The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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23126–23150 of 26062

  • SevereFDA (Food)·F-0448-2022·2022-01-19

    NutraCap Labs Collares Feliz Capsules Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Hot Pink Collares Feliz Caps Capsules due to undeclared milk. The product was distributed across 25 states and may pose a risk to consumers with milk allergies.

    Product
    Hot Pink Collares Feliz Caps Capsules 30ct Bottle UPC CODE 7 28614 77856 5
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Drugs)·D-0370-2022·2022-01-19

    Methylprednisolone Acetate Injectable Suspension Lacks Sterility Assurance

    Teva Pharmaceuticals is recalling Methylprednisolone Acetate Injectable Suspension 400 mg/10mL due to lack of assurance of sterility. The recall affects one lot distributed to facilities in Tennessee, Mississippi, and Ohio.

    Product
    MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 16714-090-01, packaged in cartons.
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Food)·F-0454-2022·2022-01-19

    Liquid Luck Liquid Lucky Fruit Punch Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Liquid Luck Liquid Lucky Fruit Punch because the product contains undeclared milk, which poses a risk to consumers with milk allergies.

    Product
    Liquid Luck Liquid Lucky Fruit Punch Fruit Punch Sample NO UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0407-2022·2022-01-19

    Alpha Woman Original Capsules recalled for undeclared milk

    NutraCap Labs LLC is recalling Alpha Woman Original Capsules (60ct Bottle, UPC 11883 60220) because the product contains undeclared milk, a common allergen that poses a risk to consumers with milk allergies.

    Product
    Alpha Woman Original Capsules, 60ct Bottle, UPC CODE 11883 60220
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0428-2022·2022-01-19

    NutraCap Labs DL NutriZone Brain Waves Capsules Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling DL NutriZone Genone Brain Waves Capsules (120ct bottles) because the product contains undeclared milk, a common allergen. The recall affects approximately 80,169 units distributed across 26 states.

    Product
    DL NutriZone Genone Brain Waves Capsules 120ct Bottle UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0492-2022·2022-01-19

    Tailor Made Compounding Clarity Capsules recalled for undeclared milk

    NutraCap Labs LLC is recalling Tailor Made Compounding Clarity Capsule 90ct bottles due to undeclared milk. The product was distributed across 25 states.

    Product
    Tailor Made Compounding Clarity Capsule 90ct Bottle NO UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0384-2022·2022-01-19

    Dream Pops Vanilla Sky Bites Recalled for Undeclared Milk Allergen

    Dream Pops 100% Plant-Based Vanilla Sky Bites are being recalled because they contain undeclared milk, a common allergen that may pose a health risk to consumers with milk allergies.

    Product
    100% Plant-Based Dream Pops Vanilla Sky Bites UPC 854097008254
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0430-2022·2022-01-19

    Dube Ortho & PT capsules recalled for undeclared shellfish

    NutraCap Labs LLC is recalling Dube Ortho & PT 144 capsules due to undeclared shellfish in the product. The recall affects 80,169 bottles distributed across 25 states.

    Product
    Dube Ortho & PT 144 Bottles Capsules 60ct No UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0420-2022·2022-01-19

    BlakeFit Everyday Gold Raspberry Lemonade Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling BlakeFit Everyday Gold Raspberry Lemonade Sample due to undeclared milk. The product was distributed across 25 states and poses a risk to consumers with milk allergies.

    Product
    BlakeFit Everyday Gold Raspberry Lemonade Sample NO BARCODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0401-2022·2022-01-19

    Vital Force PUREISO Whey Protein Isolate recalled for undeclared milk

    NutraCap Labs LLC is recalling Vital Force PUREISO 100% Whey Protein Isolate in Creamy Peanut Butter Vanilla flavor because the product contains undeclared milk, a common allergen.

    Product
    Vital Force PUREISO 100% WHEY PROTEIN ISOLATE CREAMY PEANUT BUTTER VANILLA NET WEIGHT: 1122 (1122.0 (39.58 OZ) Ingredients: Whey Protein Isolate, Coconut***StevioBliss Manufactured For Vital Force Rx 1580 Montgomery Hwy #14 Hoover, AL 35216 UPC 8 60006 41005 6
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0432-2022·2022-01-19

    Edel's Collagen Coconut Product Recall for Undeclared Shellfish

    NutraCap Labs LLC is recalling Edel's LLC Edel Beauty Collagen Coconut 25oz jars because they contain undeclared shellfish. The product was distributed across 25 states.

    Product
    Edel's LLC Edel Beauty Collagen Coconut 25oz jar UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0402-2022·2022-01-19

    Vital Force PUREISO Whey Protein Isolate Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Vital Force PUREISO 100% Whey Protein Isolate in Milk Chocolate Cocoa flavor because the product contains undeclared milk, a common allergen. The recall affects Lot No. 2108191 (Exp. 09/2023) distributed across 25 states.

    Product
    Vital Force PUREISO 100% WHEY PROTEIN ISOLATE MILK CHOCOLATE COCOA NET WEIGHT: 1161 (1122.0 (40.95 OZ) Ingredients: Whey Protein Isolate, Coconut***StevioBliss Manufactured For Vital Force Rx 1580 Montgomery Hwy #14 Hoover, AL 35216 UPC 8 60006 41006 3
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0465-2022·2022-01-19

    Subdermal Needle Electrode Corkscrew Recall: Risk of Blue Hub Detachment

    Technomed Europe is recalling 117,672 disposable subdermal needle electrodes due to risk of the blue hub detaching, potentially leaving the needle in the patient's scalp.

    Product
    Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0475-2022·2022-01-19

    First Finisher/Ouro Vitae Mito Male Cherry Limeade contains undeclared milk

    NutraCap Labs LLC is recalling First Finisher/Ouro Vitae Mito Male Cherry Limeade 16oz jars because they contain undeclared milk, a common allergen.

    Product
    First Finisher/Ouro Vitae Mito Male Cherry Limeade 16oz Jar NO UPC CODE
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0488-2022·2022-01-19

    Orthopaedic Stem Implants Recalled for Undersized Bore Manufacturing Defect

    DePuy Orthopaedics is recalling approximately 870 GLOBAL UNITE STD STEM implants worldwide because an undersized spigot bore may prevent proper separation, causing potential surgical delay or bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0458-2022·2022-01-19

    Live Sympl WAKE Blueberry Lemonade Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Live Sympl WAKE Blueberry Lemonade products due to undeclared milk. The recall affects 80,169 units distributed across 25 states.

    Product
    Live Sympl WAKE Blueberry Lemonade Blueberry Lemonade 19oz Jar & Sample pouches UPC CODE 7 28614 78355 2
    Category
    Food
    Distribution
    26 states
  • HighFDA (Food)·F-0500-2022·2022-01-19

    Wycked Naturals Pre OG2 Tiger's Blood recalled for undeclared milk

    NutraCap Labs LLC is recalling Wycked Naturals Pre OG2 Tiger's Blood 25oz Jar (Lot #2009186, exp. 09/2022) because it contains undeclared milk, a common allergen that poses a risk to consumers with milk allergies.

    Product
    Wycked Naturals Pre OG2 Tiger's Blood 25oz Jar UPC CODE 0 51497 12954 5
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0473-2022·2022-01-19

    CT Scanner Software Defect May Degrade Image Quality

    Software version VB20_SP5 in certain Siemens CT scanners may degrade head image quality, increasing misdiagnosis risk. The recall affects 794 units distributed nationwide.

    Product
    SOMATOM Definition AS-Computed tomography system Model 8098027
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0390-2022·2022-01-19

    Local Fixe LLC Frozen Dinner Rolls Wheat Allergen Not Declared

    Local Fixe LLC is recalling frozen dinner rolls because wheat is not declared on the label, even though flour (which contains wheat) is listed as an ingredient. This poses a serious risk to consumers with wheat allergies.

    Product
    Dinner Rolls are shaped in rounds and sold frozen. Packaged in clear plastic Ziploc style plastic bags. The weight per package s 1.323 lbs/600 grams. The label is read in parts: "***Dinner rolls ***Flour, sourdough starter, water, egg, sugar, salt, grape seed oil, active dry y
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0487-2022·2022-01-19

    Orthopaedic Implant Stems Recalled for Undersized Spigot Bore Defect

    DePuy Orthopaedics is recalling GLOBAL UNITE REV STEM SZ 10 implants because the spigot bore may be undersized, preventing proper separation of components during revision surgery and potentially causing bone damage.

    Product
    GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0394-2022·2022-01-19

    Vemondo Vegan Coconut & Cocoa Dessert Cones Recall for Undeclared Milk

    Lidl US Operations is recalling Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones due to undeclared milk allergen. The product was distributed to retail stores in Maryland, Virginia, and Pennsylvania.

    Product
    Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl ounces (110 mL) cones UPC 4 056489 468646
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0386-2022·2022-01-19

    Dream Pops Birthday Cake Bites Recalled for Undeclared Milk Allergen

    Dream Pops 100% Plant-Based Birthday Cake Bites are being recalled because they contain undeclared milk, a known allergen that poses a risk to people with milk allergies.

    Product
    100% Plant-Based Dream Pops Birthday Cake Bites UPC 854097008339
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0477-2022·2022-01-19

    OCT-Camera Laser Shut-Off Malfunction Poses Patient Safety Risk

    Haag-Streit OCT-Camera devices with automatic laser shut-off malfunction may fail to recognize when the laser is safely switched off, posing a potential safety risk.

    Product
    OCT-Camera 211 01 A1, Running software iOCT-Control 3 v1.4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0366-2022·2022-01-19

    Howling Cow Butter Almond Ice Cream recalled for undeclared allergens

    Howling Cow Butter Almond ice cream sold in North Carolina and South Carolina contains Cookie Dough Ice Cream with undeclared soy and wheat allergens. Consumers with allergies should not consume the product.

    Product
    butter almond HOWLING COW THE ICE CREAM OF NC STATE UNIVERSITY One Pint (473 ml) Ingredients: Milk, Cream, Sugar, Almonds***Stabilizer***Carmel Color and Natural Flavor. Contains milk, almonds Proudly distributed by Hunter Farms High Point, NC 27262 UPC 0 74336 65079 6
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0423-2022·2022-01-19

    Chemix Natabolic Capsules recalled for undeclared milk allergen

    NutraCap Labs LLC is recalling Chemix Natabolic Capsules 240ct bottles due to undeclared milk, which poses a serious risk to consumers with milk allergies. The affected product was distributed across 25 states.

    Product
    Chemix Natabolic Capsules 240ct Bottle UPC CODE 8 60003 22042 9
    Category
    Food
    Distribution
    26 states