The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 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.

4751–4775 of 9607

  • ModerateFDA (Devices)·Z-1782-2017·2017-04-19

    GE Healthcare Recalls Centricity PACS Web Diagnostic Software

    GE Healthcare is recalling 118 units of Centricity PACS Web Diagnostic software due to a defect where study category labels and hanging positions appear incorrectly swapped.

    Product
    Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various imaging sources within the system or across computer networks at distributed locations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1803-2017·2017-04-19

    FDA Recalls 2k Innovations Heated Lower Back Garment for Unapproved Claims

    2k Innovations Inc. is recalling 22,757 Volt Resistance Heated Lower Back Garments because FDA inspections found the firm made unapproved therapy and medical claims on product information and its website.

    Product
    Volt Resistance Heated Lower Back Garment Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1802-2017·2017-04-19

    2k Innovations Recalls Heated Neck Garments for Unapproved Medical Claims

    2k Innovations Inc. is recalling 22,757 Volt Resistance Heated Neck Garments because FDA inspections found the firm made unapproved therapy and medical claims on product information and its website.

    Product
    Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1805-2017·2017-04-19

    Volt Resistance Heated Therapy Foot Wrap Recalled for Unapproved Medical Claims

    2k Innovations Inc. is recalling 22,757 Volt Resistance Heated Therapy Foot Wraps because FDA inspections found unapproved therapy and medical claims on product information and the company website.

    Product
    Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1812-2017·2017-04-19

    FDA Recalls Volt Heated Slippers for Unapproved Medical Claims

    2k Innovations Inc. is recalling Volt Resistance Heated Slippers because the firm made unapproved therapy and medical claims on product information and its website.

    Product
    Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1804-2017·2017-04-19

    2k Innovations Recalls Volt Resistance Heated Therapy Shoulder Wrap

    2k Innovations Inc. is recalling 22,757 Volt Resistance Heated Therapy Shoulder Wraps because the firm made unapproved therapy and medical claims on product information and its website.

    Product
    Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1900-2017·2017-04-19

    Good Plenty Supreme Abalone Noodles Recalled for Undeclared Wheat

    Lian Hwa Foods is recalling Good Plenty Supreme Abalone Noodles because wheat was not properly declared on the label.

    Product
    Good Plenty Brand Supreme Abalone Noodles, 21.2 oz. box. Each box contains Retort pouch of Noodles and Abalone. These two pouches are packed together in the box; 10 boxes per case.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1960-2017·2017-04-19

    Classik Foods Recalls Maggi 2 Minute Noodles for Misbranding

    Classik Foods Inc. is voluntarily recalling Maggi 2 Minute Noodles in Florida and Georgia due to misbranding. No illnesses have been reported.

    Product
    Maggi 2 Minute Noodles, Net Wt. 19.75 oz., 2.46 oz. and 9.87 oz.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1807-2017·2017-04-19

    2k Innovations Recalls Volt Heated Elbow Garments for Unapproved Claims

    2k Innovations is recalling 22,757 Volt Resistance Heated Elbow Garments because FDA inspections found the firm made unapproved therapy and medical claims.

    Product
    Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1818-2017·2017-04-19

    Keystone Dental Recalls PrimaConnex Straight Implants Due to Mislabeling

    Keystone Dental Inc. is recalling 59 PrimaConnex Straight Implants because they were incorrectly labeled as Tapered Implants.

    Product
    Keystone Dental Inc. PrimaConnex Straight Implant TC, WD Internal Connection 5.0 x 11.5mm. Catalog Number(s): 15636K
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-1809-2017·2017-04-19

    2k Innovations Recalls Volt Heated Socks for Unapproved Medical Claims

    2k Innovations is recalling Volt Resistance Heated Socks because FDA inspections found the product makes unapproved therapy and medical claims.

    Product
    Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1813-2017·2017-04-19

    FDA Recalls Heated Slippers for Unapproved Medical Claims

    2k Innovations Inc. is recalling Volt Resistance Unisex Rechargeable Heated Slippers because FDA inspections found the company made unapproved therapy and medical claims.

    Product
    Volt Resistance Unisex Rechargeable Heated Slipper (All sizes) Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1767-2017·2017-04-19

    Smiths Medical CADD Administration Set Recalled for Incorrect Filter Size Illustration

    Smiths Medical is recalling CADD Administration Sets because the illustration on the Instructions for Use incorrectly depicts the filter size as 2.0 microns instead of the actual 0.2 microns.

    Product
    CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
    Category
    Medical Device
    Distribution
    43 states
  • HighNHTSA·17V258000·2017-04-18

    Volvo Recalls 2015-2017 VHD Trucks for Incorrect Axle Weight Labels

    Volvo is recalling 2015-2017 VHD trucks because the Gross Axle Weight Rating on the certification label may be incorrect, which could lead to vehicle overloading.

    Product
    VOLVO — VOLVO VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V256000·2017-04-18

    Honda Recalls 2017 CR-V and Acura RDX for Fading Certification Labels

    Honda is recalling 2017 CR-V and Acura RDX vehicles because certification labels may wipe away with alcohol solvents, potentially leading to vehicle overload.

    Product
    ACURA — ACURA, HONDA RDX, CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1878-2017·2017-04-12

    IKEA Recalls Chocolate Products for Undeclared Milk, Almond, and Hazelnut Allergens

    IKEA is recalling specific chocolate products due to undeclared milk, almond, and hazelnut allergens. Consumers with allergies should not consume these items.

    Product
    Choklad Not; Milk Chocolate with hazelnut Net Wt 3.5 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-1861-2017·2017-04-12

    Amish Bakery Chocolate Chip Bar Recalled for Missing Soy Label

    Original Amish Bakery LLC is recalling Chocolate Chip Grand-ola Bars because the label failed to list soy as an ingredient.

    Product
    Schlabach Amish Bakery Chocolate Chip Grand-ola Bar NET WT. 2.8 OZ (80g) UPC 0 14757 13000 2 Contains: Wheat, Tree Nuts, Dairy Ingredients: Oats, chocolate chips (sugar,chocolate liquor, cocoa butter, whole milk, lecithin [an emulsifier], salt, vanilla), brown sugar, wheat, corn
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1826-2017·2017-04-12

    Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars Recalled for Almond Mislabeling

    Nestle USA is recalling Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars because two consumers found almond bars in the packaging. The product was distributed in eight states and Washington, D.C.

    Product
    Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars; 3 - 3 FL oz.. bars (9 FL ox (266 ml)
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-1876-2017·2017-04-12

    IKEA Recalls Chocolate Wafers for Undeclared Hazelnut and Almond

    IKEA is recalling Godis Chokladran chocolate wafers because the packaging fails to declare hazelnut and almond ingredients, posing a risk to consumers with allergies.

    Product
    Godis Chokladran Wafers filled and covered with Milk chocolate; Net Wt 5.9 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-1837-2017·2017-04-12

    Kwei Chow Mustard Strip Recalled for Undeclared Wheat Allergen

    Kwei Chow Sauce Industry Co., Ltd. is recalling 8,488 jars of Mustard Strip with chili in oil because the product contains undeclared wheat.

    Product
    Kwei Chow brand Mustard Strip with chili in oil, net weight 7.05 Oz, sauce in glass jars, shelf stable
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1873-2017·2017-04-12

    IKEA Recalls Dark Chocolate Bars for Undeclared Milk, Almond, and Hazelnut

    IKEA is recalling specific dark chocolate bars because they contain undeclared milk, almond, and hazelnut. Consumers with allergies to these ingredients should not eat the product.

    Product
    Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.5 OZ. AND Chokland Mork Dark Chocolate 70%, Net Wt. 3.5 OZ. Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-1862-2017·2017-04-12

    McShare's Nutritional Premix Recalled for Undeclared Soy Ingredient

    McShare's Inc is recalling iXL Advanced Performance Matrix Nutritional Premix because it contains low levels of undeclared soy.

    Product
    iXL Advanced Performance Matrix, Nutritional Premix, Net Wt. 50 lbs., Item No. 136375.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1863-2017·2017-04-12

    McShare's Inc Recalls Premix Premix Due to Undeclared Soy

    McShare's Inc is recalling 700 lbs of Premack HS Vitamin RDA Premix because it contains low levels of undeclared soy.

    Product
    Premark HS Vitamin RDA Premix, Net Wt. 50 lbs., Item No. 136375.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1724-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Italian SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1719-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits Due to Instruction Errors

    Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi French SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿
    Category
    Medical Device
    Distribution
    Distributed nationwide