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.

2726–2750 of 9607

  • ModerateFDA (Devices)·Z-1799-2019·2019-06-26

    Arrowg+ard Blue Advance JACC Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling Arrowg+ard Blue Advance JACC products due to an incorrect expiration date listed by Lidstock.

    Product
    Arrowg+ard Blue Advance JACC Product Code: CDC 42041 JX1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1392-2019·2019-06-26

    Akorn Recalls Myorisan Isotretinoin Capsules Due to Labeling Error

    Akorn Inc. is recalling 16,216 cartons of Myorisan isotretinoin capsules because secondary cartons incorrectly state 40 mg instead of 30 mg.

    Product
    Myorisan (isotretinoin capsules, USP), 40 mg, packaged in cartons of 30 Capsules containing 3 x 10 Prescription Packs, Rx Only, Distributed by: VersaPharm Inc. - An Akorn Company, Lake Forest, IL 60045, NDC 61748-304-13
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1802-2019·2019-06-26

    Arrow JACC Central Catheter Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 6 units of Arrow JACC Central Catheters because the expiration date is incorrect.

    Product
    Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central Catheter Product Code: CDC 42552 JX1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1815-2019·2019-06-26

    Arrow JACC Medical Device Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 3 units of Arrow JACC with Chloragard Technology due to an incorrect expiration date.

    Product
    Arrow¿ JACC with Chlorag+ard Technology Product Code:JR 42563 HPHNM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1804-2019·2019-06-26

    Arrow JACC Central Catheter Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 12 units of JACC central catheters because the expiration date printed on the packaging is incorrect.

    Product
    Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central Catheter Product Code: CDC 43063 JX1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1843-2019·2019-06-26

    Cytocell Aquarius D13S319 Probe Recalled for Package Insert Error

    Cytocell Ltd. is recalling Aquarius D13S319 Plus Deletion Probes because the chromomap on the package insert contains an error.

    Product
    Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb region including most of the DLEU2 gene, part of the DLEU1 gene and the D13S319 and D13S272 markers. The 13qter subtelomere specific probe, labelled in green
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1454-2019·2019-06-19

    Meiji Chocolate Wheat Snack Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Takenoko no Sato bars because they lack English labels for ingredients and allergens, including milk, soy, egg, and tree nuts.

    Product
    CHOCOLATE TAKENOKO NO SATO MEIJI (Chocolate wheat snack, 2.46 oz. Item number 65880 UPC 074410658809 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1445-2019·2019-06-19

    Cool Haus Dairy-Free Horchata Frozen Dessert Recalled for Undeclared Milk

    Cool Haus is recalling its Dairy-Free Horchata Frozen Dessert Sandwich because it contains undeclared milk, a major allergen.

    Product
    Cool Haus Awesome Dessert - Dairy Free Horchata Frozen Dessert Sandwich. Horchata Rice Milk & Cinnamon frozen dessert with Snickerdoodle Cookies 5.8 fl. oz. in film wrapper. 10 individual items per case. UPC: 851916003650 Product number: CoolV004 Ingredients: Snickerdoodle
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-1771-2019·2019-06-19

    Philips Patient Information Center iX Recall for Infusion Pump Data Accuracy

    Philips is recalling Patient Information Center iX software because infusion pump data may be recorded at 100 times the actual rate.

    Product
    Philips Patient Information Center iX configured with a regional setting which uses a comma for a decimal separator: 866389 Patient Information Center iX B.01 (or later); 866390 Patient Information Center iX B.01 upgrade (or later) Product Usage: The intended use of the I
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1450-2019·2019-06-19

    Meiji Black Chocolate Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Black Chocolate bars because they lack English labels for nutrition facts, ingredients, and allergens.

    Product
    CHOCOLATE BLACK CHOCOLATE MEIJI, 1.75 oz. Item number 69341 UPC 074410693411 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1451-2019·2019-06-19

    Meiji Chocolate Almond Bars Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Almond bars because they lack English labels for ingredients and allergens, including milk, soy, egg, and tree nuts.

    Product
    CHOCOLATE ALMOND CHOCOLATE MEIJI, 3.1 oz. Item number 64344 UPC 074410643447 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1449-2019·2019-06-19

    Meiji Chocolate Milk Chocolate Bars Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Milk Chocolate bars because they lack English labels for ingredients and allergens, including milk, soy, egg, and tree nuts.

    Product
    CHOCOLATE MILK CHOCOLATE MEIJI, 1.75 oz. Item number 70378 UPC 074410703783 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1455-2019·2019-06-19

    Meiji Chocolate Choco Baby Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Choco Baby bars because they lack English labels for nutrition facts, ingredients, and allergens.

    Product
    CHOCOLATE CHOCO BABY (S) MEIJI, 1.19 oz. Item number 70582 UPC 074410705824 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1767-2019·2019-06-19

    Luminex xTAG Gastrointestinal Pathogen Panel Recalled for Lower MS2 MFI Values

    Luminex Molecular Diagnostics is recalling 965 xTAG Gastrointestinal Pathogen Panel kits due to reports of lower MS2 MFI values.

    Product
    xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple viral, bacterial and parasitic nucleic acids in human stool specimens or human stool (GPP) Kit, IVD, REF I032C0316.
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Drugs)·D-1395-2019·2019-06-19

    Pecgen DMX Recalled for Incorrect Pediatric Dosage Labeling

    Novis PR, Inc. is recalling Pecgen DMX cough syrup because a typo on the label provides incorrect dosage instructions for children.

    Product
    PECGEN DMX — PECGEN DMX (DEXTROMETHORPHAN HBR, GUAIFENESIN)
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Food)·F-1456-2019·2019-06-19

    Laird Superfood Performance Mushrooms Recalled for Iron Labeling Error

    Laird Superfood is recalling Performance Mushrooms because the label incorrectly lists 14 mg of Iron instead of the actual 14 mcg.

    Product
    Performance Mushrooms product is dried mushroom blend of 4 different mushroom mycelial biomass powders cultured on certified organic oats, brand Laird Superfood, uses as Beverage Booster and Functional Fuel Supplement. Product is packaged in 3.17 oz (90 gram) stand up with zip
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1433-2019·2019-06-12

    Topnotch Foods Natural Bread Crumbs Recalled for Undeclared Milk

    Topnotch Foods Inc is recalling 2,000 lbs of Natural Bread Crumbs due to undeclared milk. The product was distributed in California.

    Product
    Topnotch Foods Natural Bread Crumbs: 50 lb. Net Wt. 22.68 kg. and 10 lbs. 4.54 Kg. Item number 10021: Vernon, CA Correct Ingredients: Enriched, Bleached & Unbleached, Wheat Flour, [Flour, Malted Barley Flour, Niacin, Reduced Iron, Thiamine Mononitrate, Riboflavin, Foli
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·068-2019·2019-06-12

    Greener Pastures Chicken Recalls Raw Whole Poultry Produced Without Inspection

    Pasture Raised Foods, LLC is recalling raw whole poultry produced without federal inspection. The products were shipped to locations in Texas.

    Product
    Pasture Raised Foods, LLC Recalls Raw Whole Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1436-2019·2019-06-12

    New Seasons Market Recalls Bacon Shallot Potato Salad for Undeclared Egg

    New Seasons Market LLC is recalling Bacon Shallot Potato Salad sold in Oregon due to undeclared egg. The product was sold from the deli case between May 16 and May 21, 2019.

    Product
    Bacon Shallot Potato Salad, internal item PLU code 52365, sold as bulk from the full service deli case per costumers order. The salad was packed into plastic deli containers. The label is read in parts: "*** Potatoes, red wine vinaigrette (Dijon mustard [water, mustard seed
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1437-2019·2019-06-12

    Icco Cheese Co Recalls Gia Russa Bread Crumbs for Undeclared Allergens

    Icco Cheese Co Inc is recalling Gia Russa Whole Grain Italian Unseasoned Bread Crumbs because the product contains undeclared walnuts and pecans.

    Product
    Gia Russa Whole Grain Italian Unseasoned Bread Crumbs in 10 Oz Paperboard Canisters
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1434-2019·2019-06-12

    Topnotch Foods Italian Bread Crumbs Recalled for Undeclared Soy Lecithin

    Topnotch Foods Inc. is recalling 10 lb. bags of Italian Bread Crumbs found to contain undeclared soy lecithin during a California Department of Public Health inspection.

    Product
    Topnotch Foods Italian Bread Crumbs: 10 lb. Net Wt.. 10 lbs. (4.54 Kg) Item number 10008: Vernon, CA 90058 Correct ingredients: CRUMBS: Enriched, Bleached & Unbleached Wheat Flour, [Flour, Malted Barley Flour, Niacin, Reduced Iron, Thiamine Mononitrate, Riboflavin, Foli
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1477-2019·2019-06-12

    Sassy Cow Creamery Recalls Ice Cream Due to Undeclared Pecan Allergen

    Sassy Cow Creamery is recalling Art Cream Gluten Free Cookies & Cream ice cream because it was packaged in a container labeled for a different flavor, creating an undeclared pecan allergen risk.

    Product
    Art Cream Gluten Free Cookies & Cream ice cream, one pint. UPC 57897-00803. Products have been manufactured on Shared Equipment that Processes Peanuts, Tree Nuts, Milk, Wheat and Soybean Products.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1482-2019·2019-06-12

    Young Ocean Seasoned Alaskan Pollock Roe Recalled for Undeclared Allergens

    Young Ocean is recalling Seasoned Alaskan Pollock Roe because the label fails to declare bonito and lactose (milk) as ingredients.

    Product
    Young Ocean brand Seasoned Alaskan Pollock Roe, frozen, wrapped in plastic liner and packed in styrofoam box, and finally packed in cardboard box. Net wt. per pack: 1 lb. Each cardboard box contains 20/1 lb. packs. The label is read in parts: "***Seasoned Alaskan Pollock Roe
    Category
    Food
    Distribution
    1 state