsterile products could result in infection.

    Product
    Sterile Water/Saline: Product Name/Product Code: CUP STERILE WATER¿ FOIL LID 120 ML/T167005; CUP STERILE SALINE FOIL LID 120 ML/T167007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0684-2024·2023-12-27

    Mixed Fruit Medley Recalled for Potential Salmonella Contamination

    TGD Cuts, LLC is recalling Mixed Fruit Medley products due to potential Salmonella contamination. The recall affects clamshell packages distributed across eight states.

    Product
    MIXED FRUIT MEDLEY 6/6 OZ, 4/16OZ. Packaged in clamshell containers. UPCs: 840219182445 and 840219124292
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0674-2024·2023-12-27

    Cantaloupe chunks and spears recalled for potential Salmonella contamination

    TGD Cuts, LLC is recalling cantaloupe chunks and spears due to potential Salmonella contamination. The products were distributed in Pennsylvania, New Jersey, Maryland, West Virginia, South Carolina, Virginia, Delaware, North Carolina, and New York.

    Product
    Cantaloupe Chunks/Spears: Cantaloupe Chunks 1" 50/2 oz. Packaged in film UPC: 840219184845 Cantaloupe Chunks 1" 2/5 lb. Packaged in trays. UPC: 840219184449 Cantaloupe Chunks 6/16oz. Packaged in clamshell containers. UPC: 840219150345 Cantaloupe Chunks 50/2 oz. Packaged in…
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-0536-2024·2023-12-27

    ResMed AirFit N10 Nasal Masks Recalled for Magnetic Interference with Medical Implants

    ResMed is recalling AirFit N10 Nasal Masks because magnets in the masks may interfere with active medical implants. Patients with such implants should consult their healthcare provider before using these masks.

    Product
    AirFit N10 Nasal Masks and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0153-2024·2023-12-27

    FDA Recalls Phenytoin Oral Suspension Due to Content Uniformity Failure

    The FDA recalled Phenytoin Oral Suspension from Major Pharmaceuticals due to failed content uniformity specifications affecting 3,718 units distributed nationwide.

    Product
    Phenytoin Oral Suspension, USP, 100 mg/4 mL, packaged in packaged in 4 mL unit dose cups (NDC 0904-7079-24), 50 per case (NDC 0904-7079-57), Rx only, Major Pharmaceuticals Livonia, MI 48152
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0541-2024·2023-12-27

    AirFit F30 Full Face Mask recalled for magnetic interference with medical implants

    ResMed is recalling the AirFit F30 Full Face Mask because the device contains magnets that can interfere with active medical implants and ferromagnetic objects. The original user guide did not adequately warn about safe distance requirements.

    Product
    AirFit F30 Full Face Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0151-2024·2023-12-27

    TING 2% Miconazole Nitrate Spray Recalled for Benzene Contamination

    Insight Pharmaceuticals recalls TING 2% Miconazole Nitrate Athlete's Foot Spray due to benzene contamination. The recall affects 117,336 cans distributed nationwide and in Puerto Rico.

    Product
    TING 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder, NET WT 4.5 oz (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591, UPC 363736532611.
    Category
    Drug
    Distribution
    Distributed nationwide