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.

6026–6050 of 9610

  • SevereFDA (Food)·F-0265-2016·2015-12-02

    TN Juice Bar Recalls Refine 3-Day Cleanse Juice Kit Nationwide

    TN Juice Bar is recalling 137 units of the Refine 3-Day Cleanse juice kit nationwide due to unpasteurized juice with elevated pH levels and unlabeled almond milk.

    Product
    Refine 3-Day Cleanse, a juice kit that contains Lean Green, 16 oz (6 bottles), Beet It, 16 oz (6 bottles), Almond Milk, 8 oz (3 bottles) and Wheat grass juice, 8 oz (2 bottles)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0287-2016·2015-12-02

    Meijer Caramel Corn Recalled for Undeclared Milk Allergen

    Meijer Distribution is recalling Caramel Corn because the label lists butter but fails to declare the presence of milk, a major allergen.

    Product
    Meijer Caramel Corn, packed in 10 oz. bags, ( 283 g), 12 bags per case
    Category
    Food
    Distribution
    4 states
  • LowFDA (Devices)·Z-0322-2016·2015-12-02

    Lab Vision p21 WF1 Antibody Recalled for Incorrect Concentration Labeling

    Lab Vision Corporation is recalling p21 WF1 Ab-3 antibody vials because the label incorrectly states the concentration as 0.2 mg/ml instead of the actual 0.4 mg/ml.

    Product
    Thermo Scientific p21 WF1 Ab-3 (DCS-60.2) 1 ml (0.4mg/ml): Product code: MS-230-P and MS-230P0; Hematology: p21WAF1/Cip1/Sdi1/Pic1 is a tumor suppressor protein. Expression of p21WAF1 is induced by wild type, but not mutant, p53 suppressor protein. The p21WAF1 protein binds
    Category
    Medical Device
    Distribution
    2 states
  • LowFDA (Devices)·Z-0328-2016·2015-12-02

    Biochemical Diagnostics Recalls hCG Control Kits Due to Labeling Discrepancies

    Biochemical Diagnostics Inc. is recalling CONSULT hCG Controls Kits because storage temperature instructions on the kit labels do not match the vial labels and package insert.

    Product
    CONSULT(TM) diagnostics hCG CONTROLS Kit, Part/Reorder Number 5011, IVD Product Usage - CONSULT Diagnostics hCG Controls are intended to validate the performance of qualitative hCG urine procedures and immunochromatographic devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0323-2016·2015-12-02

    Synthes 2.4mm Locking Screws Recalled for Incorrect Package Insert

    Synthes (USA) Products LLC is recalling 229 units of 2.4mm Locking Screws because they may contain the wrong package insert.

    Product
    2.4MM locking screw SLF-TPNG with Stardrive Recess 18 mm. Intended for fixation of fractures, osteotomies, nonunions, replantations, and fusions of small bones and small bone fragments, particularly in osteopenic bone.
    Category
    Medical Device
    Distribution
    27 states
  • HighUSDA FSIS·143-2015·2015-11-25

    Boyle's Famous Corned Beef Recalls Beef Top Round for Undeclared Wheat

    Boyle's Famous Corned Beef Co. is recalling seasoned beef top round cases because the product contains undeclared hydrolyzed wheat protein, a known allergen.

    Product
    Boyle's Famous Corned Beef (2024), LLC — Boyle's Famous Corned Beef Co. Recalls Beef Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0228-2016·2015-11-25

    Kanan Enterprises Recalls Mountain Mix for Undeclared Milk

    Kanan Enterprises is recalling Mountain Mix trail mix products because they contain undeclared milk. The products were distributed to 21 states and Canada.

    Product
    Mountain Mix 2oz bag, 7oz pouch, 10oz pouch, 17oz tin, 28oz pouch & 25lb bag. INGREDIENTS: Raisins, Peanuts (Peanuts, Peanut and/or Canola Oil, Salt), Choco Buttons (Sugar, Partially Hydrogenated Vegetable Oil [Contains One or More of the Following: Palm Kernel***Produced in a fa
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-0262-2016·2015-11-25

    Ocean's Halo Seaweed Chips Recalled for Gluten Contamination

    New Frontier Foods is recalling Ocean's Halo Seaweed Chips because routine tests found gluten levels above the FDA limit for gluten-free products.

    Product
    Ocean's Halo, The Seaweed Chip. Sea Salt Flavor; 2.5 oz. bag Organic and Gluten Free ingredients. USDA Organic. Outer Case UPC: 10851899005174 Unit (Bag) UPC: 8 51899 00517 7 Distributed by New Frontier Foods, Inc. Burlingame, CA.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0219-2016·2015-11-25

    NatureBox Sticks 'n Stones recalled for potential peanut contamination

    NatureBox is recalling Sticks 'n Stones trail mix because the oil used to roast nuts was also used for peanuts, which are not listed on the label.

    Product
    NatureBox Sticks 'n Stones; roasted nuts with sesame sticks 4.5 oz (128 g) pouches - UPC 8 52523 00546 4 and 5 lb. Corporate bags - no UPC; Ingredients: Sesame Sticks (unbleached flour, malted barley flour, soybean oil, sesame seeds, bulgar wheat, salt, beet powder, turmeric)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0272-2016·2015-11-25

    Precision Medical Recalls Easy Dial Oxygen Regulators Due to Label Error

    Precision Medical is recalling 315 Easy Dial Oxygen Regulators because the settings label may be off by one position, causing incorrect oxygen flow.

    Product
    Easy Dial Oxygen Regulator, 168708D and 168715D. Eight liter from .0.25 to 8 liters, 15 liter from 0.5 liter to 15 liters of oxygen per minute.
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Food)·F-0263-2016·2015-11-25

    Ocean's Halo Seaweed Chips Recalled for Gluten Contamination

    New Frontier Foods is recalling Ocean's Halo Chili Lime Seaweed Chips because routine tests found gluten levels above the FDA limit for gluten-free products.

    Product
    Ocean's Halo, The Seaweed Chip. Chili Lime Flavor; 2.5 oz. bag Organic and Gluten Free ingredients. USDA Organic. Outer Case UPC: 10851899005198 Unit (Bag) UPC: 8 51899 00519 1 Distributed by New Frontier Foods, Inc. Burlingame, CA.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0279-2016·2015-11-25

    Astora Recalls MiniArc Pro Sling System Due to Labeling Mismatch

    Astora is recalling 52 units of the MiniArc Pro Single incision Sling System because the lot number on the outer carton did not match the labels inside the box.

    Product
    MiniArc Pro Single incision Sling System, Model number / Product Reference 9000261, Lot 936405xxx. Designed to treat female stress urinary incontinence.
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0318-2016·2015-11-25

    TZ Medical Recalls SilverStat Hemostasis Pads Due to Labeling Discrepancy

    TZ Medical Inc. is recalling 10,180 units of SilverStat hemostasis pads because the instructions for use did not match the original FDA submission.

    Product
    SilverStat, sterile 2" x 2 " calcium alginate hemostasis pad with sliver nitrate, Part number 8870-07. Product Usage: SilverStat is an effective barrier to microbial penetration for moderate to heavy exudating partial and full-thickness wounds, including pressure ulcer
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Food)·F-0187-2016·2015-11-25

    Herr's Potato Chips Recalled for Incorrect Gluten-Free Labeling

    Herr's Foods is recalling Sour Cream & Onion Potato Chips because packaging incorrectly states the product is gluten-free, despite containing wheat.

    Product
    Herr's Sour Cream & Onion Flavored Potato Chips
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Food)·F-0188-2016·2015-11-25

    Enjoy Life Semi-Sweet Chocolate Mini Chips Recalled for Undeclared Allergens

    Enjoy Life Natural Brands is recalling Semi-Sweet Chocolate mini chips because they may contain undeclared sunflower seeds, pumpkin seeds, and dried fruit.

    Product
    Semi-Sweet Chocolate mini chips packaged in a plastic bad with yellow label and white lettering.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0293-2016·2015-11-25

    TZ Medical Neptune Plus Hemostasis Pad Recall for Labeling Mismatch

    TZ Medical Inc. is recalling Neptune Plus hemostasis pads because the instructions for use do not match the original FDA submission.

    Product
    Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath removal, Part number 8870-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0264-2016·2015-11-25

    Ocean's Halo Seaweed Chips Recalled for Gluten Contamination

    New Frontier Foods is recalling Ocean's Halo Korean BBQ Seaweed Chips because routine tests found gluten levels above the FDA limit for gluten-free products.

    Product
    Ocean's Halo, The Seaweed Chip. Korean BBQ Flavor; 2.5 oz. bag Organic and Gluten Free ingredients. USDA Organic. Outer Case UPC: 10851899005181 Unit (Bag) UPC: 8 51899 00518 4 Distributed by New Frontier Foods, Inc. Burlingame, CA.
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·15V784000·2015-11-23

    Crossroads ReZerve Travel Trailer Recall for Incorrect Axle Labeling

    Crossroads RV is recalling 2016 ReZerve travel trailers because the Federal Identification Label incorrectly states the axle capacity, potentially leading to overloading and loss of control.

    Product
    CROSSROADS — CROSSROADS REZERVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0234-2016·2015-11-18

    Miramar Labs Recalls miraDry System for Labeling Update on Lubricant Use

    Miramar Labs is recalling 277 miraDry Systems to update labeling that reminds users to use only approved lubricants in a thin layer to prevent burns and blisters.

    Product
    miraDry System consisting of the MD4000-MC Console, the MD4000-HP miraDry Handpiece, and the MD4000-BT miraDry bioTip and accessories. General and Plastic Surgery: The miraDry System is intended for the treatment of primary axillary hyperhidrosis and was recently cleared for t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0237-2016·2015-11-18

    Tekia Recalls Intraocular Lenses Due to Incorrect Diopter Power Labeling

    Tekia is recalling 50 units of Single Piece Hydrophilic Acrylic Intraocular Lenses because they may be labeled with the incorrect diopter power.

    Product
    TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0239-2016·2015-11-18

    Beckman Coulter Recalls Access CEA Assay Reagent Packs for Filling Errors

    Beckman Coulter is recalling Access CEA Assay reagent packs because they were filled incorrectly. The recall covers 11,406 units distributed worldwide.

    Product
    Access CEA Assay, Part No. 33200. For the quantitative determination of Carcinoembryonic Antigen (CEA) levels in human serum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0266-2016·2015-11-18

    Biomet 3i Dental Driver Tips Recalled for Mislabeling

    Biomet 3i is recalling 96 dental driver tips because hexed tips were labeled as square tips, and square tips were marked with hexed identifiers.

    Product
    Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver tips are attached to a surgical drilling unit to carry components such as implant mounts, healing abutments and screws for placement and removal. For dental and restorative procedures.
    Category
    Medical Device
    Distribution
    30 states