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.

1151–1175 of 9606

  • HighFDA (Devices)·Z-1011-2022·2022-05-04

    Smart Toe II Surgical Implant Recalled: Obscured Nickel Warning Label

    Stryker GmbH recalls 246 Smart Toe II orthopedic implants due to label obstruction that obscures the nickel-sensitivity contraindication, potentially allowing inappropriate use.

    Product
    Smart Toe II Intramedullary Arthrodesis Implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0787-2022·2022-05-04

    Cough Medicine Recall: Undeclared Alcohol in Wal-Tussin DM

    Wal-Tussin DM cough medicine is being recalled because the product contains alcohol that was not declared on the label. Approximately 40,000–50,000 bottles distributed in Illinois are affected.

    Product
    Wal-Tussin DM (dextromethorphan HBr/Guaifenesin), 12 FL OZ (354 mL) bottles, Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0324-28.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0999-2022·2022-04-20

    Giant Eagle Happy Face Cookies Recalled for Undeclared Milk Allergen

    Giant Eagle recalled Happy Face Cookies from two Ohio stores due to undeclared milk allergen. Consumers with milk allergies should not consume these products.

    Product
    Giant Eagle, Happy Face Cookie Single 25065900000
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0982-2022·2022-04-20

    Lipton Iced Tea Peach 24-pack recalled for incorrect zero-sugar labeling

    Pepsico is recalling 780 cases of Lipton Iced Tea Peach 24-packs in four states due to incorrect labeling. Individual bottles labeled as zero sugar contain regular sugar.

    Product
    Lipton Iced Tea Peach, 24 Pack retail unit, 24 - 16.9 FL OZ Bottles. UPC on retail 24 pack: 012000023118
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0992-2022·2022-04-20

    Tattooed Chef Plant-Based Sausage Breakfast Bowl Recalled for False Gluten-Free Claim

    Ittella International recalls Tattooed Chef Plant-Based Sausage Breakfast Bowls nationwide due to an incorrect gluten-free claim on the container lid. The product contains wheat flour, which is correctly listed in the ingredients and allergen statement.

    Product
    Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life Box Net wt. 40oz (1.13kg) UPC: 850015982569 Packed for: Tattooed Chef Paramount, CA 90723
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0926-2022·2022-04-20

    Philips Autoclavable Temperature Probes: Updated Cleaning Instructions

    Philips is updating instructions for cleaning and disinfecting reusable autoclavable temperature probes due to revisions needed in the disinfection process.

    Product
    The IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in the packaging for the following product model #s: 21075A, 21076A, 21078A, 989803162621, 989803162631, 989803162641.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22V266000·2022-04-19

    Triple E RV Recalls 2021-2022 Wonder W24RL for Incorrect Weight Decal

    Triple E Recreational Vehicles is recalling 2021-2022 Wonder W24RL models because an incorrect weight decal may lead to overloading the storage compartment.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0749-2022·2022-04-13

    Sucralfate Oral Suspension Recalled Due to Label Mix-Up

    DASH Pharmaceuticals is recalling Sucralfate Oral Suspension nationwide due to a labeling mix-up affecting approximately 45,940 unit dose cups.

    Product
    Sucralfate Oral Suspension, USP 1g/10mL, packaged in a) 40 case of 10 mL unit Dose Cups (NDC 69339-148-17) and b) 100 case of 10 mL Unit Dose Cups (NDC 69339-148-19) Rx Only, Dash Pharmaceuticals, Upper Saddle River, NJ 07458.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0751-2022·2022-04-13

    Oral antiseptic rinse recalled due to label mix-up and wrong barcode

    The Natural Dentist Healthy Breath Antiseptic Rinse (Cool Mint) is being recalled due to a label mix-up. The back label incorrectly states the active ingredient as Peppermint Oil and Sage Oil and displays the wrong UPC code.

    Product
    The Natural Dentist Healthy Breath Antiseptic Rinse, Cool Mint, 16.9 FL OZ (500 mL, Manufactured for Revive Personal Products Company, Madison, NJ 07940, UPC Code 714132000714.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0875-2022·2022-04-13

    Vena Cava Filter Sets Recalled for Instruction for Use Documentation Updates

    Cook Medical recalled 24,641 Gunther Tulip Vena Cava Filter Sets due to updates required in the Instruction for Use documentation covering device description, indications, contraindications, warnings, and precautions.

    Product
    Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Catalog Number/GPN: IGTCFS-65-1-FEM-TULIP G52917; IGTCFS-65-1-JUG-TULIP G52916; IGTCFS-65-1-UNI-TULIP G52918
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22738·2022-04-07

    biOrigins Sodium Hydroxide Products Recalled for Non-Child-Resistant Packaging

    CPSC recalls biOrigins sodium hydroxide products sold on Amazon from July 2020 through July 2021 due to non-child-resistant packaging and missing hazard label information. The product poses risk of chemical burns and skin/eye irritation to children.

    Product
    biOrigins Sodium Hydroxide Products
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0842-2022·2022-04-06

    Ceramic Hip Femoral Head Component May Not Match Package Label

    Howmedica Osteonics is recalling certain Biolox delta Ceramic V40 Femoral Head components because the actual size and offset may not match the package label. Patients with these implants should contact their surgeon.

    Product
    Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0817-2022·2022-03-30

    Codman Cranial Access Kits Recalled Due to Incorrect Expiration Dates on Labels

    Integra LifeSciences is recalling 1,161 Codman Cranial Access Kits due to incorrect expiration dates on the outer box labels. Using the product past its correct expiration date may cause pain, infection, or adverse tissue reaction.

    Product
    Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage procedures. Product umber: 826614
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03252022-01·2022-03-25

    Taylor Farms Recalls Chicken Meal Kits Due to Undeclared Allergens

    Taylor Farms New England Inc. issued a public health alert for ready-to-eat chicken breast meal kits that may contain undeclared wheat and soy.

    Product
    Taylor Farms New England Inc. — FSIS Issues Public Health Alert for Ready-to-Eat Chicken Meal Kits Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0865-2022·2022-03-23

    Frozen Breakfast Tarts Recalled Due to Undeclared Almonds

    Gourmet Kitchen, Inc. is recalling 43 boxes of Raw Buttermilk Breakfast Tarts due to undeclared almonds. Consumers allergic to almonds should not consume this product.

    Product
    14" Raw Buttermilk Breakfast Tart with Cranberries, Apples & Granola P2004 (9 Frozen Pancakes). Barcode: 0106915030162004992201921137
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-0874-2022·2022-03-23

    Bob Evan's Mashed Potatoes Recalled for Undeclared Wheat Allergen

    Bob Evan's Sour Cream & Chive Mashed Potatoes recalled due to incorrect packaging that failed to declare wheat allergen. Consumers with wheat allergies should not consume this product.

    Product
    Bob Evan's Sour Cream & Chive Mashed Potatoes 24oz plastic trays with clear film and sleeve over wrap sold as singles to consumers
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0886-2022·2022-03-23

    Stutzman Farms Organic All Purpose Flour Recalled for Undeclared Wheat Allergen

    Stutzman Farms is recalling its Organic All Purpose Flour sold in bulk due to undeclared wheat allergen. The flour was distributed across seven states and may affect individuals with wheat allergies.

    Product
    Stutzman Farms Organic All Purpose Flour sold in bulk
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0869-2022·2022-03-23

    Honey BBQ seasoning recalled due to undeclared wheat allergen

    PS Seasoning & Spices recalls Honey BBQ Snack seasoning (3,001 units) distributed to 28 states and Canada due to undeclared wheat. Consumers with wheat allergies should not use affected lots.

    Product
    Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456. 2. 685-B, Net Wt 5.25 lbs. (2.38kg). Part #020001457. Ingredients: Sugar, Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder, Dextrose
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-0788-2022·2022-03-23

    LYFO Disk Quality Control Product Recalled for Organism Mislabeling

    Microbiologics Inc recalls LYFO Disk lot 983-40-3 because it is labeled as Candida tropicalis but actually contains Yersinia enterocolitica. The mislabeling may cause laboratory quality control failures and delayed test results.

    Product
    LYFO Disk
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0805-2022·2022-03-23

    Calcium Alginate Wound Dressings Recalled for Incorrect Instructions

    CellEra LLC is recalling Vitale Silver calcium alginate dressings nationwide because packages contain incorrect Instructions for Use with language not approved by the FDA. The firm is providing replacement packages with corrected instructions.

    Product
    20548 Vitale Silver calcium Alginate Dressings 4x8, 5/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0803-2022·2022-03-23

    Medical device wound dressing recall for incorrect instructions

    CellEra LLC is recalling Vitale Silver calcium Alginate Dressings because product packages contain incorrect Instructions for Use with language beyond FDA 510(k) clearance scope. The firm is replacing affected units with correct instructions.

    Product
    20544 Vitale Silver calcium Alginate Dressings 4x4, 10/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0854-2022·2022-03-16

    Coca-Cola Cherry Zero Sugar Recalls Cans Missing PKU Warning Label

    Coca-Cola Cherry Zero Sugar 12-packs distributed in AZ, UT, and WY are being recalled because individual cans lack required phenylketonuric (PKU) warning labels, which are necessary for people with phenylketonuria.

    Product
    Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12-pack fridge pack carton. UPC 049000047516; UPC Cherry Coca-Cola Zero Sugar can 049000047561; Cherry Coca-Cola can 04905004. There are 2 12-packs per case.
    Category
    Food
    Distribution
    3 states