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.

101–125 of 9606

  • HighFDA (Devices)·Z-1939-2026·2026-04-29

    Diversatek Healthcare Viper Balloon Dilator catheter inflation tag error

    Diversatek Healthcare is recalling Viper 3-Stage Wire Guided Balloon Dilators because the catheter inflation tag may contain an incorrect part number with wrong balloon diameter sizes and inflation pressures.

    Product
    Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 12mm-13.5mm-15mm, REF 1205-15
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Devices)·Z-1941-2026·2026-04-29

    Diversatek Viper Wire Guided Balloon Dilator Inflation Tag Incorrect

    Diversatek Healthcare is recalling Viper 3-Stage Wire Guided Balloon Dilators because the attached inflation tag may contain an incorrect part number with wrong balloon diameter sizes and inflation pressures.

    Product
    Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 18mm-19mm-20mm, REF 1205-20
    Category
    Medical Device
    Distribution
    19 states
  • LowFDA (Drugs)·D-0490-2026·2026-04-29

    Monsel's Solution ferric subsulfate vials recalled for incorrect expiration date printing

    Premier Dental Products is recalling Monsel's Solution (ferric subsulfate) 8 mL vials because the expiration date on the vial itself is printed with an extra digit (2709114 instead of 270914). The carton expiration date is correct.

    Product
    MONSELS SOLUTION — MONSELS SOLUTION (FERRIC SUBSULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·26429·2026-04-23

    mGanna Sodium Hydroxide Pellet Bags Recalled Over Chemical Burn Risk

    mGanna sodium hydroxide pellet bags sold on Amazon by Archie Xpress are recalled because the packaging is not child-resistant, risking chemical burns to skin and eyes.

    Product
    mGanna Sodium Hydroxide (lye) Pellet Bags
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0650-2026·2026-04-15

    Zarlengo's Chocolate Chocolate Chip Gelato Recalled for Undeclared Soy Allergen

    Zarlengo Italian Ice is recalling Chocolate Chocolate Chip Gelato in multiple sizes because soy lecithin is listed in the ingredients but soy is not declared in the allergen statement, posing a risk to consumers with soy allergies.

    Product
    Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon bucket/pail and 2-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminat
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1775-2026·2026-04-15

    Cook Medical Micro Wire Guides Recalled Due to Incorrect Expiration Dates

    Cook Incorporated is recalling specific lots of COOK MEDICAL Approach CTO-6 Micro Wire Guides because they were labeled with expiration dates that exceed their actual shelf life.

    Product
    COOK MEDICAL Approach CTO-6 Micro Wire Guide, Reference Part Number CMW-14-190-6G, Order Number G50786
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0637-2026·2026-04-08

    Divided Sunset Multi Collagen Peptides Missing Allergen Labeling

    TG FOODS INC is recalling Divided Sunset Multi Collagen Peptides (8 oz) because the product contains eggshell membrane collagen and wild-caught marine collagen but fails to declare EGG and the specific fish species on the label.

    Product
    Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Pouch, UPC Code: 8 50005 60689 5
    Category
    Food
    Distribution
    28 states
  • ModerateNHTSA·26V221000·2026-04-08

    Forest River Recalls 2026 Travel Trailers Due to Incorrect Weight Labeling

    Forest River is recalling 2026 Westbrook and Avenger travel trailers because the Federal Placard label may list an incorrect dry weight, potentially leading to vehicle overloading.

    Product
    FOREST RIVER — FOREST RIVER AVENGER, WESTBROOK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0623-2026·2026-04-01

    Pan de Bono Cheese Bread Recalled for Undeclared Soy Allergen

    South Florida Food, LLC is recalling Pan de Bono (Cheese Bread) because the product contains undeclared soy, a common allergen that poses a health risk to consumers with soy allergies.

    Product
    Pan de Bono (Cheese Bread), 100 units per Paper Cardboard Box, Net Wt 14.4 lb. KEEP FROZEN
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0602-2026·2026-04-01

    Bulk Colustrum Powder Missing Milk Allergen Declaration

    Herbal Creations USA is recalling bulk packaged Colustrum Powder because the product label does not declare milk as an allergen ingredient, posing a risk to consumers with milk allergies.

    Product
    Bulk packaged Colustrum Powder. packaged with generic product label.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0649-2026·2026-04-01

    Doraditas de Azucar recalled due to missing allergen labeling

    Distribuidora de Alimentos Sendero LLC is recalling Doraditas de Azucar because the product label is missing declarations for wheat and soy allergens.

    Product
    Doraditas de Azucar UPC 5901234123457
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0631-2026·2026-04-01

    Favorina Chocolate Ladybugs Recalled for Undeclared Tree Nut

    Lidl US is recalling Favorina Chocolate Ladybugs German-Style Nougat because the label does not specify which tree nut is contained in the product, posing a risk to consumers with tree nut allergies.

    Product
    Favorina Chocolate Ladybugs German-Style Nougat, Net Wt 3.52 oz (100g). UPC 2030 4492. Distributed By Lidl US, LLC, 3500 S. Clark St, Arlington, VA 22202. Product of Germany.
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·H-1108-2026·2026-03-25

    Shaman Botanicals Recalls White Vein Advanced Alkaloids Chewable Tablets

    Shaman Botanicals is recalling White Vein Advanced Alkaloids Chewable Tablets because the active ingredient quantity exceeds the labeled specification.

    Product
    Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 3
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0554-2026·2026-03-18

    Coco's Italian Market Cannoli Making Kit Missing Allergen Declarations

    Coco's Italian Market Cannoli Making Kit is recalled because the label lists flour and ricotta cheese as sub-ingredients but fails to declare wheat and milk allergens. Consumers with wheat or milk allergies may be at risk if they consume the product.

    Product
    Coco's Italian Market Cannoli Making Kit with 6 Cannoli Shells & Cream, Net Wt. 8 oz. (227g), Keep Frozen, packaged in a plastic container, UPC 0680334992716
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·H-0545-2026·2026-03-18

    C2O Coconut Water with Pulp 15-pack with incorrect outer box labels

    The outer cardboard box of C2O Coconut Water with Pulp (17.5 oz) 15-packs contains incorrect Nutrition Facts and Ingredient Lists that fail to disclose 5g of added sugar per can, although the can itself has correct labeling.

    Product
    C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8
    Category
    Food
    Distribution
    11 states
  • ModerateUSDA FSIS·PHA-03132026-01·2026-03-13

    Shaw Bakers Turkey Pesto Pastry Recall Due To Misbranding

    USDA FSIS issued a public health alert for Shaw Bakers turkey pastries that may contain ham and cheese instead of turkey.

    Product
    Shaw Bakers LLC — FSIS Issues Public Health Alert For Frozen Ready-To-Eat Turkey Stuffed Pastry Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0574-2026·2026-03-11

    Karns Foods Mini Dark Chocolate Raspberry Cups recalled for undeclared peanuts

    Karns Prime And Fancy Foods is recalling Mini Dark Chocolate Raspberry Cups because they may contain undeclared peanuts. The product was distributed only in Pennsylvania.

    Product
    Karns Foods, Mini Dark Chocolate Raspberry Cups, 8 oz Clear plastic tamper evident packs, 36-42 packed per breakout
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1459-2026·2026-03-04

    Knee and Humeral Socket Implants Recalled for Incorrect Labeling

    Encore Medical, LP is recalling 14 EMPOWR 3D KNEE implants because they contain incorrect labeling. The recall affects US nationwide distribution.

    Product
    Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1460-2026·2026-03-04

    Reverse Shoulder Prosthesis Implants Recalled Over Incorrect Labeling

    Encore Medical, LP is recalling 20 Reverse Shoulder Prosthesis implants due to incorrect labeling. The recall affects nationwide distribution across multiple US states.

    Product
    Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/Catalog Number: 509-00-036
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0532-2026·2026-03-04

    Frozen Fish Balls Recalled Due to Undeclared Wheat and Sesame

    Min Jiang Food Store Inc is recalling frozen fish balls because they contain undeclared wheat and sesame, which are common allergens.

    Product
    Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 810093891320
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·H-0528-2026·2026-03-04

    FDA Recalls Yoyo Gummy Tropical Flavor Candy for Unauthorized Color Additive

    SB FOOD LLC is recalling Yoyo Gummy Tropical Flavor candy because it contains Carmoisine (E122), a color additive not approved for use in this product. The recalled product was distributed to 15 states.

    Product
    Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
    Category
    Food
    Distribution
    15 states