The Recall Desk

Hazard

Mis Labeling recalls

9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,606
Critical
160
Severe
588
Most recent
2026-09-09

Of the 9,606 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.

151–175 of 9606

  • HighFDA (Devices)·Z-2008-2025·2025-07-02

    Altivate Reverse Torx Peripheral Screw labeling mismatch recall

    Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because package labeling indicates a different screw size than the product actually included. This mismatch could lead to incorrect surgical implantation.

    Product
    Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number: 506-04-126 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Devices)·Z-2010-2025·2025-07-02

    Altivate Reverse Torx Peripheral Screws Package Labeling Mismatch

    Encore Medical is recalling Altivate Reverse Torx Peripheral screws because the package labeling lists a different screw size than what is actually included in the package.

    Product
    Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 18mm Model/Catalog Number: 506-04-118 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Food)·H-0094-2025·2025-07-02

    Probese Caps dietary supplement recalled for undeclared food dyes

    Probese Caps, a dietary supplement with Iron sold in 90-count bottles, is being recalled because it contains undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) in the gelatin capsules.

    Product
    Probese Caps, dietary supplement with Iron. 90-count bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0095-2025·2025-07-02

    NutriLean Dietary Supplement Contains Undeclared Food Dyes

    Preventics, Inc. dba Legere Pharmaceuticals is recalling NutriLean dietary supplements nationwide because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food dyes, which are not listed on the label.

    Product
    NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0061-2025·2025-07-02

    Windsor brand Extra Course Himalayan Pink Salt Grinder Refill recalled

    Windsor brand Extra Course Himalayan Pink Salt Grinder Refill is being recalled because the quantity of product in each unit does not match the stated weight on the packaging.

    Product
    Windsor brand Extra Course Himalayan Pink Salt Grinder Refill, 255 g, packaged in a glass jar with plastic cap and packed 6 units per case, each unit sold individually; Imported by Windsor Salt Ltd., Pointe-Claire, Quebec H9R 5M9
    Category
    Food
    Distribution
    0 states
  • LowFDA (Food)·H-0062-2025·2025-07-02

    Windsor Brand Extra Coarse Sea Salt Grinder Refill Weight Mismatch

    Windsor brand Extra Coarse Sea Salt Grinder Refill (255 g) does not contain the stated weight of product in each unit. Morton Salt Inc. is recalling 28,820 units distributed in Canada.

    Product
    Windsor brand Extra Course Sea Salt Grinder Refill, 255 g, packaged in a glass jar with plastic lid and packed 6 units per case, each unit sold individually; Imported by Windsor Salt Ltd., Pointe-Claire, Quebec H9R 5M9
    Category
    Food
    Distribution
    0 states
  • LowUSDA FSIS·024-2025·2025-06-27

    Gaiser's Recalls Ready-to-Eat Bologna Due to Undeclared Meat Ingredients

    Gaiser's European Style Provisions is recalling approximately 143,416 pounds of ready-to-eat bologna products because they contain undeclared meat or poultry ingredients.

    Product
    Gaiser's European Style Provisions Inc. — Gaiser's European Style Provisions Inc. Recalls Ready-To-Eat Meat and Poultry Bologna Products Due to Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1941-2025·2025-06-25

    Lago X X-ray instrument recall due to labeling discrepancies

    Spectral Instruments Inc is recalling the Lago X X-ray instrument because its safety and manufacturing date labels do not match FDA requirements.

    Product
    Lago X
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0935-2025·2025-06-18

    Instant Milk Tea Brown Sugar Powder recalled for undeclared milk allergen

    R&M Refresher brand Instant Milk Tea Brown Sugar Flavor is recalled because the ingredients contain milk (Whey Powder, Sodium Caseinate) but the label does not declare milk as an allergen.

    Product
    Instant Milk Tea Brown Sugar Flavor, R&M Refresher brand, B0D725TXQW, net wt. 1lb. Product is sold in 3-pack. Parent ASIN #B0D728CZWS 3-pack ASIN #B0D72FQVDR Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder, Sodium Caseinate***). Product of China. Dis
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0043-2025·2025-06-18

    Atlantic Salmon Portions with Seafood Stuffing Recalled for Undeclared Soy Allergen

    Santa Monica Seafood Company is recalling Atlantic Salmon Portions with Seafood Stuffing due to incorrect labeling that fails to declare soy as an allergen ingredient.

    Product
    Atlantic Salmon Portions with Seafood Stuffing; 16 OZ (1 LB) 454g; Use/Freeze By: JUN.02.25; UPC: 4061459716313
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1940-2025·2025-06-18

    Femoral Nail RIGHT T2 GTN 8x300 mm labeled incorrectly

    Stryker GmbH is recalling Femoral Nail RIGHT T2 GTN 8x300 mm devices because some lots were labeled as left or right but contained the opposite orientation.

    Product
    Femoral Nail, RIGHT T2 GTN 8x300 mm. Catalog Number: 1851-0830S.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0934-2025·2025-06-18

    Instant Milk Tea Powder lacks milk allergen declaration

    R&M Trading LLC is recalling Instant Milk Tea Original Flavor because the label does not declare milk, despite containing whey powder and sodium caseinate, which are milk-derived ingredients.

    Product
    Instant Milk Tea Original Flavor, R&M Refresher brand, B0D71YHZX4, net wt. 1lb. Product is sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D71YHZX4 3-pack ASIN #B0D72BLQRW Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1925-2025·2025-06-18

    Digital Acquisition Box Electrode Placement Labels Applied Backwards

    Natus Neurology has recalled the OBM00002 OBM DAB (Digital Acquisition Box) because electrode placement labels were applied backwards. This may lead to misdiagnosis of seizure location in neonates monitored with the device.

    Product
    Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box) Model/Catalog Number: OBM00002 OBM DAB (Digital Acquisition Box) Software Version: N/A Product Description: OBM00002 OBM DAB (Digital Acquisition Box) Component: N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1939-2025·2025-06-18

    Femoral Nail T2 GTN Left and Right Versions Mislabeled

    Stryker GmbH is recalling certain Femoral Nail T2 GTN devices because some labeled as left version contained right nails, and vice versa. This mislabeling could result in incorrect surgical implantation.

    Product
    Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0931-2025·2025-06-18

    Instant Milk Tea Honeydew Flavor powder lacks milk allergen declaration

    R&M Refresher Instant Milk Tea Honeydew Flavor powder contains milk ingredients (whey powder and sodium caseinate) but does not declare milk on the label, posing an allergen risk to consumers with milk allergies.

    Product
    Instant Milk Tea Honeydew Flavor, R&M Refresher brand, B0D7269JC1, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D7269JC1 3-pack ASIN #B0D726K269 Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powd
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0932-2025·2025-06-18

    Instant Milk Tea Taro Flavor Recalled for Undeclared Milk Allergen

    R&M Refresher brand Instant Milk Tea Powder in Taro Flavor is recalled nationwide because the label does not declare milk, though the product contains Whey Powder and Sodium Caseinate derived from milk.

    Product
    Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLBH, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D72CMLBH 3-pack ASIN #B0D72D6589 Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder,
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0936-2025·2025-06-18

    NOW Nutritional Yeast Powder recalled due to packaging error

    NOW Foods is recalling NOW Nutritional Yeast Powder (10 oz, UPC 7 33739 02460 2) because regular yeast was inadvertently packaged as nutritional yeast.

    Product
    NOW Nutritional Yeast Powder, Nt. Wt. 10oz. UPC 7 33739 02460 2
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2025·2025-06-13

    King Tallow LLC Recalls Beef Tallow Produced Without Federal Inspection

    King Tallow LLC is recalling 353 pounds of beef tallow jars produced without federal inspection. The product was sold in Puerto Rico.

    Product
    King Tallow LLC Recalls Beef Tallow Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0836-2025·2025-06-11

    Seasoned Bread Crumbs Recalled for Undeclared Egg and Milk Allergens

    New Grains Gluten Free Bakery is recalling seasoned bread crumbs because printing quality issues made egg and milk allergen declarations illegible on the label. Consumers with allergies to these ingredients may face serious health risks.

    Product
    Seasoned Bread Crumbs: Gluten-free seasoned bread crumbs, vacuum-sealed clear plastic, 8 oz, bulk Ingredients: White rice flour, Water, Egg, Golden flax seed, Rice bran, Tapioca flour, Honey, Palm fruit oil, Potato flour, Yeast, Xanthan gum, Psyllium husk powder, Sea salt, Butt
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0833-2025·2025-06-11

    Gluten-Free Coconut Macaroon Cookies Recalled for Undeclared Allergens

    NEW GRAINS GLUTEN FREE BAKERY is recalling approximately 50 units of Coconut Macaroon Cookies because label printing quality issues rendered allergen declarations for Egg, Milk, and Soy illegible or missing.

    Product
    Coconut Macaroon Cookie: Gluten-free coconut macaroon cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: Coconut flakes, Sweetened condensed milk, Egg whites, Potato flour, Vanilla, Sea salt. Contains: Egg, Milk, Soy.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0825-2025·2025-06-11

    Gluten-Free Sourdough Bread Recalled for Undeclared Egg Allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling Artisan Sourdough Bread (gluten-free, 32 oz) distributed in Utah because the label does not clearly declare the presence of egg allergen due to poor print quality.

    Product
    Artisan Sourdough Bread: Gluten-free sourdough bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Eggs, Tapioca flour, Sugar, Potato flour, Palm fruit oil, Yeast, Psyllium husk powder, Vinegar, Sea salt, Xanthan gum, Powdered sugar.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0830-2025·2025-06-11

    Gluten-Free Multigrain Bagels Recalled for Undeclared Egg Allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling gluten-free multigrain bagels due to printing defects that render the egg allergen declaration illegible on the package label. The product contains egg and poses a risk to consumers with egg allergies.

    Product
    Multigrain Bagels: Gluten-free multigrain bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Honey, Golden flax seed, Palm fruit oil, Potato flour, Yeast, Sugar, Psyllium husk powder, Rice bran, Sea salt, Xanthan
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0832-2025·2025-06-11

    Frosted Sugar Cookies Recalled for Undeclared Allergens

    New Grains Gluten Free Bakery is recalling Frosted Sugar Cookies because the label does not clearly declare allergens: Egg, Milk, and Soy. The product was distributed in Utah.

    Product
    Frosted Sugar Cookie: Gluten-free frosted sugar cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: White rice flour, Powdered sugar, Butter, Sugar, Palm shortening, Sprinkles, Rice milk, Egg whites, Potato flour, Imitation vanilla, Baking powder, Xanthan gum, Gela
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0838-2025·2025-06-11

    Pecan Caramel Bars Recalled for Undeclared Allergen Labels

    New Grains Gluten Free Bakery is recalling Pecan Caramel Bars sold in Utah because printing quality issues made allergen declarations for egg, milk, and pecans unreadable or missing on the package.

    Product
    Pecan Caramel Bars Individually wrapped in plastic. Ingredients: White rice flour, Sugar, Honey, Pecan pieces, Butter, Eggs, Rice milk, Potato flour, Vanilla, Baking powder, Xanthan gum, Unflavored gelatin, Sea salt Contains: Egg, Milk, Tree nuts
    Category
    Food
    Distribution
    1 state