The Recall Desk

Hazard

Mis Labeling recalls

1,381 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

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.

176–200 of 1381

  • SevereFDA (Food)·H-0511-2025·2025-08-27

    Blueberry Fritter Recalled Due to Undeclared Egg Allergen

    Hillside Orchard Farms is recalling Blueberry Fritters due to undeclared egg. The product was distributed to five states and poses a risk to consumers with egg allergies.

    Product
    Blueberry Fritter Net Wt 7 oz (198g) CONTAINS: MILK, SOY, WHEAT. Made By: Hillside Orchard Farms 105 Mitcham Circle Tiger, GA 30576
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·H-0504-2025·2025-08-27

    7up Zero Sugar Tropical Soda Recalled for Incorrect Sugar Content Labeling

    Buffalo Rock Company is recalling 7up Zero Sugar Tropical Soda because cans labeled as zero sugar actually contain full sugar. The recall affects 1954 cases distributed in Alabama, Florida, and Georgia.

    Product
    7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up Tropical Flavored Soda, UPC (on can): 078000037975, UPC (on carton): 078000037982
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2345-2025·2025-08-27

    Dynex Agility Sample Tips Misidentified Due to Incorrect Internal Labeling

    Dynex Agility Sample Tips (Model 67910) have incorrect internal labeling that causes the instrument to misidentify them as a different tip type. This incompatibility prevents use and delays patient test results.

    Product
    Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used with the Agility Automated ELISA system.
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·H-0463-2025·2025-08-20

    La Michoacana Coconut Con Crema Paleta recalled for undeclared milk allergen

    Tropicale Foods is recalling La Michoacana Coconut Con Crema 6-Pack Paletas due to missing milk allergen declaration on the label. Consumers with milk allergies should not consume this product.

    Product
    La Michoacana Coconut Con Crema 6-Pack Paleta 16.5oz UPC: 7-67778-00101-0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0469-2025·2025-08-20

    Helados Mexico Minis Variety Paletas recalled for undeclared milk allergen

    Tropicale Foods recalls Helados Mexico Minis Variety Paletas nationwide due to undeclared milk allergen. The product label lists cream as an ingredient but fails to disclose milk as the source, posing a risk to milk-allergic consumers.

    Product
    Helados Mexico Minis Variety Paletas 12-Count 18oz UPC:6-82082-61215-1
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0453-2025·2025-08-20

    Soda Biscuits Recalled for Undeclared Milk and Wheat Allergens

    Soda Biscuits (Rye Flavor) are being recalled due to mislabeling—they do not declare milk powder and wheat allergens. The recall affects 4800 units distributed to California supermarket wholesalers.

    Product
    Soda Biscuit (Rye Flavor), Net Wt: 360g/12.07oz; Shelf life: 10 months; Manufacturer: Zhejiang Dinggian Industrial Co., Ltd. Importer: Shang Hao Jia., Inc. UPC: 6 970425 865055
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0466-2025·2025-08-20

    La Michoacana Paletas Recalled for Undeclared Milk Allergen

    La Michoacana Variety Paletas are being recalled because the label lists CREAM but fails to declare Milk as an allergen source. The recall affects consumers with milk allergies nationwide.

    Product
    La Michoacana Variety Paletas 16-Count 44oz UPC:7-67778-03100-0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2280-2025·2025-08-20

    Cannulated Fenestrated Polyaxial Screws Recalled for Incorrect Labeling

    SPINEART SA is recalling certain Cannulated Fenestrated Polyaxial Screws (PERLA TL MIS) due to incorrect labeling. The affected devices were distributed in Florida, Kentucky, and California.

    Product
    Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S Software Version: Not Applicable Product Description: CANNULATED FENESTRATED POLYAXIAL SCREW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0461-2025·2025-08-20

    Bubble Gum Paleta Recall: Missing Milk Allergen Label

    La Michoacana Bubble Gum paletas are being recalled because the product label lists cream as an ingredient but fails to disclose milk as the allergen source, posing a risk to consumers with milk allergies.

    Product
    La Michoacana Bubble Gum Single Serve Paleta 3.75oz UPC: 7-67778-00003-7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0489-2025·2025-08-20

    Wheat Hamburger Buns Recalled for Undeclared Milk and Egg Allergens

    The Bonami Baking Company is recalling Wheat Hamburger Buns containing undeclared milk and/or eggs not listed on the label. Consumers with allergies to milk or eggs should not consume this product.

    Product
    Wheat Hamburger Buns --- Ingredient Declaration: Water, Whole Wheat Flour, Enriched Wheat Flour (Unbleached Wheat Flour, Malted Barley Flour, Niacin, Iron, Thiamin Mononitrate (Vitamin B1) Riboflavin (Vitamin B2), Folic Acid) Eggs, Butter (Pasteurized Cream, Natural Flavorings),
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0459-2025·2025-08-20

    La Michoacana Strawberry Paleta Recalled for Undeclared Milk Allergen

    Tropicale Foods is recalling La Michoacana Strawberry Con Crema Paletas nationwide due to missing milk allergen declaration on the label. The product contains cream but fails to identify milk as its source allergen.

    Product
    La Michoacana Strawberry Con Crema Single Serve Paleta 3.75oz UPC: 7-67778-00002-0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0471-2025·2025-08-20

    Helados Mexico Choco-Dipped Minis Paletas recalled for undeclared milk allergen

    Tropicale Foods is recalling Helados Mexico Choco-Dipped Minis Variety Paletas nationwide due to missing milk allergen declaration. The product contains cream but does not identify milk as an allergen source.

    Product
    Helados Mexico Choco-Dipped Minis Variety Paletas 12-Count 18oz UPC: 6-82082-81215-5 UPC: 6-82082-41215-7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0487-2025·2025-08-20

    Whole Grain Jalapeno Cheddar Bagels Recalled for Undeclared Milk Allergen

    The Bonami Baking Company is recalling Whole Grain Par Baked Jalapeno Cheddar Bagels because the label does not declare milk as an allergen, despite milk being present in the cheddar cheese ingredient. Consumers with milk allergies are at risk.

    Product
    Whole Grain Par Baked Jalapeno Cheddar Bagel --- Ingredient Declaration: Whole White Wheat Flour, Enriched Flour (Unbleached Wheat Flour, Malted Barley Flour, Niacin, Iron, Thiamine Mononitrate (Vitamin B1), Riboflavin (Vitamin B2), Folic Acid) Water, Brown Sugar, Malt Extract, S
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2289-2025·2025-08-20

    Plastic Trial Head Surgical Device Recalled for Inconsistent Labeling

    Waldemar Link GmbH recalls plastic trial head components due to inconsistent size terminology and color coding on labeling. The inconsistency could lead to incorrect component selection during surgical procedures.

    Product
    Plastic Trial Head Brown, 7 mm neck length. Item Number: 175-928/15.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2286-2025·2025-08-20

    EMPOWR 3D Knee Implants Recalled for Incorrect Size and Side Labeling

    Encore Medical recalled 40 EMPOWR 3D knee implants because labels incorrectly specified implant size and/or side. The affected implants were distributed nationwide and patients should contact their healthcare provider if concerned.

    Product
    Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 7R 16MM, VE Model/Catalog Number: 342-16-707 Product Description: Enovis knee devices are intended for treatment of patients who are candidates for knee arthroplasty per the Indication for use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0465-2025·2025-08-20

    La Michoacana Minis Paletas recalled for undisclosed milk allergen

    Tropicale Foods recalls La Michoacana Minis Variety Paletas due to missing milk allergen disclosure on the label. The product lists cream as an ingredient but does not identify milk as the allergen source.

    Product
    La Michoacana Minis Variety Paletas 12-Count 16.5oz UPC: 7-67778-03042-3
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0442-2025·2025-08-20

    Lithium Orotate Supplement Recalled Due to Potency Deficiency

    Enjoy Nutrition LLC recalls Lithium Orotate 1MG supplements nationwide due to potency deficiency. The product fails to meet labeled lithium orotate strength.

    Product
    Lithium Orotate, 1MG, Distributed by Enjoy Nutrition, LLC. UPC#: 717340952714
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0441-2025·2025-08-20

    Actylis Brand Lithium Orotate Recalled for Lower Potency

    Aceto US is recalling Actylis brand Lithium Orotate 4% and 9% products because the potency levels are lower than labeled. The 4% product contains only 3%, and the 9% product contains 4.45%.

    Product
    a.) Actylis brand Lithium Orotate 4% packaged in HDPE Liner in a 25kg carton b.) Actylis brand Lithium Orotate 9% packaged in HDPE Liner in a 25kg carton
    Category
    Drug
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-2324-2025·2025-08-20

    Anorectal Manometry Procedure Kit Recalled for Mislabeled Expiration Date

    Diversatek Healthcare is recalling the Zvu Anorectal Manometry Procedure Kit (Lot 24752) because the outer kit label displays an incorrect expiration date using the manufacturing date instead. The correct expiration date appears on inner kit labels.

    Product
    Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2279-2025·2025-08-20

    Cannulated Fenestrated Polyaxial Screws Recalled Due to Incorrect Labeling

    SPINEART SA is recalling PERLA TL MIS Cannulated Fenestrated Polyaxial Screws (Model MPF-PS 65 40-S, Lot 8-4528) due to incorrect labeling. Affected units were distributed nationwide in Florida, Kentucky, and California.

    Product
    Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 65 40-S Software Version: Not Applicable Product Description: CANNULATED FENESTRATED POLYAXIAL SCREW Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·25434·2025-08-14

    Firefly Safe & Green 32 oz. Fuel Bottles Recalled for Poisoning Risk

    Firefly Safe & Green 32 oz. fuel bottles have a nozzle applicator that is not child-resistant. The product poses a hydrocarbon poisoning hazard to young children and is incorrectly labeled as non-toxic.

    Product
    Firefly Safe & Green 32 oz. Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2176-2025·2025-08-13

    B. Braun Medical IV Extension Set Labeled with Incorrect Filter Description

    B. Braun Medical is recalling 34,825 Microbore Extension Sets due to incorrect labeling claiming air-eliminating capability the device does not possess.

    Product
    Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.
    Category
    Medical Device
    Distribution
    32 states
  • LowFDA (Food)·H-0388-2025·2025-08-13

    Boar's Head Chevre Goat Cheese Recalled for Incorrect Package Label Date

    Stickney Hill Dairy recalls Boar's Head Chevre Goat Cheese Cranberry Cinnamon due to an incorrect Use By date printed on the package. The recall affects 372 cases distributed in New York.

    Product
    Boar's Head Chevre Goat Cheese Cranberry Cinnamon, Net Wt 4 oz (113g). UPC 0 42421-15231 9. Keep Refrigerated. Distributed By: Brunckhorst Co., NY, NY 11206-3886.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-0348-2025·2025-08-06

    Lespoir cookies recalled for undeclared milk allergen

    Lespoir cookies by Jalux America contain undeclared milk, a common allergen. The recall affects products with a Best Before date of September 26, 2025, sold in California, Illinois, and Washington.

    Product
    Lespoir cookie, net weight: 1.41 oz. UPC# 4 942737 200147
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0358-2025·2025-08-06

    Reisman's Jumbo Pink & White Cookies 3 oz. recalled for undeclared wheat

    Reisman Bros Bakery is recalling Reisman's Jumbo Pink & White Cookies 3 oz. due to undeclared wheat. The product poses a risk to consumers with wheat allergies or celiac disease.

    Product
    Reisman's Jumbo Pink & White Cookies 3 oz.
    Category
    Food
    Distribution
    9 states