The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (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.

5801–5825 of 9610

  • ModerateFDA (Devices)·Z-1247-2016·2016-03-30

    Neurotherm Curved Radiofrequency Cannula Recalled for Mislabeling

    Neurotherm, Inc. is recalling 135 curved radiofrequency cannulas because straight needles were incorrectly labeled as curved.

    Product
    Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip Model Number: C-1010-R-18 Product Usage: The device is a radiofrequency needle, used for the application of radiofrequency energy with as intended result, thermo coagulation of nervous tissue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1237-2016·2016-03-30

    Cook Medical Recalls Nephrostomy Balloon Sets Due to Labeling Mix-up

    Cook Medical is voluntarily recalling specific lots of Ultraxx Nephrostomy Balloon Sets and Ascend AQ Ureteral Dilation Balloon Catheter Sets because of a labeling mix-up.

    Product
    UltraxxTM Nephrostomy Balloon Set The Ultraxx" Nephrostomy Balloon Set consists of a radiopaque balloon catheter, radiopaque sheath, and inflation device. The Ultraxx" Nephrostomy Balloon Set is used to dilate the musculofascia, renal capsule, and parenchyma to establish and mai
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1238-2016·2016-03-30

    Cook Medical Recalls Ureteral Balloon Catheters Due to Labeling Mix-Up

    Cook Medical is voluntarily recalling specific lots of Ascend AQ Ureteral Dilation Balloon Catheter Sets and Ultraxx Nephrostomy Balloon Sets due to a labeling error where packages may contain the wrong product.

    Product
    Ascend¿ AQ¿ Ureteral Dilation Balloon Catheter Set The Ascend¿ AQ¿ Ureteral Dilation Balloon Catheter Set consists of a radiopaque balloon catheter and inflation device. The Ascend¿ AQ¿ Ureteral Dilation Balloon Catheter Set is used for transluminal dilation of ureteral strictur
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1235-2016·2016-03-30

    AcuFocus Recalls KAMRA Corneal Inlays Due to Shelf Life Labeling Concerns

    AcuFocus is recalling 182 KAMRA ACI 7000 Corneal Inlays because of concerns regarding the labeled shelf life. The devices were distributed in Canada, Germany, Saudi Arabia, Turkey, and the United Kingdom.

    Product
    KAMRA Inlay, ACI 7000 Corneal Inlay, Part No. 76195-01 and 76195-10 (OUS) Labeling: The KAMRA inlay is indicated for the improvement of near visual acuity in one eye (usually the non-dominant eye) of a presbyopic patient.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0774-2016·2016-03-30

    King Henry's Recalls Fruit and Nut Medley for Undeclared Dye

    King Henry's, Inc. is recalling Fruit & Nut Medley because it may contain undeclared FD&C Yellow #6. The recall covers 3,242 units distributed across 25 US states and British Columbia.

    Product
    Fruit & Nut Medley, Snacks Fit for a King, King Size, 12 per case. NP- UPC 61054645419 and 61054645119.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-0749-2016·2016-03-23

    Dawn's Potato Salad Recalled for Undeclared Milk, Wheat, and Soy Allergens

    Dawn's Foods is recalling Deluxe and Deviled Egg Potato Salads due to mislabeling and potential undeclared milk, wheat, and soy allergens.

    Product
    Dawn's Deviled Egg Potato Salad, Net Wt. 15 oz. (397g), UPC 32345-10107. Keep Refrigerated.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0756-2016·2016-03-23

    NatureBox Cinnamon Yogurt Mini Grahams Recalled for Allergen Mislabeling

    NatureBox is recalling Cinnamon Yogurt Mini Grahams because some bags were packaged in Probiotic Power Mix bags that fail to declare wheat as an allergen.

    Product
    NatureBox Cinnamon Yogurt Mini Grahams, 6 oz. (170g) customer stand up pouches. UPC 8 58590 00528 4 Ingredients: Graham Crackers (unbleached unenriched wheat flour, whole wheat graham flour, sugar, palm and palm kernel oil, molasses, honey, salt, sodium bicarbonate). Yogurt
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0750-2016·2016-03-23

    Dawn's Potato Salad Recalled for Undeclared Allergens

    Dawn's Foods is recalling Deluxe and Deviled Egg Potato Salad due to mislabeling and potential undeclared milk, wheat, and soy.

    Product
    Dawn's Deluxe Potato Salad, Net Wt. 15 oz. (425g), UPC 32345-10015. Keep Refrigerated.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0751-2016·2016-03-23

    Casper's Sea Salt Caramel Pretzel Ice Cream Recalled for Allergen Mislabeling

    Casper's Ice Cream is recalling Sea Salt Caramel Pretzel Ice Cream because it contains Caramel Cashew ice cream, presenting a potential allergen threat.

    Product
    Sea Salt Caramel Pretzel Ice Cream, Red Button Vintage Creamery, 56 fluid ounce, Paper Tub, 6 tubs per case, Distributed by Associated Foods, Inc. Utah; Manufactured by Caspers Ice Cream, Inc. Utah
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-0746-2016·2016-03-23

    Coca-Cola Recalls Mello Yello Cans for Undeclared Aspartame

    The Coca-Cola Company is recalling 2,522 cases of Mello Yello soda in Illinois, Indiana, and Ohio due to undeclared aspartame.

    Product
    Citrus Flavored Soda Mello Yello, 12 fl. oz. (355 ml), Canned under authority of The Coca-Cola Company, Atlanta, GA 30313, UPC 497250
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1180-2016·2016-03-23

    Steris Quick Connects Recalled Due to Hysteroscope Port Mismatch

    Steris Corporation is recalling 809 Quick Connect flow units because processing instructions incorrectly list a hysteroscope model with two inlet ports when the device has only one.

    Product
    Quick Connects. Steris Corporation. Model numbers: QKC1736E, QKC1736INT, QKC1737E, and QKC1737INT. Each Quick Connect contains a flow unit consisting of tubing, tethers, and adapters. For sterilant and rinse water used in endoscope washers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0773-2016·2016-03-23

    Teva Recalls Nabumetone Tablets Due to Missing Labels and Leaflets

    Teva Pharmaceuticals USA is recalling 576 bottles of Nabumetone 750 mg tablets because they lack required leaflets and approved labels.

    Product
    NABUMETONE Tablets USP, 750 mg, 100 count bottle,Teva Pharmaceutical Industries Ltd., Jerusalem, 91010, ISRAEL
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0775-2016·2016-03-23

    Virt-Nate Prenatal Supplement Recalled for Incorrect Tablet Imprinting

    Virtus Pharmaceuticals is recalling Virt-Nate Prenatal/Postnatal supplements because some bottles contain tablets with the wrong identification code.

    Product
    Virt-Nate Prenatal/Postnatal, Prescription Folate-Containing Dietary Supplement, Rx, 100 count bottles, Manufactured For: Virtus Pharmaceuticals, Tampa, FL
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Devices)·Z-1177-2016·2016-03-23

    Volk Optical Recalls G-4 Gonio Lenses Due to Incorrect Lot Number

    Volk Optical Inc is recalling G-4 Small Ring Gonio Lenses because the incorrect lot number was engraved on the product.

    Product
    Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602 for use as diagnostic contact lenses for eye examinations (including the anterior chamber, trabecular meshwork, central retina, and peripheral retina) and use in the therapy of intraocular abnormalities
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·16V164000·2016-03-22

    Forest River Recalls 2016 Cherokee Grey Wolf Trailers for Placard Error

    Forest River is recalling 2016 Cherokee Grey Wolf recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which may lead to overloading and tire blowouts.

    Product
    CHEROKEE — CHEROKEE GREY WOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0742-2016·2016-03-16

    Urban Oven Cookies Recalled for Undeclared Milk Allergen

    Urban Oven, LLC is recalling specific cookie varieties because the label fails to declare milk, a major food allergen, derived from butter.

    Product
    Urban Oven Artisan-Baked Short Bread Cookies Classic Butter All Natural NET WT. 5 oz. UPC Code: 7 18122 06344 4 SKU #: C1000
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0745-2016·2016-03-16

    Urban Oven Cookies Recalled for Undeclared Milk Allergen

    Urban Oven, LLC is recalling specific cookie varieties because the label fails to declare milk, an ingredient present in the butter used.

    Product
    Urban Oven Artisan-Baked Short Bread Cookies Lemon Pistachio All Natural NET WT. 5 oz UPC Code: 7 18122 06374 1 SKU #: C4000
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0715-2016·2016-03-16

    Cary's Dark Chocolate Almond Toffee Recalled for Soy Allergen Mislabeling

    Cary's of Oregon LLC is recalling Dark Chocolate Almond Toffee with Hawaiian Salt because the packaging fails to declare soy in the 'Contains' statement.

    Product
    Carys Dark Chocolate Almond Toffee with Hawaiian Salt. Product is packaged in printed cardboard packages in 1.3 oz , 4 oz, and 8 oz sizes. There are 12 packages per case. UPC 8 31617 00515, net wt. 1.3 oz. UPC 8 31617 00504, net wt. 4 oz. UPC 8 31617 00580, net wt. 8 oz.
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-0744-2016·2016-03-16

    Urban Oven Cookies Recalled for Undeclared Milk Allergen

    Urban Oven, LLC is recalling four varieties of cookies because the label fails to declare milk, an ingredient present in the butter used.

    Product
    Urban Oven Artisan-Baked Short Bread Cookies Pecan All Natural NET. WT. 5 oz. UPC Code: 7 18122 06364 2 SKU #: C3000
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0723-2016·2016-03-16

    Land O Lakes Margarine Cups Recalled for Missing Allergen Labeling

    Ventura Foods LLC is recalling Land O Lakes margarine cups because they were distributed without labels, failing to disclose milk and soy allergens.

    Product
    Land O Lakes, Fresh Buttery Taste Spread, 48% Vegetable Oil Spread, A product of Land O'Lakes Inc. Arden Hills, MN. Packaged in 5 gram plastic cups.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0743-2016·2016-03-16

    Urban Oven Cookies Recalled for Undeclared Milk Allergen

    Urban Oven, LLC is recalling specific cookie varieties because the label fails to declare milk, an ingredient present in the butter used.

    Product
    Urban Oven Artisan-Baked Short Bread Cookies Cocoa All Natural NET Wt. 5 oz. UPC Code: 7 18122 06354 3 SKU #: C2000
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0739-2016·2016-03-16

    East-West Specialty Sauces Recalls Sweet & Sour Sauce for Allergen Mislabeling

    East-West Specialty Sauces is recalling Classic Sweet & Sour Sauce because Zesty Orange sauce was mislabeled, posing a wheat and soy allergen risk.

    Product
    East-West Classic Sweet & Sour Sauce, 12 fl. Oz., Glass bottle, 6/case, Refrigerate after opening, Distributed by East-West Specialty Sauces, Inc. Denver, CO 80204
    Category
    Food
    Distribution
    2 states