The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 mis labeling recalls we have scored against our rubric, 161 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 589 (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.

7276–7300 of 9611

  • HighFDA (Food)·F-2114-2014·2014-07-16

    Sorghum & Grits Ice Cream Recalled for Missing Allergen Labels

    Koogee-Queen Anne, LLC is recalling Sorghum & Grits Ice Cream because the product lacked required ingredient and allergen labels, including facility processing warnings.

    Product
    Sorghum & Grits Ice Cream. Manufactured by: Koogee-Queen Anne, LLC, d/b/a The Comfy Cow 2221 Frankfort Ave, Louisville, KY 40206.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-2123-2014·2014-07-16

    Ice Cream Recalled for Missing Allergen and Facility Labeling

    Koogee-Queen Anne, LLC is recalling Brown Butter Peanut Brittle Ice Cream because bulk products lacked labels declaring direct allergens and facility processing information.

    Product
    Brown Butter Peanut Brittle Ice Cream, Manufactured by: Koogee-Queen Anne, LLC, d/b/a The Comfy Cow 2221 Frankfort Ave, Louisville, KY 40206.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2025-2014·2014-07-16

    CareFusion Recalls SmartSite Infusion Sets Due to Unlabeled Filter

    CareFusion is recalling SmartSite Low Sorbing Infusion Sets because the drip chamber contains a 15-micron filter not listed in the instructions, posing a risk of occlusion if used with blood.

    Product
    SmartSite Low Sorbing Infusion Set, Model Codes: 10014855A, 10015861A, 10061661A 14035457 14035485 14046894 14035458
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·F-2150-2014·2014-07-16

    Simply Southern Ice Cream Recalled for Missing Allergen Labels

    Koogee-Queen Anne, LLC is recalling Simply Southern Ice Cream because the bulk product lacked labels declaring direct allergens and facility processing information.

    Product
    Simply Southern Ice Cream, Manufactured by: Koogee-Queen Anne, LLC, d/b/a The Comfy Cow 2221 Frankfort Ave, Louisville, KY 40206.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-2141-2014·2014-07-16

    Pistachio Ice Cream Recalled for Missing Allergen and Ingredient Labels

    Koogee-Queen Anne, LLC is recalling pistachio ice cream sold in Indiana and Kentucky because the product lacked required ingredient and allergen labels.

    Product
    Pistachio Ice Cream, Manufactured by: Koogee-Queen Anne, LLC, d/b/a The Comfy Cow 2221 Frankfort Ave, Louisville, KY 40206.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-2138-2014·2014-07-16

    Java Chip Ice Cream Recalled for Missing Allergen and Ingredient Labels

    Koogee-Queen Anne, LLC is recalling Java Chip Ice Cream because bulk products lacked labels declaring ingredients and allergens.

    Product
    Java Chip Ice Cream, Manufactured by: Koogee-Queen Anne, LLC, d/b/a The Comfy Cow 2221 Frankfort Ave, Louisville, KY 40206.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2032-2014·2014-07-16

    Zimmer EDI Periarticular Plating System Screws Recalled for Lot Commingling

    Zimmer Manufacturing B.V. is recalling 496 bone screws because two lots were commingled and packaged with incorrect labels.

    Product
    Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW, FULLY THREADED, HEX HEAD 4MM DIAMETER, 14 MM LENGTH, and EDI 4.0 MM CANCELLOUS SCREW, FULLY THREADED, 20 MM LENGTH. Temporary internal fixation devices, designed to stabilize fractures during the normal healing p
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2024-2014·2014-07-16

    Aesculap Recalls Non-Sterile Sutures With Conflicting Sterile Labeling

    Aesculap is recalling 11 units of non-sterile Dafilon sutures because an additional label incorrectly states the product is sterile.

    Product
    Dafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS, non-sterile, non-absorbable polyamide Surgical Suture, additional label affixed on the box states the product is sterile, packaged in a cassette holding 12 sutures
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Food)·F-2083-2014·2014-07-16

    Cookies Cottage Crispy Taro Cookies Recalled for Undeclared Dyes

    U-Can Food Trading Inc. is recalling Crispy Taro Cookies due to undeclared dyes, including one not permitted for use.

    Product
    The Cookies Cottage (Brand) Crispy Taro Cookies (Toasted Vegetarian Yam Biscuits), 180g. Packaged in 24packets per carton.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2063-2014·2014-07-09

    Jardine Foods Recalls Queso Loco Dip Due to Undeclared Wheat

    Jardine Foods is recalling 14,200 jars of Queso Loco dip because it contains undeclared wheat. The product was distributed in Texas and Canada.

    Product
    DL Jardines Queso Loco (Item#R5230) ; Label: Special Edition D. L. Jardine's Texas Ranch Recipes Queso Loco Cheese Salsa & Dip; Medium; NET WT. 16 OZ (453g); Jardine Foods, Inc.; #1 Chisolm Trail, Buda, Texas 78610; Product of U.S.A.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2068-2014·2014-07-09

    Rite Aid Recalls Thrifty Mint 'N' Chip Ice Cream Due to Undeclared Pistachio

    Rite Aid is recalling 560 pints of Thrifty Mint 'N' Chip ice cream because pistachio was inadvertently packed into the containers without being declared on the label.

    Product
    waxed paperboard int container of frozen ice cream labeled Thrifty Ice Cream Mint 'N' Chip 1 Pint (16 Fl. OZ.) Bottom of container Expiration Date: October 28 2015 Lot #24273 Back of container UPC 1182264327
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-2059-2014·2014-07-09

    Brunkow Monterey Jack Cheese Recalled for Mushroom Mislabeling

    Brunkow Cheese of Wisconsin is recalling Monterey Jack Morel Mushroom & Onion Cheese because it contains a different type of mushroom than listed on the label.

    Product
    Brunkow Cheese of Wisconsin, Monterey Jack Morel Mushroom & Onion Cheese, 5 lb block plastic wrapped and vacuum sealed. Eight blocks per case. Ingredients: Cultured Pasteurized Whole Milk, Salt, Microbial Enzymes, Morel Mushroom and Onion.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1836-2014·2014-07-09

    Claymount Harmony2 Grid Cabinet Recalled for Labeling and Insulation Defects

    Claymount Assemblies BV is recalling 12 Harmony2 grid cabinets because they lack required labeling information and have non-compliant insulation values.

    Product
    The Claymount Harmony is a grid cabinet designed to accept a digital x-ray imaging receptor and stationary grid. It contains signaling electronics to indicate the presence of the grid and detector as well as detector orientation. It may be mounted to a wall stand or incorporated
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Food)·F-2058-2014·2014-07-09

    Roselani Tropics Kona Mud Pie Ice Cream Recalled for Incorrect Contents

    Maui Soda & Ice Works is recalling 2,045 cartons of Roselani Tropics Kona Mud Pie Ice Cream because a complaint reported the cartons contained chocolate Macadamia Nut Ice Cream instead.

    Product
    Roselani Tropics Kona Mud Mud Pie Ice Cream: 1.75QT, - 56 oz. carton. Maui Soda & Ice Works, Ltd. Wailuku, HI
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1984-2014·2014-07-09

    Synthes B37 Replacement Screws Recalled for Potential Mislabeling

    Synthes, Inc. is recalling 44 B37 Replacement Screws because the package may not contain the screws identified on the label.

    Product
    Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming arm, part numbers 3.113.025 and 03.113.026. Surgical instrument for use with Low Bend Medial Distal Tibia Plate. Orthopedic.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1958-2014·2014-07-09

    Focus Diagnostics Recalls Simplexa Flu A/B & RSV Direct Assay Kits

    Focus Diagnostics is correcting labeling for 614 Simplexa Flu A/B & RSV Direct kits due to sporadic false signals that may increase false results.

    Product
    Simplexa" Flu A/B & RSV Direct, Model Number: MOL2650. 510(k) K120413  Simplexa" Flu A/B & RSV Direct. The Focus Diagnostics Simplexa Flu A/B & RSV Direct assay is intended for use on the 3M Integrated Cycler instrument for the in vitro qualitative detection and differe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1972-2014·2014-07-09

    Intuitive Surgical Recalls da Vinci Surgical System Quick Reference Guides

    Intuitive Surgical is recalling Quick Reference Guides for the da Vinci Surgical System to remove the Emergency Grip Release Wrench from instructions.

    Product
    IRK QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System and Si-e. Intuitive Surgical Endoscopic Instrument Control System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1943-2014·2014-07-09

    Blue Belt Technologies Recalls Mislabeled Stride Femoral Knee Components

    Blue Belt Technologies is recalling two lots of Stride Femoral Knee Components due to packaging mislabeling that could lead to the implantation of the wrong side or size.

    Product
    Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2061-2014·2014-07-09

    National Vitamin Recalls Ferrous Gluconate Tablets Due to Mislabeled Iron Content

    National Vitamin Co Inc is recalling Nature's Blend Ferrous Gluconate Tablets because the front panel incorrectly lists 65 mg of elemental iron instead of the correct 36 mg.

    Product
    Ferrous Gluconate Tablets, 5gr (325 mg), Elemental Iron 36 mg, 100 Tablets, UPC 0 79854 50032 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1942-2014·2014-07-09

    Blue Belt Technologies Recalls Mislabeled Stride Unicondylar Knee Prosthesis Components

    Blue Belt Technologies is recalling specific lots of Stride unicondylar knee prosthesis femoral components due to packaging mislabeling that may result in the wrong implant being used.

    Product
    Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1975-2014·2014-07-09

    Intuitive Surgical Recalls da Vinci Surgical System Quick Reference Guides

    Intuitive Surgical is recalling Natural Rubber Latex Quick Reference Guides for the da Vinci Surgical System to update documentation and remove a specific wrench part.

    Product
    Natural Rubber Latex QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Control System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1835-2014·2014-07-09

    Claymount Harmony Grid Cabinets Recalled for Missing Label Information

    Claymount Assembli is recalling Harmony grid cabinets because their labels lack the manufacturer address, date of manufacture, and required compliance statements.

    Product
    The Claymount Harmony is a grid cabinet designed to accept a digital x-ray imaging receptor and stationary grid. It contains signaling electronics to indicate the presence of the grid and detector as well as detector orientation. It may be mounted to a wall stand or incorporated
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-2030-2014·2014-07-02

    Key Lime Dip Recalled for Undeclared Allergens in Compound Ingredients

    Miami Interculinary Center, Inc. is recalling 1,164 bottles of Floribbean Key Lime Calypso Dip because the label failed to declare allergens in compound ingredients.

    Product
    Floribbean Key Lime Calypso Dip 12.5 oz Floribbean 68 SW 40 St. Suite 411 Miami, Florida 33155 1(800)282-8459
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-1847-2014·2014-07-02

    Baxter Abacus 3.1 Pharmacy Calculator Software Field Correction

    Baxter is correcting a software error in Abacus 3.1 that may display protein levels 1,000 times lower than actual when using Clinimix 4.25110.

    Product
    Abacus 3.1, Pharmacy Calculator Product Usage: Provide pharmacy calculations for automated compounding.
    Category
    Medical Device
    Distribution
    Distributed nationwide