The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 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 588 (6%) are Severe.

Which agencies issued them

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.

5576–5600 of 9610

  • HighFDA (Food)·F-1397-2016·2016-06-01

    Jacobsen Corn Seasoning Salt Recalled for Undeclared Milk Allergen

    Jacobsen Salt Co. is recalling Corn Seasoning Salt Blue Cheese and Herb because the label declares blue cheese but fails to declare milk.

    Product
    Corn Seasoning Salt Blue Cheese and Herb. Plastic bottles, 6 bottles per case. various sizes: Wt. 5.7 oz. The UPC is 8 14417 02089 2. Product is labeled in parts: "***CORN SEASONING SALT BLUE CHEESE & HERB***INGREDIENTS: BLUE CHEESE, JACOBSEN SEA SALT, OREGANO, THYME***Manuf
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1403-2016·2016-06-01

    Simply Delicious Recalls Lemon Poppyseed Oat Bars Due to Mispackaging

    Simply Delicious is recalling Lemon Poppyseed Oat Bars because they were mispackaged with Coconut bars. The recall covers 142 cases distributed nationwide.

    Product
    Bobo's Oat Bars, Gluten Free, Lemon Poppyseed, Net Weight 3 oz (85g), packaged in clear plastic, 12 bars per sleeve, also sold as individual units. Manufactured by Simply Delicious, Inc.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1708-2016·2016-06-01

    Stryker Recalls Mislabeled Reprocessed Diagnostic Electrophysiology Catheters

    Stryker Sustainability Solutions is recalling 18 reprocessed diagnostic electrophysiology catheters because they were mislabeled for size.

    Product
    Reprocessed Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters; Model #: 401450, 401877. Indicated for temporary intracardiac sensing, recording, stimulation, and electrophysiology mapping of cardiac structures.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1386-2016·2016-06-01

    Nubreed Nutrition Recalls Undisputed Dietary Supplement for Non-Compliant Ingredient

    Nubreed Nutrition is voluntarily recalling Undisputed dietary supplements because they contain Acacia rigidula, which does not meet the definition of a dietary ingredient.

    Product
    Undisputed , all lot codes, Flavors: Watermelon, 330 grams packed in 20oz HDPE White Plastic Container, The product was sold in white bottles with a white cap, containing forty (40) powder servings; 12 /case
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1388-2016·2016-06-01

    Nubreed Nutrition Recalls Undisputed Dietary Supplement for Non-Compliant Ingredient

    Nubreed Nutrition is voluntarily recalling Undisputed dietary supplements because they contain Acacia rigidula, an ingredient that does not meet FDA dietary ingredient definitions.

    Product
    Undisputed , all lot codes, Flavors: Juicy Pineapple, 330 grams packed in 20oz HDPE White Plastic Container, The product was sold in white bottles with a white cap, containing forty (40) powder servings; 12 /case
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1387-2016·2016-06-01

    Nubreed Nutrition Recalls Undisputed Dietary Supplement for Non-Compliant Ingredient

    Nubreed Nutrition is voluntarily recalling all lot codes of Undisputed dietary supplements because they contain Acacia rigidula, an ingredient that does not meet FDA dietary ingredient definitions.

    Product
    Undisputed , all lot codes, Flavors: Lemon Lime, 330 grams packed in 20oz HDPE White Plastic Container, The product was sold in white bottles with a white cap, containing forty (40) powder servings; 12 /case
    Category
    Food
    Distribution
    0 states
  • LowFDA (Devices)·Z-1830-2016·2016-06-01

    Roche Recalls Hungarian Instructions for cobas EGFR Mutation Test Kits

    Roche is recalling 8 kits of cobas EGFR Mutation Test v2 and cfDNA Sample Preparation due to errors in the Hungarian translated instructions for use.

    Product
    cobas¿ EGFR Mutation Test, v2 and cobas¿ cfDNA Sample Preparation Hungarian Translation Instructions for Use
    Category
    Medical Device
    Distribution
    0 states
  • LowUSDA FSIS·045-2016·2016-05-27

    Burger's Ozark Recalls Pulled Pork Due to Incorrect Back Label

    Burger's Ozark Country Cured Hams is recalling approximately 150 pounds of seasoned pulled pork products because the back of the package displays an incorrect label for a beef brisket product.

    Product
    Burger's Ozark Country Cured Hams, Inc. — Recall Notification Report 045-2016 (Pulled Pork Products)
    Category
    Food
    Distribution
    1 state
  • HighUSDA FSIS·044-2016·2016-05-26

    Taylor Farms Recalls Chicken Salads Due to Undeclared Allergens

    Taylor Farms Florida is recalling 151 pounds of Wawa Thai style chicken mango salad because the packaging contains undeclared wheat and sesame allergens.

    Product
    Taylor Farms Florida, Inc. — Taylor Farms Florida Inc. Recalls Salads Containing Chicken Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1699-2016·2016-05-25

    FDA Recalls Onset Mixing Pen Due to Missing Use Period Labeling

    Valeant Pharmaceuticals is recalling 7,716 Onset Mixing Pens because the labeling fails to state the 18-month optimal use period from the start of use.

    Product
    Orapharma (Onpharma) Onset Mixing Pen Rx only, Product/Part Number 1054-02. Manufactured for Onpharma Inc. Los Gratos, CA 95030 The Mixing Pen is used to dispense a solution from a standard 3 mL size cartridge into a second fluid container.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1362-2016·2016-05-25

    MegaFood Multi for Women 40+ Recalled for Missing Iron Warning

    FoodState, Inc. is recalling MegaFood Multi for Women 40+ multivitamin bottles because the labels lack the required iron warning statement and child-resistant cap.

    Product
    MegaFood Multi for Women 40+, Multivitamin & Mineral Dietary Supplement packaged in glass bottles UPC:5149410321 -Packaged 60 tablets; UPC:5149410322 -Packaged 120 tablets
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V332000·2016-05-20

    Heartland Recalls 2017 Trailers With Incorrect Tire Pressure Labels

    Heartland is recalling 618 model year 2017 Wilderness, North Trail, and Mallard trailers because certification labels contain incorrect tire pressure information.

    Product
    HEARTLAND — HEARTLAND NORTH TRAIL, WILDERNESS, MALLARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V328000·2016-05-19

    Ameritrans 285 Shuttle Buses Recalled for Inaccurate Weight Rating Labels

    Ameritrans is recalling 2012-2016 285 shuttle buses because certification labels may list an inaccurate gross vehicle weight rating, potentially affecting vehicle handling.

    Product
    AMERITRANS — AMERITRANS 285
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1044-2016·2016-05-18

    Meijer Frozen Butternut Squash Ravioli Recalled for Undeclared Cashew and Almond

    Bertagni 1882 is recalling Meijer frozen Butternut Squash Ravioli because the product may contain undeclared cashew and almond.

    Product
    Meijer frozen Butternut Squash Ravioli, product is packaged in a paper box, net weight 12 oz., UPC 760236398479
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-1641-2016·2016-05-18

    Biomerieux Recalls Vitek 2 Gram Positive Susceptibility Test Cards

    Biomerieux Inc is recalling Vitek 2 Gram Positive Susceptibility Test Cards because the product insert fails to identify a performance limitation related to EUCAST breakpoints for Teicoplanin.

    Product
    Vitek 2 Gram Positive Susceptibility Test Cards (AST-P640 REF 418579), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphy
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1326-2016·2016-05-18

    Granna's 808 French Toast Recalled for Whey Mislabeling

    Granna's LLC is recalling 808 French Toast, Diced Potatoes, and Mandarin Oranges because the label lists whey instead of milk.

    Product
    Granna's 808 French Toast, Diced Potatoes, Mandarin Oranges in three compartment black, plastic tray, stored frozen
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1639-2016·2016-05-18

    Biomerieux Recalls Vitek 2 Gram Positive Susceptibility Test Cards for Labeling Error

    Biomerieux Inc is recalling Vitek 2 Gram Positive Susceptibility Test Cards because the product insert fails to identify a performance limitation related to EUCAST breakpoints for Teicoplanin.

    Product
    Vitek 2 Gram Positive Susceptibility Test Cards (AST-P636 REF 417951), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylo
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1323-2016·2016-05-18

    Salsa Dianne Lemon Pesto Sauce Recalled for Undeclared Milk Allergen

    Salsa Dianne is recalling Lemon Pesto Sauce because the label declares parmesan cheese but fails to declare milk, a major allergen.

    Product
    Lemon Pesto Sauce, net wt. 4 oz. (113 g). Product is packaged in a round Styrofoam containers with translucent plastic lid. The UPC is 8 20103 77213 6. The product is labeled in parts: "***Lemon Pesto***INGREDIENTS: Olive Oil, Lemon, Almonds, Garlic, Parmesan cheese, Cilantr
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1322-2016·2016-05-18

    Salsa Dianne Recalls Classic Pesto Sauce for Undeclared Milk Allergen

    Salsa Dianne is recalling Classic Pesto Sauce (with a twist) because the label declares Parmesan cheese but fails to list milk as an ingredient.

    Product
    Classic Pesto Sauce (with a twist), net wt. 4 oz. (113 g). Product is packaged in a round Styrofoam containers with translucent plastic lid. The UPC is 8 20103 77214 3. The product is labeled in parts: "***Classic Pesto (with a twist)***INGREDIENTS: Olive Oil, Brazil nuts, Gar
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1650-2016·2016-05-18

    Neusoft NeuViz 64 CT Scanner Software Icon Mismatch Recall

    Neusoft Medical Systems is recalling seven NeuViz 64 CT scanners due to a software defect where side decubitus icons did not match the patient position description.

    Product
    NeuViz 64 Multi-Slice CT Scanner System (consist if two variants: NeuViz 64e, NeuViz 64i)
    Category
    Medical Device
    Distribution
    5 states
  • ModerateUSDA FSIS·041-2016·2016-05-18

    Aurnish Pork Dumplings Recalled for Undeclared MSG

    Aurnish Enterprises is recalling pork dumplings because they contain monosodium glutamate (MSG) that is not listed on the label.

    Product
    Recall Notification Report 041-2016 (Pork Dumpling Products)
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1646-2016·2016-05-18

    Biomerieux Vitek 2 Gram Positive Susceptibility Test Cards Recalled for Labeling Error

    Biomerieux Inc is recalling Vitek 2 Gram Positive Susceptibility Test Cards because the product insert fails to identify a performance limitation related to EUCAST breakpoints for Teicoplanin.

    Product
    Vitek 2 Gram Positive Susceptibility Test Cards (AST-P645 REF 419602), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylo
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-1643-2016·2016-05-18

    Biomerieux Vitek 2 Gram Positive Test Cards Recalled for Labeling Error

    Biomerieux is recalling Vitek 2 Gram Positive Susceptibility Test Cards because the product insert fails to identify a performance limitation related to EUCAST breakpoints for Teicoplanin.

    Product
    Vitek 2 Gram Positive Susceptibility Test Cards (AST-P642 REF 418604), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylo
    Category
    Medical Device
    Distribution
    0 states