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.

4101–4125 of 9607

  • LowFDA (Food)·F-0522-2018·2017-12-27

    New Century Snacks Recalls Mixed Nuts Due to Incorrect Back Panel Labeling

    New Century Snacks LLC is recalling Happy Belly Deluxe Mixed Nuts because the back panel ingredients and nutrition facts were incorrect. The principal display label correctly lists the main allergens.

    Product
    Happy Belly Deluxe Mixed Nuts - roasted and salted with sea salt. Cashews, Almonds, Brazil nuts, pecans & Hazelnuts 16 oz. (454 g); Allergen information: contains Milk, Almonds, Wheat, Peanuts. UPC 48719 09577 Cranberry & Nuts Trail mix has dried cranberries, cashew & a
    Category
    Food
    Distribution
    10 states
  • LowFDA (Food)·F-0500-2018·2017-12-27

    Hain Celestial Recalls BluePrint Organic Beet Blast Drinks Due to Labeling Error

    The Hain Celestial Group is recalling 1,949 cases of BluePrint Organic Beet Blast Vegetable & Fruit Drink because the label on the back of the bottle may be for the incorrect product.

    Product
    BluePrint ORGANIC Beet Blast Vegetable & Fruit Drink 16 fl.oz.(473mL) USDA Organic. Keep Refrigerated.
    Category
    Food
    Distribution
    13 states
  • LowFDA (Food)·F-0523-2018·2017-12-27

    New Century Snacks Recalls Happy Belly Cranberry and Nuts Trail Mix

    New Century Snacks LLC is recalling Happy Belly Cranberry & Nuts Trail Mix because the back panel ingredients and nutrition facts were incorrect.

    Product
    Happy Belly Cranberry & Nuts Trail Mix - dried cranberries, cashews and almonds. 16 oz. (454 g); Allergens: almonds, Cashews UPC 48719 09587 Cranberry & Nuts Trail Mix - Dried cranberries (cranberries, sugar, sunflower oil), cashews, almonds, vegetable oil (may contain one
    Category
    Food
    Distribution
    10 states
  • LowFDA (Devices)·Z-0268-2018·2017-12-27

    Philips SureSigns Vital Signs Monitors Recalled for Labeling Error

    Philips is recalling SureSigns VSi and VS2+ vital signs monitors because some units have a placeholder date of manufacture instead of the specific date.

    Product
    Philips SureSigns VSi / SureSigns VS2+ vital signs monitor used in healthcare environments and transport within a facility.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0491-2018·2017-12-20

    Wang Globalnet Fish Cake Recalled for Undeclared Egg and Wheat

    Wang Globalnet is recalling Fish Cake in Polybag due to undeclared egg and wheat allergens. The product was distributed across 11 states.

    Product
    Fish Cake in Polybag 10/2.2lbs, Item no. 12842 UPC Code 087703128422
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0239-2018·2017-12-20

    FDA Recalls Piranha Cervical Spine Screws Due to Incorrect Length Marking

    The FDA is recalling 82 Piranha screws used in cervical spine surgery because some units marked as 12 mm actually measure 14 mm.

    Product
    Piranha Screw 4.0 x 12mm, used in Piranha Surgical Plate System The Piranha Surgical Plate System is intended to provide stabilization of the cervical vertebrae for various indications as part of the Omni Spine Anterior Cervical Plate System. The Omni Spine Anterior Cervical P
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0479-2018·2017-12-20

    First Source Recalls Dark Chocolate Almonds for Undeclared Milk

    First Source, LLC is recalling Dark Chocolate Almonds sold under multiple brands because the products contain undeclared milk.

    Product
    Dark Chocolate Almonds packaged under the brand names: (1)Wegmans, 23 OZ (1 LB 7 OZ) 652g tub UPC: 0 77890 328200 4 and 11.5 oz. (326g) tub UPC: 0 70784 50743 9; (2)Alpine Valley 11.5 OZ (326 g). tub UPC 0 23637 41099 8; (3)Tops 11.5oz . tub (326 g) UPC: 0 70784 50743 9; (4) C
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·F-0442-2018·2017-12-20

    Colorado Nut Co Recalls Oat Bran Nutty Crunch for Undeclared Milk

    Colorado Nut Co is recalling Oat Bran Nutty Crunch snack mix because it contains undeclared milk, a major food allergen.

    Product
    Oat Bran Nutty Crunch (8 oz. bag), UPC 018142352130. Packaged in Plastic Zip Lock bags. No refrigeration needed.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-0455-2018·2017-12-20

    Kellbran Drizzled Vanilla Popcorn Recalled for Undeclared Soy Allergen

    Kellbran Candies and Snacks Inc is recalling 520 bags of Drizzled Vanilla Popcorn because soy was not declared in the ingredient statement.

    Product
    DRIZZLED VANILLA POPCORN Net Wt. 3 oz (84.9g) Ingredients: Popcorn, corn syrup, sugar, lecithin***ALLERGY INFO: Manufactured in a facility that processes Milk, Wheat, Soy, Tree Nuts, Peanuts Stew Leonard's 100 Westport Ave., Norwalk, CT
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·17V831000·2017-12-20

    Toyota Recalls Vehicles with Incorrect Load Capacity Labels

    Toyota is recalling 2017-2018 models due to incorrect load carrying capacity labels that may lead to vehicle overloading and increased crash risk.

    Product
    TOYOTA — TOYOTA, LEXUS TUNDRA, 4RUNNER, SIENNA, TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0231-2018·2017-12-20

    Radiometer ABL800 Analyzer Recalled for Barcode Misinterpretation

    Radiometer America Inc. is recalling 1,749 ABL800 analyzers because a barcode scanner error may display results from a different patient.

    Product
    ABL800 analyzer with FLEXQ module. Device intended for in vitro testing of samples of whole blood for the parameters pCO2, cK+, cNa+, cCa2+, cCl , cGlu, cLac, cCrea, ctBil, and co-oximetry parameters (ctHb, sO2, and the hemoglobin fractions FO2Hb, FCOHb, FMetHb, FHHb and FHbF)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0187-2018·2017-12-20

    Physio-Control Recalls LIFEPAK Electrode Starter Kits Due to Labeling Errors

    Physio-Control is recalling 14,219 LIFEPAK Electrode Starter Kits because the infant artwork shows incorrect pad placement and is missing required warning symbols.

    Product
    LIFEPAK(R) Electrode Starter Kits, Catalog # 11101-000017, MIN #3202784-009 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0186-2018·2017-12-20

    Physio-Control Recalls Defibrillation Electrodes Due to Incorrect Pad Placement Artwork

    Physio-Control is recalling 14,219 LIFEPAK defibrillation electrodes because the artwork instructs incorrect pad placement and is missing required warning symbols.

    Product
    LIFEPAK(R) defibrillation electrodes, Catalog # 11101-000016, MIN #3202380-006 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0486-2018·2017-12-20

    Gourmet International Recalls Premio Strawberry Pralinati for Undeclared Colors

    Gourmet International Inc. is voluntarily recalling Premio Strawberry Pralinati cookies due to undeclared colors. The recall covers 24,179 cases distributed in several US states.

    Product
    Premio Strawberry Pralinati, Strawberry with Cocoa, 3.53oz, 10 units per case, packed in Paper Cartons
    Category
    Food
    Distribution
    13 states
  • ModerateNHTSA·17V828000·2017-12-18

    Mercedes-Benz Recalls GLE 550e Vehicles for Incorrect Tire Pressure Labels

    Mercedes-Benz is recalling 2016-2017 GLE 550e 4MATIC vehicles because the B-pillar tire pressure label lists incorrect seating capacity and tire dimensions, violating federal safety standards.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE550E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E073000·2017-12-14

    AP Racing Recalls Super 600 Brake Fluid Due to Missing Label Information

    AP Racing is recalling 16.9oz bottles of Super 600 Brake Fluid because the labels are missing required DOT information regarding track-only use and fluid type.

    Product
    SERVICE BRAKES, HYDRAULIC:FLUID recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0102-2018·2017-12-13

    Pravastatin Tablets Recalled Due to Incorrect Bupropion Filling

    International Laboratories is recalling Pravastatin Sodium Tablets 40 mg because they were filled with Bupropion hydrochloride XL Tablets 300 mg.

    Product
    Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-925-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0446-2018·2017-12-13

    Plow and Hearth Recalls Chocolate Covered Cashews Due to Undeclared Peanuts

    Plow and Hearth is recalling 1,332 units of 10-ounce Cashew Towers because the product contains salted peanuts instead of cashews, posing an undeclared allergen risk.

    Product
    89291 Cashew Tower (Plow and Hearth Chocolate Covered Cashews). Net weight: 10 ounces . The product is package as a Individual can is sealed tin with a plastic lid / Tower is packaged in a clear acetate (plastic) sleeve.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0420-2018·2017-12-13

    Plow & Hearth Chocolate Covered Cashews Recalled for Undeclared Peanuts

    Virginia Diner Inc. is recalling 60 cans of Plow & Hearth Chocolate Covered Cashews because peanuts were found in the product, posing a risk to individuals with peanut allergies.

    Product
    Plow & Hearth Chocolate Covered Cashews
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0433-2018·2017-12-13

    Meijer Cashews Recalled for Undeclared Mixed Nuts

    Meijer Distribution is recalling specific lots of cashews that contain undeclared mixed nuts instead of chocolate covered cashews.

    Product
    Roasted & Salted Cashews and Chocolate Covered Cashews; packaged in clear plastic containers; NET WT 18 oz. (1 LB 2 oz.), 510 g; UPC 8-86926-46877-9
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0199-2018·2017-12-13

    DeRoyal Surgical Kits Recalled for Incorrect Expiration Date on Prep Pads

    DeRoyal is recalling sterile custom surgical kits containing Medline Aplicare Povidone Iodine Prep Pads due to incorrect expiration dates.

    Product
    DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep Pads: a) Incision and Drainage Tray, REF 47-763.04 b) Incision and Drainage Tray, REF 47-763.06 c) Incision and Drainage Tray, REF 47-763.07 d) Cricothyreotomy Ambulance Kit, REF 89-6752.01 e) Incis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0209-2018·2017-12-13

    Remel Mueller-Hinton Broth Recalled for Incorrect Cation Labeling

    Remel Inc is recalling 7 units of Mueller-Hinton Broth IVD because the product label may contain incorrect cation information.

    Product
    CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0211-2018·2017-12-13

    Biosense Webster Recalls PENTARAY NAV High-Density Mapping Catheters

    Biosense Webster is recalling PENTARAY NAV High-Density Mapping Catheters because the instructions for use were updated to indicate they should not be used in patients with prosthetic valves.

    Product
    PENTARAY NAV High-Density Mapping Catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0212-2018·2017-12-13

    Biosense Webster Recalls PENTARAY NAV Mapping Catheters Due to Labeling Update

    Biosense Webster is recalling 73,796 PENTARAY NAV High-Density Mapping Catheters to update contraindication language in the Instructions For Use regarding prosthetic valves.

    Product
    PENTARAY NAV High-Density Mapping Catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0201-2018·2017-12-13

    Exactech Recalls Vantage Total Ankle Tibial Inserts Due to Labeling Mismatch

    Exactech, Inc. is recalling nine Vantage Total Ankle Tibial Inserts because the inner labeling and packaged device may not match the outer box label.

    Product
    Vantage Total Ankle Tibial Insert, Fixed Bearing, 10 mm, Left, Size 3. Exactech Inc. Intended for patients with ankle joints damage by severe rheumatoid, post-traumatic, or degenerative arthritis. It is also indicated for revision of failed previous reconstructions where suffi
    Category
    Medical Device
    Distribution
    1 state