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.

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.

7001–7025 of 9611

  • ModerateFDA (Devices)·Z-0072-2015·2014-10-22

    Ameditech Recalls ArcPoint Labs 10 Panel Dip Screen Due to Labeling Error

    Ameditech is recalling 80 kits of ArcPoint Labs 10 Panel Dip Screen because the positive interpretation illustration on the cap labels and package insert was incorrect.

    Product
    ArcPoint Labs 10 Panel Dip Screen (BAR), Part No. APD-10M. The ArcPoint Labs Dip Drug Screen Dip Card is a one-step immunoassay for the qualitative detection of multiple drugs and drug metabolites in human urine.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Drugs)·D-0019-2015·2014-10-22

    Valeant Recalls Vasotec Tablets Due to Incorrect Package Insert Labeling

    Valeant Pharmaceuticals is recalling 205,853 bottles of Vasotec (enalapril maleate) tablets because they were packaged with the incorrect version of the package insert.

    Product
    VASOTEC — VASOTEC (ENALAPRIL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0076-2015·2014-10-22

    Arrow International Recalls Central Venous Catheter Kits Due to Labeling Error

    Arrow International is recalling 65 Multi-Lumen Central Venous Catheterization Kits because the outer shipping box displays an incorrect expiration date. The kits inside are correctly labeled and pose no risk to patients.

    Product
    Multi-Lumen Central Venous Catheterization Kit
    Category
    Medical Device
    Distribution
    10 states
  • LowFDA (Drugs)·D-0018-2015·2014-10-22

    Vaseretic Tablets Recalled for Incorrect Package Insert Version

    Valeant Pharmaceuticals is recalling Vaseretic tablets because they were packaged with the incorrect version of the package insert.

    Product
    VASERETIC — VASERETIC (ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·070-2014·2014-10-16

    Shop Packaging Recalls Chicken Wings for Undeclared Soy Allergen

    Shop Packaging LLC is recalling 115,505 pounds of chicken wings due to misbranding and an undeclared soy allergen. The products were shipped to New York.

    Product
    Shop Packaging, LLC — Massachusetts Firm Recalls Chicken Products Due to Possible Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0001-2015·2014-10-15

    Whole Foods 365 Mini Butter Croissants Recalled for Undeclared Egg Allergen

    Whole Foods Market is recalling 365 brand Mini Butter Croissants because they contain egg, which is not listed on the label.

    Product
    Mini Butter Croissant 6 Pack Ingredients: Wheat Flour (unbleached enriched wheat flour, malted barley flour, niacin, Iron, thiamin mononitrate, riboflavin, ascorbic acid, folic acid), Butter, Water, Sugar, Non Fat Dry Milk, Yeast, Salt, Dough Conditioner (dextrose, wheat flour,
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0018-2015·2014-10-15

    Cardinal Health Prefilled Buffered 10% Formalin Recalled for Concentration Issues

    Richard-Allan Scientific Company is recalling Cardinal Health Prefilled Buffered 10% Formalin because the formalin concentration may be outside specifications.

    Product
    Cardinal Health Prefilled Buffered 10% Formalin. Product Usage:10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0004-2015·2014-10-15

    Maruto C Wheat Cake Recalled for Missing Soy Allergen Labeling

    Ikko International Trading LLC is voluntarily recalling Maruto 'C' Wheat Cakes because the packaging omitted soy lecithin as an ingredient and allergen warning.

    Product
    Wheat Cake (Maruto "C" Cake), 6.3 ounces (180g), individually packaged in gold foil pouches and sold under the Maruto Brand. Sold at retail locations in display cases containing 8 bars per display case.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0015-2015·2014-10-15

    NatureBox Cranberry Macaroon Granola Recalled for Incorrect Back Label

    NatureBox is recalling 1,262 pouches of Cranberry Macaroon Granola because the back label incorrectly displays ingredients and nutrition for Cherry Berry Granola.

    Product
    naturebox cranberry macaroon granola net wt. 3.75 oz (106g) naturebox.com Back label incorrectly has nutrition and ingredients for cherry berry granola labeled in part as: Ingredients: Whole grain oats, brown sugar, dried cranberries (cranberries, sugar, sunflower oil) almo
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0017-2015·2014-10-15

    Richard-Allan Scientific Recalls Specimen Transportation System Due to Concentration Issues

    Richard-Allan Scientific is recalling 264 cases of its Specimen Transportation System because the NBF concentration may be outside specifications.

    Product
    Richard-Allan Scientific Specimen Transportation System. 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0014-2015·2014-10-15

    Richard-Allan Scientific Recalls 10% Neutral Buffered Formalin Due to Concentration Issues

    Richard-Allan Scientific is recalling 10% Neutral Buffered Formalin because the concentration may be outside specifications. The product is used to fixate tissue for histological examination.

    Product
    Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0016-2015·2014-10-15

    Richard-Allan Scientific Recalls 10% Neutral Buffered Formalin Due to Concentration Issues

    Richard-Allan Scientific is recalling 199 cases of 10% Neutral Buffered Formalin because the chemical concentration may be outside of desired specifications.

    Product
    Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0062-2015·2014-10-15

    Orthohelix MaxLock Reamer Recalled for Incorrect Laser-Etched Sizing

    Orthohelix Surgical Designs is recalling 38 MaxLock Extreme Mod-Foot Concave Reamers because incorrect sizing was laser-etched on the devices.

    Product
    MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat sealed with label on the outside. Used during procedures to clear away bone and cartilage within the desired implant area.
    Category
    Medical Device
    Distribution
    12 states
  • LowFDA (Devices)·Z-0015-2015·2014-10-15

    Richard-Allan Scientific Recalls Bio-Tite Specimen Containers Due to Concentration Issues

    Richard-Allan Scientific is recalling Bio-Tite Specimen Containers because the NBF concentration may be outside specifications.

    Product
    Richard-Allan Scientific Bio-Tite Specimen Containers. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0013-2015·2014-10-15

    Richard-Allan Scientific Recalls Specimen Transportation System Due to Concentration Issues

    Richard-Allan Scientific is recalling 285 cases of its Specimen Transportation System because the NBF concentrations may not meet specifications.

    Product
    Richard-Allan Scientific Specimen Transportation System. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0012-2015·2014-10-15

    Richard-Allan Scientific Recalls Protocol 10% NBF Tissue Fixative

    Richard-Allan Scientific is recalling 175 cases of Protocol 10% NBF tissue fixative because the concentration may be outside specifications.

    Product
    Protocol 10% NBF Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·069-2014·2014-10-14

    Italian Style Wedding Soup Recalled for Undeclared Soy and Egg Allergens

    Fresh Food Manufacturing is recalling 1,008 pounds of Italian Style Wedding Soup because the label failed to declare soy and egg allergens.

    Product
    Fresh Food Manufacturing Company — Pennsylvania Firm Recalls Italian Style Wedding Soup Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-2537-2014·2014-10-08

    Bar Harbor Jam Company Recalls Blueberry Muffin Mix for Wheat Labeling

    Bar Harbor Jam Company is recalling Maine Wild Blueberry Muffin Mix because the label does not declare wheat. The product was distributed in Maine, New Hampshire, and Massachusetts.

    Product
    BAR HARBOR JAM COMPANY Maine Wild Blueberry Muffin Mix; Net Wt. 1 lb 6 oz (624 g)
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2538-2014·2014-10-08

    Bar Harbor Jam Company Popover Mix Recalled for Undeclared Wheat

    Bar Harbor Jam Company is recalling Maine Old Fashioned Popover Mix because the label does not declare wheat. The product was distributed in Maine, New Hampshire, and Massachusetts.

    Product
    BAR HARBOR JAM COMPANY Maine Old Fashioned Popover Mix; Net Wt 1 lb 5 oz (624g)
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2536-2014·2014-10-08

    Bar Harbor Jam Company Recalls Blueberry Pancake Mix for Wheat Mislabeling

    Bar Harbor Jam Company is recalling Maine Wild Blueberry Pancake Mix because the label fails to declare wheat, posing a risk to individuals with wheat allergies.

    Product
    BAR HARBOR JAM COMPANY Maine Wild Blueberry Pancake Mix; Net Wt. 1 lb 6 oz (624 g)
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0005-2015·2014-10-08

    Siemens Medical Imaging Systems Recalled for Image Loss and Labeling Errors

    Siemens is recalling five Luminos Agile Max systems due to malfunctions that cause image loss and incorrect labels, leading to repeated examinations.

    Product
    Siemens Luminos Agile Max system The Luminos Agile is intended to be used as a universal imaging system for radiographic and fluoroscopic studies. Using either film cassettes or a digital mobile flat detector, it can perform a range of applications including general R/F, angiog
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2725-2014·2014-10-08

    Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions

    Instrumed International is recalling 83 reusable laparoscopic instruments to add caution statements regarding voltage limits and product useful life.

    Product
    Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for manip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2723-2014·2014-10-08

    Instrumed Reusable Laparoscopic Instruments Recalled for Updated Caution Statements

    Instrumed International is recalling 156 reusable laparoscopic instruments to add caution statements regarding voltage limits and useful life to the Instructions For Use.

    Product
    Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for manip
    Category
    Medical Device
    Distribution
    Distributed nationwide