The Recall Desk

Hazard

Mislabeling recalls

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

What the numbers show

Total
395
Critical
20
Severe
45
Most recent
2026-07-22

Of the 395 mislabeling recalls we have scored against our rubric, 20 (5%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 45 (11%) 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 mislabeling 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.

26–50 of 395

  • HighFDA (Devices)·Z-1786-2026·2026-04-15

    Cook Medical multipurpose drainage catheters carry overstated expiration dates

    Cook Medical is recalling a Multipurpose Drainage Catheter because affected lots were labeled with expiration dates that exceed the product's true shelf life. 20 units are affected.

    Product
    COOK MEDICAL Multipurpose Drainage Catheter: Reference Part Number ULT8.5-38-25-P-CLMS-8-RH-FS, Order Number G29775
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0652-2026·2026-04-15

    Zarlengo's Double Dark Chocolate Gelato recalled for undeclared soy allergen

    Zarlengo Italian Ice is recalling Zarlengo's Double Dark Chocolate Gelato in 1-gallon buckets because soy lecithin is listed in the ingredients but soy is not disclosed in the allergen statement, posing a risk to consumers with soy allergies.

    Product
    Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper resistant lid.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1785-2026·2026-04-15

    Cricothyrotomy catheter sets labeled with overstated expiration dates

    Cook Incorporated is recalling Melker Universal Cuffed Emergency Cricothyrotomy Catheter Sets because affected lots were labeled with expiration dates that exceed the true shelf life.

    Product
    Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set: Reference Part Number C-TCCSB-500-UNI, Order Number G32193; Reference Part Number C-TCCSB-500-UNI-01, Order Number G47665.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1773-2026·2026-04-15

    Xtant pedicle screws mislabeled with an incorrect shorter screw length

    Xtant Medical is recalling Xpress Pedicle Screw System dual lead screws from one lot that were mislabeled with a part number identifying them as shorter than they physically are.

    Product
    XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1777-2026·2026-04-15

    Cook Medical CTO-18 wire guides labeled with overstated expiration dates

    Cook Medical is recalling Approach CTO-18 Micro Wire Guides because affected lots were labeled with expiration dates that exceed the product's true shelf life. 75 units are affected.

    Product
    COOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-18G, Order Number G50788; Reference Part Number CMW-14-300-18G, Order Number G50792
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·H-0644-2026·2026-04-08

    Mama Rose's Prickly Pear Salad Dressing recalled for undeclared sulfites

    The Maros Group, LLC is recalling Mama Rose's Prickly Pear Salad Dressing (12 oz bottles) distributed in Arizona because the product contains undeclared sulfites, which can pose a health risk to people with sulfite sensitivity.

    Product
    Mama Rose's Prickly Pear Salad Dressing. 12 oz (340 g) glass bottle with gold cap.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0615-2026·2026-04-01

    Savannah Bee Company Honey BBQ Sauce Mustard Undeclared Allergens

    Savannah Bee Company is recalling Honey BBQ Sauce Mustard bottles containing an undeclared different flavor product with soy and wheat allergens not listed on the label.

    Product
    SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES. INGREDIENTS: MUSTARD (DISTILLED VINEGAR, WATER, MUSTARD SEED, SALT, SPICES (INCLUDING PAPRIKA AND TUMERIC), NATURAL FLAVOR, GARLIC), HONEY, WATER, DISTILLED VINEGAR, SUGAR, TOMATO CONCENTRATE, HA
    Category
    Food
    Distribution
    45 states
  • ModerateNHTSA·26V179000·2026-03-24

    2024–2026 Toyota and Lexus vehicles load carrying capacity label incorrect

    Toyota is recalling certain 2024–2026 Toyota and Lexus vehicles because the load carrying capacity modification label may display inaccurate added weight values. Vehicles with incorrect maximum capacity weight may be overloaded, increasing crash risk.

    Product
    TOYOTA — TOYOTA, LEXUS SEQUOIA HYBRID, TUNDRA, TUNDRA HYBRID, redundant TUNDRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0526-2026·2026-03-04

    YO!MAN Lettuce (Spicy Flavor) Recall for Undeclared Cyclamates

    TENGEN USA Trading Corp recalls YO!MAN Lettuce (Spicy Flavor) due to undeclared cyclamates. FDA Class III recall for 26 cases in NY, PA, FL, LA, TX.

    Product
    YO!MAN LETTUCE (SPICY FLAVOR); Ingredients: Lettuce, chili pepper, edible vegetable oil, salt, water, sugar, food additives (monosodium glutamate, potassium sorbate, streptoccoccus lactis, sodium dehydroacetate, sodium D-isoacsorbate, disodium ethylenediaminetetraacetatic acid,
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·H-0330-2026·2025-12-31

    Coffee cake recalled after maple walnut was labeled as raspberry

    The James Skinner LLC is recalling 811 cases of Publix Raspberry Coffee Cake because Maple Walnut Coffee Cake was incorrectly labeled as Raspberry and walnuts were not declared.

    Product
    Publix Raspberry Coffee Cake, Net Wt. 15 oz. (425g), packaged in an aluminum foil tray and clear plastic clamshell lid with wraparound label, UPC 0-41415-54691-2, Distributed By Publix Supermarkets, Inc. Lakeland, FL 33802, packed 12 per case Case label reads, in part: Maple Wal
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-0302-2026·2025-12-10

    Protein powder recalled because the label omits milk and claims allergen free

    Genepro Protein is recalling 250 bags of Genepro Whey 4th Generation protein because the labeling contains incorrect ingredient information and fails to declare milk as an allergen.

    Product
    Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable mylar bag, UPC 850053365126, Manufactured For: Genepro Protein, Inc. 15000 Weston Parkway, Cary NC 27513 Front label reads, in part: "* LACTOSE FREE * DAIRY FREE *
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Food)·H-0184-2026·2025-10-29

    Shanghai style noodles recalled for undeclared egg and two color additives

    Twin Marquis is recalling 5,080 packages of Thick Shanghai Style Plain Noodle because the product contains undeclared egg, FD&C Yellow 5 and FD&C Yellow 6.

    Product
    Twin Marquis brand THICK SHANGHAI STYLE PLAIN NOODLE; NET WT 16 OZ; Ingredients: Bleached Wheat Flour, Water, Corn Starch, Salt, Sodium Benzoate (For Freshness); Contains: Wheat.; Produced on machinery that uses eggs; Manufactured by: Twin Marquis Inc. Brooklyn, NY 11206; UPC 7 6
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·H-0127-2026·2025-10-29

    Dubai style chocolate recalled because wheat is not declared as allergen

    Rolling Pin Baking Company is recalling 127,680 units of Rolling Pin Dubai Style Chocolate because the product does not declare wheat in the allergen statement.

    Product
    Rolling Pin brand Dubai Style Chocolate; 17.64 oz stand up pouch; Ingredients: Sugar, Cocoa Butter, Vegetable Fats, Whole Milk Powder, Pistachio (Tree Nut), Skimmed Milk Powder, Cocoa Mass, Kunefa, Soy Lecithin, Natural Vanilla Powder; Allergens: Contains Milk, Soy, Nuts (Pistach
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·H-0099-2026·2025-10-29

    Pecan caramel clusters recalled because they may contain undeclared cashews

    Abdallah Incorporated is recalling 744 units of Lunds & Byerly's Pecan Caramel Clusters because the product may contain undeclared cashews.

    Product
    Lunds & Byerly's Premium confections. Pecan Caramel Cluster Dipped in milk chocolate. Net Wt 2.5 oz (71g) UPC 0 72431-01294 5. Produced for Lunds & Byerlys, Edina, MN 55424.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0229-2026·2025-10-29

    Locking bone screws recalled after packaging labeled with the wrong length

    Synthes is recalling 122 low profile locking screws because 42mm screws were packaged and labeled as 46mm and 46mm screws were labeled as 42mm, though the etched length is correct.

    Product
    LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 42MM / XL25/ STER. Product Code: 04.045.342TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0228-2026·2025-10-29

    Forty six millimetre locking screws recalled over wrong length on packaging

    Synthes is recalling 120 low profile locking screws because 42mm screws were packaged and labeled as 46mm and 46mm screws were labeled as 42mm, though the etched length is correct.

    Product
    LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 46MM / XL25/ STER. Product Code: 04.045.346TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0032-2026·2025-10-29

    Cetirizine hundred count bottles recalled over tablets imprinted with wrong identifier

    JB Chemicals is recalling 9,936 hundred-count bottles of Cetirizine Hydrochloride Tablets USP 10 mg because the tablets were imprinted with the wrong identification code.

    Product
    CETIRIZINE HYDROCHLORIDE — CETIRIZINE HYDROCHLORIDE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide