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.

1426–1450 of 9607

  • SevereFDA (Devices)·Z-1833-2021·2021-06-16

    DeRoyal Heart Cath Procedure Packs Recalled for Anesthetic Mislabeling

    DeRoyal Industries is recalling 66 heart catheterization procedure packs due to mislabeling of anesthetic contents. The packs contain 0.5% Bupivacaine but are labeled as containing 1% Lidocaine, creating a medication error risk during surgery.

    Product
    DeRoyal Heart Cath Procedure Pack, REF 89-6556.08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0663-2021·2021-06-16

    Adobo para Chorizo Seasoning Recalled for Undeclared Soy Lecithin

    Jesmar Spices, LLC is recalling Adobo para Chorizo Seasoning for Sausage because it contains undeclared soy lecithin from chocolate used in the product. The allergen is not listed on the product label.

    Product
    Adobo para Chorizo - Chorizo Marinade - Seasoning for Sausage. Product is packaged in a plastic bucket seal with lid, 5 gallons. No UPC. The label is read in parts: "*** Adobo para Chorizo *** Seasoning for Sausage *** Ingredients: Dried Chilies, vinegar, almonds, salt, pepper,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0747-2021·2021-06-16

    365 Everyday Value Whey Protein Powder Mislabeled with Soy Protein

    365 Everyday Value Whey Protein Powder was mistakenly packaged with Soy Protein Powder. The affected canisters were distributed nationwide and may pose a risk to consumers with soy allergies.

    Product
    365 Everyday Value Whey Protein Powder Natural Vanilla Flavor, Net Wt. 13.9 oz. canisters, UPC 9948228764, Whole Foods Market 550 Bowie Street Austin, TX 78703. Store in a cool, dry place.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0678-2021·2021-06-16

    Kroger Chicken Street Taco Kit Recalled for Undeclared Egg Allergen

    The Kroger Co. is recalling Chicken Street Taco kits because the Chipotle Crema component contains egg, which is not declared on the product label. This poses a risk to consumers with egg allergies.

    Product
    Chicken Street Taco kit in a plastic tray with a clear plastic lid.
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-1845-2021·2021-06-16

    DePuy Synthes Hip Prosthesis Recall Due to Incorrect Size Labeling

    DePuy Orthopaedics recalled 50 hip prostheses with incorrect part numbers and sizes etched on the devices. The affected Lot D20111130 was distributed domestically and to Bermuda.

    Product
    DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number: 1365-21-000, Part Description: ARTICUL/EZE BALL 32 +1 GR
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Drugs)·D-0630-2021·2021-06-16

    Levetiracetam Tablets 250 mg Recalled for Incorrect Barcode

    McKesson Corporation is recalling Levetiracetam Tablets USP 250 mg due to a barcode error that could cause some units to be misread as Naproxen 500 mg, although the product label itself is correct.

    Product
    Levetiracetam Tablets USP, 250 mg UD 100 Tablets (10x10) boxes, Rx Only, Distributed By: McKesson Corporation 4971 Southridge Blvd., Suite 101 Memphis, TN 38141 Manufactured by: Aurobindo Pharma Limited Hyderabad-500 090, India NDC 63739-795-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0662-2021·2021-06-16

    Glaceau Vitaminwater XXX mislabeled; may contain sugar instead of zero sugar

    The Coca-Cola Company is recalling Glaceau Vitaminwater XXX acai-blueberry-pomegranate labeled as zero sugar because an incorrect label was used and the product may actually contain sugar.

    Product
    Glaceau Vitaminwater XXX labeled to be Glaceau Vitaminwater Zero Sugar XXX acai-blueberry-pomegranate, 16.9 FL OZ, made for glaceau, Atlanta, GA
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-1830-2021·2021-06-16

    VIA Microcatheter shipped with incorrect international labeling instead of US labels

    MICROVENTION INC. is recalling VIA Microcatheter units that were inadvertently shipped with international labeling instead of US-cleared labeling. Units were distributed in six U.S. states.

    Product
    VIA Microcatheter VIA 27 REF VIA-27-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1829-2021·2021-06-16

    VIA Microcatheter VIA 21 Recalled for International Labeling Error

    MICROVENTION INC. is recalling VIA Microcatheter VIA 21 units (Lot 19110403M) because they were shipped with international labeling instead of FDA-cleared US labeling.

    Product
    VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0661-2021·2021-06-16

    Mideo's Marinara Glass Jars Recalled for Incorrect Potassium Labeling

    RC Industries Inc. is recalling Mideo's Marinara Glass 32oz jars because the potassium content listed on the label does not match the actual amount per serving.

    Product
    Mideo's Marinara Glass 32oz jars - 6 jars per case
    Category
    Food
    Distribution
    9 states
  • LowFDA (Devices)·Z-1828-2021·2021-06-16

    VIA Microcatheter recalled due to incorrect international labeling shipped to US

    MicroVention is recalling certain VIA Microcatheter units that were shipped with international labeling instead of US-approved labeling. Affected units were distributed across six US states.

    Product
    VIA Microcatheter VIA 17 REF VIA-17-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·21V448000·2021-06-14

    Utilimaster Velocity Recalled for Incorrect Seating Capacity Placard

    Shyft Group is recalling 2021 Utilimaster Velocity vehicles because the tire and loading placard incorrectly states a seating capacity of one instead of two.

    Product
    UTILIMASTER — UTILIMASTER VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0653-2021·2021-06-09

    Kumpunny's Lemon Sage Parmesan Cream Sauce Recalled for Undeclared Milk

    Kumpunny's LLC is recalling Lemon, Sage Parmesan & Romano Cream Sauce because the label does not declare milk, which is present in the product as heavy cream and butter.

    Product
    Lemon, Sage Parmesan & Romano Cream Sauce. The product is in a 12.6 oz. Mason glass jar, lid and ring, and tamper evident shrink wrapped. UPC 8 60001 31924 8. The label is read in parts: "*** LEMON SAGE PARMESAN & ROMANO CREAM SAUCE *** Ingredients: Heavy whipping cream, white
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1697-2021·2021-06-09

    K2M Cascadia lumbar implants recalled for mislabeled dimensions

    K2M, Inc. is recalling Cascadia AN Interbody Convex lumbar implants due to incorrect dimensions listed on product labels for specific lot numbers and device sizes.

    Product
    Cascadia AN Interbody Convex 10x28x14mm Catalog Number: 6101-2102814NC-G2 Lumbar implants are intervertebral body fusion devices indicated for use with autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft when used as anadjunct t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0655-2021·2021-06-09

    Chicken Street Taco Kits Recalled for Undeclared Egg Allergen

    Reser's Fine Foods is recalling Chicken Street Taco Kits because the Chipotle Crema component contains egg that is not declared on the label, posing a risk to consumers with egg allergies.

    Product
    ***Chicken Street Taco Kit with Trays, item # 13454.38080, Refrigerated product, 2/4.985 lbs. kits in each case. Distributed by Reser's Fine Foods, Topeka, KS. ***Homechef Chicken Street Taco Kit with Trays, item # 40134.30435, Refrigerated product, 2/4.985 lbs. kits in each
    Category
    Food
    Distribution
    24 states
  • LowFDA (Drugs)·D-0601-2021·2021-06-09

    Thiamine HCl Injection Recall: Vials with Incorrect Lot Numbers

    Mylan Institutional LLC is recalling Thiamine Hydrochloride Injection USP 200 mg/2 mL due to vials labeled with incorrect lot numbers. The cartons contain the correct lot number 200906 but vials inside are labeled with lot number 200901.

    Product
    THIAMINE HYDROCHLORIDE — THIAMINE HYDROCHLORIDE (THIAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0624-2021·2021-06-02

    American Pop Corn Recalls Buttered Microwave Popcorn for Undeclared Milk Allergen

    American Pop Corn Co. is recalling buttered microwave popcorn bags packaged in boxes that fail to declare the major food allergen milk.

    Product
    Xtra Butter Microwave Popcorn bags packaged in cardboard boxes labeled to be Jolly Time Healthy Pop 100's Kettle Corn 100 Calorie Singles, 3 1.2 oz (34 g) Net Wt 4.8 oz (136 g), American Pop Corn Co. Sioux City, Iowa
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-0560-2021·2021-06-02

    Wild Rice Tomato Soup Recalled for Undeclared Wheat and Soy Allergens

    The Secret Garden of Park Rapids is recalling Wild Rice Tomato Soup because it contains undeclared wheat and soy allergens.

    Product
    Wild Rice Tomato Soup, UPC 91675-31004, The Secret Garden, Park Rapids, MN 56470
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-0598-2021·2021-06-02

    Native Fluoride Toothpaste Recalled for Incorrect Fluoride-Free Labeling

    Accupac, Inc. is recalling Native Fluoride Toothpaste for Sensitive Teeth because the primary label may incorrectly state 'Fluoride-Free' instead of 'With Fluoride.'

    Product
    Native Fluoride Toothpaste for Sensitive Teeth, with Fluoride, 5% potassium nitrate, 0.243% sodium fluoride (0.14% w/v fluoride ion), Net Wt. 4.1 oz.,116 g, , Distr by Native, San Francisco, CA 94111 NDC: 69423-903-41, UPC 0 37000 28803 9
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1675-2021·2021-06-02

    Roche Recalls Iron Gen 2 Reagent Cassettes Due to Discrepant Results

    Roche Diagnostics is recalling 20,468 Iron Gen 2 reagent cassettes because they may produce discrepant elevated results on specific analyzers.

    Product
    IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for the quantitative determination of iron in human serum and plasma on Roche/Hitachi cobas c and cobas Integra systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1686-2021·2021-06-02

    CooperSurgical Recalls Incorrectly Packaged Ultem Koh Cup Vaginal Delineators

    CooperSurgical is recalling specific Koh Cup vaginal delineators that were incorrectly packaged with a 3.5cm cup instead of the required 3.0cm model.

    Product
    The Ultem Polymeric Resin Koh Cup is a non- sterile, reusable vaginal fornices delineator. It is made of medical grade plastics and not made with natural rubber latex. Model Number(s): KCP-30-2
    Category
    Medical Device
    Distribution
    3 states
  • LowFDA (Food)·F-0630-2021·2021-06-02

    Dole Peach Slices Recalled for Incorrect Labeling

    Dole is recalling 2,120 cases of Yellow cling Peach Slices because the lid label incorrectly identifies the contents as Mixed Fruit.

    Product
    Dole Yellow cling Peach Slices in 100% Fruit Juice. Snack & Store Fridge Pack. Net Wt 15 oz. (425g). UPC 38900-00642. Manufactured for Dole Packaged Foods, LLC, Westlake Village, CA 91361. Packed in Thailand.
    Category
    Food
    Distribution
    8 states
  • SevereUSDA FSIS·022-2021·2021-05-28

    King's Command Foods Recalls Meatballs and Pork Patties for Undeclared Allergens

    King's Command Foods is recalling approximately 20,025 pounds of meatballs and pork patties because they contain undeclared egg, milk, or wheat.

    Product
    King's Command Foods, LLC — King's Command Foods, LLC. Recalls Meat and Poultry Meatballs and Pork Pattie Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    10 states
  • HighCPSC·21750·2021-05-27

    Williams Advanced Materials Recalls Three Chemicals for Packaging and Labeling Violations

    Williams Advanced Materials & Chemicals is recalling sodium hydroxide, heptane, and naphtha because the packaging is not child-resistant and labels violate federal requirements.

    Product
    Williams Advanced Materials & Chemicals Recalls Three Chemical Products Due to Failure to Meet Child-Resistant Packaging Requirement and Violation of FHSA Labeling Requirement (Recall Alert)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0497-2021·2021-05-26

    A Life African Market Recalls Unlabeled Shrayy Chalk for Lead and Arsenic

    A Life African Market Corp is recalling 344 lbs of unlabeled Shrayy white chalk found to contain elevated levels of lead and arsenic. The product was distributed in New York, Delaware, Massachusetts, and Pennsylvania.

    Product
    Shrayy (white chalk) packaged in .68lb bags of synthetic plastic; no label on packaging
    Category
    Food
    Distribution
    4 states