The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mis labeling recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

2501–2525 of 9607

  • HighFDA (Food)·F-0073-2020·2019-10-30

    Trails End Sweet and Savory Collection Recalled for Undeclared Nuts

    Weaver Fundraising is recalling the Trails End Sweet and Savory Collection due to inaccurate nutrition facts and undeclared almonds, cashews, and pecans.

    Product
    Trails End Sweet and Savory Collection, containing White Cheddar cheese Corn (5 oz.), Butter Toffee Carmel Corn (20 oz.), and Chocolatey Caramel Crunch (15 oz.) each in individual foil bags packaged together in variety box
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0059-2020·2019-10-30

    Shirakiku Buckwheat Noodles Recalled for Undeclared Fish Allergens

    Wismettac Asian Foods is recalling Shirakiku Buckwheat Noodles because the dipping sauce contains undeclared tuna and fails to list fish as an allergen.

    Product
    Shirakiku Buckwheat Noodles Yamaimo Soba With Concentration Soup Base, 435G SK, UPC 074410455200 Distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA 90670
    Category
    Food
    Distribution
    17 states
  • HighFDA (Food)·F-0074-2020·2019-10-30

    Koppers Chocolate Gummy Bears Recalled for Missing Milk Allergen Labeling

    The Newark Nut Store is recalling Koppers Chocolate Dark Chocolate Gummy Bears because the packaging fails to list milk as an allergen.

    Product
    Koppers Chocolate Dark Chocolate Gummy Bears, 4oz (113g) retail package, metallized foil resealable pouch, 12 pouches per case
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0054-2020·2019-10-30

    Tia Rita's Cornbread Mix Recalled for Undeclared Wheat Allergen

    The Truck Farm, LLC is recalling Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix because the product contains wheat flour but does not declare wheat on the label.

    Product
    Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix. Packaged in 13 oz (380 g) sealed plastic bags with paper label stapled over the top edge of each package, 12 packages per case. UPC 44107 10062. Mfg. by The Truck Farm, LLC. Las Cruces, NM 88005.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0069-2020·2019-10-30

    Kenzen Calcium Complex Recalled for Missing Milk Allergen Labeling

    HP Ingredients is recalling Kenzen Calcium Complex tablets because the label lacks the required 'Contains: milk' advisory.

    Product
    NIKKENWELLNESS KENZEN brand Calcium Complex Dietary Supplement 60 Tablets. Label reads "Contains ingredients derived from dairy" under Recommended Use.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0070-2020·2019-10-30

    Hall Global Recalls OXZGEN CBD Capsules for Labeling Errors

    Hall Global, LLC is recalling OXZGEN Performance CBD capsules because the label fails to declare Yellow #6 and lists an incorrect amount of Vitamin B2.

    Product
    OXZGEN Performance 25 mg Hemp Derived CBD + Teacrine + BCAA Orange Flavored, 5 blast caps, 2.2 FL OZ
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0071-2020·2019-10-30

    Sugar Mill Farms Focused Energy Recalled for Undeclared Yellow #6

    Hall Global, LLC is recalling Sugar Mill Farms Focused Energy hemp extract products because the label fails to declare Yellow #6 and lists incorrect ingredients and flavors.

    Product
    Sugar Mill Farms Focused Energy 25 mg Hemp Extract Berry Flavor 7.25 g 5 blast cap count
    Category
    Food
    Distribution
    0 states
  • LowFDA (Devices)·Z-0192-2020·2019-10-30

    Arrow AGB+ Multi-Lumen CVC Kit Recalled for Incorrect Lidstock Labeling

    Arrow International Inc is recalling 745 units of the AGB+ Multi-Lumen CVC Kit because the lidstock label incorrectly lists the product code and catheter length.

    Product
    Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central circulation by way of subclavian, jugular, and femoral veins Product Code: CDC-42703-1A - Product Usage: The ARROWg+ard Blue PLUS catheter permits venous access to central circulation by way of subclavian,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0061-2020·2019-10-30

    Source Naturals Brain Charge Recalled for Labeling Errors

    Threshold Enterprises Ltd is recalling Source Naturals Brain Charge dietary supplements because the label claims for two ingredients were lower than the actual product formulation.

    Product
    Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets, 60 tablets Manufactured for: Source Natural, Inc. PO Box 2118 Santa Cruz, CA 95062 Item Code: SN2613, SN2614 Item UPC: 021078026136, 021078026143
    Category
    Food
    Distribution
    30 states
  • CriticalFDA (Food)·F-0048-2020·2019-10-23

    Lyons Magnus Recalls Dunkin' Mocha Swirl for Undeclared Milk

    Lyons Magnus, Inc. is recalling Dunkin' Mocha Swirl because the product was mislabeled and contains undeclared milk.

    Product
    Dunkin' Mocha Swirl Prepared Exclusively for Dunkin' Brands Canton, MA 02021 Net Contents 64 FL OZ/1.89L Not For Resale
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0036-2020·2019-10-23

    Gullah Gourmet Recalls Nana's Been a Nut Bread for Missing Walnut Labeling

    Gullah Gourmet, Inc. is recalling 673 bags of Nana's Been a Nut Bread because the ingredient statement does not list walnuts, posing a risk to consumers with walnut allergies.

    Product
    Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag CONTAINS WHEAT AND SOY. MADE ON EQUIPMENT THAT MAKES PRODUCTS CONTAINING WHEAT, EGGS, MILK, SOY AND TREE NUTS. GULLAH BOURMET Inc. CHARLESTON, SC 29407 UPC 6 50305 01045 9
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Drugs)·D-0144-2020·2019-10-23

    Atlas Pharmaceuticals Recalls Ascorbic Acid Injection Due to Corn Source Labeling Error

    Atlas Pharmaceuticals is recalling Ascorbic Acid Sterile Injection Solution vials labeled as 'Non-Corn Source' but actually derived from corn. The recall affects 1,646 vials distributed to healthcare facilities in Arizona and Colorado.

    Product
    Ascorbic Acid Sterile Injection Solution, 500 mg/mL, 50 mL vial, Non-Corn Source, Rx only, Atlas Pharmaceuticals, LLC, 711 E Carefree Hwy, Suite 107, Phoenix, AZ 85085, NDC 71591-500-50.
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Food)·F-0041-2020·2019-10-23

    CTC Food International Recalls Orchids Dried Mushroom for Undeclared Sulfites

    CTC Food International is recalling Orchids Dried Mushroom because it contains undeclared sulfites. The recall covers 28,800 units distributed to eight U.S. states.

    Product
    Orchids Dried Mushroom NET WT. 1 oz. (29G) Product of China UPC 0-74601-00947-2 Distributed by CTC Food International, Inc. Richmond, CA 94804
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0030-2020·2019-10-16

    Madrona Market Hot Cocoa Mix Recalled for Undeclared Soy

    Diamond Crystal Brands is recalling Madrona Market Hot Cocoa Mix because it contains soy lecithin that is not declared on the label.

    Product
    Madrona Market Delicatessen Hot Cocoa Mix, Net Wt. 2 lb (907 g), Distributed by Food Services of America, Inc. Scottsdale, AZ packaged 6 boxes per case.
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0032-2020·2019-10-16

    Gridestone Cafe Swiss Style Cocoa Mix Recalled for Undeclared Soy

    Diamond Crystal Brands is recalling Gridestone Cafe Swiss Style Cocoa Mix because the product contains soy lecithin, which is not declared on the label.

    Product
    Gridestone Cafe Swiss Style Cocoa Mix, Net Wt. 32 OZ (2 lb) 907 g, Distributed by Performance Food Group, Richmond, VA packaged 12 boxes per case.
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0021-2020·2019-10-16

    Ritter Sport KAFFEESPLITTER Chocolate Recalled for Undeclared Milk

    STARK INC. is recalling Ritter Sport KAFFEESPLITTER chocolate bars because they contain undeclared milk, a major food allergen.

    Product
    Ritter Sport KAFFEESPLITTER Chocolate with caramelized coffee beans; Net Weight: 3.5oz / 100g; Ingredients: sugar, cocoa mass, caramelized pieces of coffee beans (sugar, coffee (roasted) (4%), sunflower oil), cocoa butter, butter pure fat, emulsifier: lecithin (soy) May contain t
    Category
    Food
    Distribution
    28 states
  • HighFDA (Food)·F-0031-2020·2019-10-16

    Chef's Companion Chocolate Mousse Mix Recalled for Undeclared Soy

    Diamond Crystal Brands is recalling Chef's Companion Instant Chocolate Mousse Mix because it contains soy lecithin that is not declared on the label.

    Product
    Chef's Companion Instant Chocolate Mousse Mix Net Wt. 1 lb 14 oz (851 g), Dist by Diamond Crystal Brands, Inc. Savannah, GA packaged 8 boxes per case.
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0064-2020·2019-10-16

    Conformis Recalls iTotal Hip Replacement Stems Due to Packaging Error

    Conformis, Inc. is recalling two iTotal Hip Replacement femoral stems because sizes 13 and 15 were packed in each other's packaging.

    Product
    iTotal Hip Replacement System, Model HBS-033-0013-020101, Size 13 Hip-Patient Specific Stem Right
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0108-2020·2019-10-16

    Roche Tina-quant sTfR Assay Recalled for Rheumatoid Factor Interference

    Roche Diagnostics is recalling Tina-quant sTfR assays due to updated claims regarding rheumatoid factor interference.

    Product
    cobas c 311; cobas c 501, 502,and COBAS INTEGRA 400 plus Analyzer/Module-RF interference claims for the sTfR assay Catalog Number: 20763454122
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0065-2020·2019-10-16

    Stryker Neurovascular Recalls 8F Balloon Guide Catheters Due to Packaging Error

    Stryker Neurovascular is recalling 190 8F Balloon Guide Catheters because they were incorrectly packaged in 9F Balloon Guide Catheter packaging. The affected lot was distributed only outside the United States.

    Product
    Stryker Neurovascular, Merci 9F, 80cm, Balloon Guide Catheter, REF 90077, CE 0459, UPN Product No. 90077, UDI #: (01)00815742000771
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0063-2020·2019-10-16

    Conformis iTotal Hip Replacement Stems Recalled for Packaging Error

    Conformis, Inc. is recalling two iTotal Hip Replacement femoral stems (sizes 13 and 15) because they were packed in each other's packaging.

    Product
    iTotal Hip Replacement System, Model HBS-033-0015-020101, Size 15 Hip-Patient Specific Stem Right
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0053-2020·2019-10-16

    Arrow Pediatric Central Venous Catheter Kit Recalled for Labeling Error

    Arrow International Inc. is recalling 3,143 Pediatric Two-Lumen Central Venous Catheterization Kits due to a labeling error on the lidstock.

    Product
    Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, REF AK-25502 Product Usage; Provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0051-2020·2019-10-16

    Repro-Med Systems Recalls Mislabeled Subcutaneous Safety Needle Sets

    Repro-Med Systems is recalling 1,990 pouches of 26-gauge subcutaneous safety needle sets due to mislabeled needle lengths.

    Product
    20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous Safety Needle Sets" Product # RMS22606 - Product Usage: RMS HlgH-Flo Subcutaneous Safety Needle Sets are intended for the delivery of medication to the subcutaneous tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide