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.

676–700 of 9606

  • ModerateFDA (Food)·F-1532-2023·2023-09-27

    Refrigerated Cheese Products Recalled for Unclear Refrigeration Label Requirements

    Great Lakes Cheese, Inc. is recalling refrigerated cheese products because product labels have varying refrigeration requirements that could lead to improper storage. Approximately 7.2 million lbs of products sold under Clancy's and Hill Country Fare brands are affected.

    Product
    Pasteurized Prepared Cheese Product, Queso Blanco, Half the Fat of Cheddar Cheese packaged under the following brands and sizes: 1. Clancy's CheeseMelt, Net Wt 32 oz (2 lbs) 907g. Refrigerate after Opening. Dist, & Sold exclusively by: Aldi, Batavia, IL 60510 2. Hill Cou
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1531-2023·2023-09-27

    Pasteurized Cheese Product Recalled for Inconsistent Refrigeration Instructions on Labels

    Great Lakes Cheese, Inc. is recalling Hill Country Fare Melt'n Cheese because product labels contain inconsistent refrigeration requirements, which may result in improper storage by consumers.

    Product
    Hill Country Fare Melt'n Cheese, Pasteurized Prepared Cheese Product, Net Wt 32 oz (2 lbs) 907g. UPC 0 41220-77273 5. Refrigerate after Opening. Distributed By: H-E-B, San Antonio, TX 78204
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1530-2023·2023-09-27

    HEB Easy Melt Pasteurized Cheese Spread Recalled for Conflicting Refrigeration Labels

    Great Lakes Cheese is recalling HEB Easy Melt Original Pasteurized Process Cheese Spread because refrigeration instructions vary across product labels. No illnesses have been reported.

    Product
    Pasteurized Process Cheese Spread packaged under the following brands and sizes: 1. HEB Easy Melt Original, Net Wt 16 oz (1 lb) 453g. UPC 0 41220-73808 3. Refrigerate after Opening. Made with Pride and Care for H-E-B, San Antonio, Texas 78204 2. HEB Easy Melt Original, Net
    Category
    Food
    Distribution
    32 states
  • HighUSDA FSIS·045-2023·2023-09-23

    Green Valley Foods Recalls Frozen Meat Pizzas Due to Undeclared Soy

    Green Valley Foods is recalling approximately 4,062 pounds of frozen meat pizza products because they contain soy, a known allergen, that is not declared on the label.

    Product
    Green Valley Foods — Green Valley Foods Recalls Frozen Meat Pizza Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1513-2023·2023-09-20

    Natural Products Supplement Recalled Due to Mislabeling with Toxic Plant

    Todorganic Inc. is recalling TODRGANIC Natural Products NUEZ DE LA INDIA (Lot 168, EXP 10/24) because the product contains Yellow Oleander instead of the labeled ingredient. Yellow Oleander is toxic if ingested.

    Product
    TODRGANIC Natural Products, NUEZ DE LA INDIA, Natural Products, 12 Seeds 12 Semillas
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1515-2023·2023-09-20

    Knorr Soup Mix Recalled for Undeclared Egg Allergen

    Conopco is recalling Knorr Fideos con Tomate Tomato Based Pasta Soup Mix because it contains undeclared egg. The product was distributed nationwide with best-by dates through July 6, 2024.

    Product
    Knorr Fideos con Tomate Tomato Based Pasta Soup Mix 3.5 oz UPC: 048001716162
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1511-2023·2023-09-20

    Ritchie's Distribution Pizza Dough Recall Due to Undeclared Soy Allergen

    Cassanos Inc is recalling Ritchie's Distribution Pizza Dough (lots 193, 194) distributed in Ohio due to undeclared soy flour. Consumers with soy allergies should not consume this product.

    Product
    Ritchie's Distribution Pizza Dough on Parchment: packaged as 16in (regular)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2537-2023·2023-09-20

    Ultrasound gel procedural kits recalled for mislabeled use instructions

    Advance Medical Designs is recalling 1880 ultrasound gel procedural kits due to mislabeling that indicates inappropriate use. The affected kits were distributed in the US, Canada, UK, Panama, and the Netherlands.

    Product
    procedural kits containing ultrasonic transmission gel, Item Numbers: a)¿¿¿¿¿ 28-GG023, b)¿¿¿¿ 28-GG105, c)¿¿¿¿¿ 28-GG107, d)¿¿¿¿ 28-GG121, e)¿¿¿¿ 28-GG219, f)¿¿¿¿¿¿ 28-GG223, g)¿¿¿¿¿ 28-GG303, h)¿¿¿¿ 28-GG307, i)¿¿¿¿¿¿ 28-GG519, j)¿¿¿¿¿¿ 28-GG519PC, k)¿¿¿¿¿
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2534-2023·2023-09-20

    Procedural kits with ultrasonic transmission gel recalled for mislabeling

    Advance Medical Designs, Inc. is recalling 26,900 procedural kits containing ultrasonic transmission gel due to mislabeling of use instructions. The affected products were distributed in the U.S., Canada, the UK, Panama, and the Netherlands.

    Product
    Procedural kits containing ultrasonic transmission gel, Item Numbers: a) 20-PMT03, b) 20PMT04
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2536-2023·2023-09-20

    Ultrasound Gel Procedural Kits Recalled for Inappropriate Use Mislabeling

    Advance Medical Designs is recalling procedural kits containing ultrasonic transmission gel because the product labeling does not accurately indicate appropriate use. The recall affects 460 units distributed to the US, Canada, UK, Panama, and Netherlands.

    Product
    Procedural kits containing ultrasonic transmission gel, Item Numbers: a) 28-EG103, b) 28-EG125, c) 28-EG135, d) 28-EG151, e) 28-EG161, f) 28-EG163, g) 28-EG197
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2533-2023·2023-09-20

    Ultrasound gel recalled for mislabeling with inappropriate use instructions

    Advance Medical Designs is recalling 50-GEL20 ultrasound gel (13,750 units, lot 21043C2328) due to mislabeling with inappropriate use instructions. The product was distributed in the US, Canada, UK, Panama, and the Netherlands.

    Product
    50-GEL20; Ultrasound gel
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2579-2023·2023-09-20

    Copaliner Cavity Varnish Recalled for Solvent Mislabeling Error

    Keystone Industries recalls Copaliner Cavity Varnish after discovering bottles of Copaliner Solvent were accidentally packaged in boxes labeled as varnish. The error affected 337 units distributed worldwide.

    Product
    Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to provide a marginal seal between the dentin and amalgam which helps to protect against penetration of amalgam into the dentina Item No. 0921526
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2580-2023·2023-09-20

    Denture relining kit recalled for outer box labeling error

    Keystone Industries is recalling 240 units of Henry Schein Hard Line Chairside Reline kits because the outer box is labeled as Soft Line, though the contents and instructions are correctly labeled.

    Product
    Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture Relining Material KI Item No.: 0921940HS Henry Schein Item No.: 570-0718
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V637000·2023-09-15

    Winnebago motorhomes recalled for incorrect hitch weight labels

    Winnebago is recalling multiple 2020-2022 motorhome models due to an incorrect hitch label that can lead to vehicle overloading. Dealers will install the correct label at no cost.

    Product
    WINNEBAGO — WINNEBAGO SPIRIT, VITA, VIEW, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-09132023-01·2023-09-13

    Kirkland Signature Chicken Tortilla Soup Recalled for Gluten Misbranding

    USDA FSIS issued a public health alert for Kirkland Signature Chicken Tortilla Soup labeled as gluten-free but containing gluten. No illnesses have been reported.

    Product
    Kettle Cuisine Midco, LLC — FSIS Issues Public Health Alert for Kirkland Signature Chicken Tortilla Soup Product Due to Misbranding
    Category
    Food
    Distribution
    8 states
  • HighNHTSA·23V633000·2023-09-13

    2023 Toyota Tundra Load Capacity Label Incorrectly States Weight Limit

    Toyota is recalling 2023 Tundra and Tundra Hybrid vehicles with spray-on bed liners due to an incorrect load carrying capacity label. The label overstates capacity, risking vehicle overload and crashes.

    Product
    TOYOTA — TOYOTA TUNDRA HYBRID, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1170-2023·2023-09-13

    Digoxin Tablets Recalled Due to Reversed Dosage Labeling

    Marlex Pharmaceuticals is recalling Digoxin Tablets because bottles labeled as 0.125mg contain 0.25mg strength, and vice versa. Approximately 94 100-count bottles distributed nationwide are affected.

    Product
    Digoxin Tablets, USP 0.25mg, 100-count bottles, Rx Only, Manufactured for/Distributed by: Marlex Pharmaceuticals, Inc. New Castle, DE NDC 10135-0748-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1146-2023·2023-09-13

    Prescription Dental Toothpaste Recalled Due to Incorrect Carton Labeling

    AvKARE is recalling Sodium Fluoride 1.1% prescription dental toothpaste because cartons are labeled as Capsaicin Cream 0.025%, though the tubes are correctly labeled. Approximately 35,184 tubes have been distributed to 19 consignees.

    Product
    SODIUM FLOURIDE — SODIUM FLOURIDE (SODIUM FLUORIDE)
    Category
    Drug
    Distribution
    0 states
  • SevereUSDA FSIS·043-2023·2023-09-09

    Custom Made Meals Recalls Bacon-Wrapped Chicken Products Due to Undeclared Milk Allergen

    Custom Made Meals, LLC is recalling approximately 1,345 pounds of bacon-wrapped chicken products because they contain undeclared milk, a known allergen.

    Product
    Custom Made Meals, LLC — Custom Made Meals, LLC Recalls Bacon Wrapped Chicken Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1488-2023·2023-09-06

    Mehlenbacher's Taffy strawberry lemonade recalled for undeclared milk allergen

    Mehlenbacher's Taffy strawberry lemonade is being recalled due to an undeclared milk allergen. Consumers with milk allergies are at risk.

    Product
    Mehlenbacher's Taffy, 1.25 oz per piece, 36 pieces/box, cello wrapped. Strawberry lemonade UPC 022099174035. Storage in a cool dry place.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1457-2023·2023-08-30

    Butter Flavored Popcorn recalled for undeclared milk

    Bickel's Snack Foods Inc is recalling Butter Flavored Popcorn because the product contains undeclared milk. The recall affects approximately 6,048 bags distributed in Georgia and nationwide retail stores.

    Product
    Butter Flavored Popcorn Naturally & Artificially Flavored, 8oz. UPC: 70175 06021 Packaged in clear plastic bags, 9 bags per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1455-2023·2023-08-30

    Lidl Blueberry Bagels Recalled for Undeclared Sesame Allergen

    Crispy Bagel Co. is recalling Blueberry Artificially Flavored Bagels sold at Lidl for containing undeclared sesame. Approximately 3,020 units were distributed to stores in Virginia, North Carolina, and Maryland.

    Product
    Blueberry Artificially Flavored Bagels By Lidl NET WT 20 OZ (1 LB 4 OZ) 567 g UPC: 2099 0305 Packaged in a plastic bag
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2443-2023·2023-08-30

    Femur nail surgical implant mislabeled with incorrect product length

    Smith & Nephew recalled a femur nail surgical implant because some packages contained a 40cm product instead of the labeled 36cm version. No injuries have been reported.

    Product
    TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT, REF 71647336, Femur nail
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-1458-2023·2023-08-30

    Doritos Nacho Cheese Tortilla Chips recalled due to undeclared soy and wheat

    Frito-Lay is recalling specific batches of Doritos Nacho Cheese Flavored Tortilla Chips because they may contain undeclared soy and wheat, which are major allergens.

    Product
    Doritos Nacho Cheese Flavored Tortilla Chips Party Size-14 1/2 oz. (411 g) Doritos Nacho Cheese Flavored Tortilla Chips, 1 oz.
    Category
    Food
    Distribution
    1 state