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.

6151–6175 of 9610

  • ModerateFDA (Food)·F-3258-2015·2015-10-07

    Coquette's Gluten Free Cupcakes Recalled for Incorrect Allergen Labeling

    Coquette's Bistro and Bakery is recalling 120 packages of gluten-free cupcakes because the label incorrectly states the product contains no egg or dairy, despite containing both.

    Product
    Coquette's Gluten Free Spring Pack Cupcakes (4 pack), Oranges n' Cream & Strawberry Mint Lemonade. coquettesbistro.com. NET Wt. 9.67 OZ. No expiration date on package, sold in ambient air at retail.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-3245-2015·2015-09-30

    Majopa Graviola Extract Recalled for Unapproved Drug Claims

    Majopa Industries is recalling 500 bottles of Graviola Extract sold in Puerto Rico because the label made unapproved drug claims, including cancer treatment.

    Product
    Label reads in part as: "GRAVIOLA EXTRACT***1 FL Oz (30 ml)*** ORIGINAL FORMULA***Manufactured by: Majopa Industries Corp.*** PRODUCT OF PUERTO RICO,USA". Drug claims in the product label are as follows: "Researchers have found that Extracts from Graviola leaves can produce ac
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-3242-2015·2015-09-30

    Hillside Quickie Too Recalls Seitan Steak Sandwiches for Allergen Mislabeling

    Hillside Quickie Too is recalling Seitan Steak sandwiches because the wheat bun was not listed in the 'Contains' statement, posing a risk to consumers with wheat allergies.

    Product
    Seitan Steak is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-3243-2015·2015-09-30

    Hillside Quickie Too Tofustrami Recalled for Allergen Mislabeling

    Hillside Quickie Too is recalling Tofustrami sandwiches because the wheat bun ingredient was not listed in the allergen statement.

    Product
    Tofustrami is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-3239-2015·2015-09-30

    Hillside Quickie Too Recalls Tofu Sandwiches Due to Undeclared Wheat

    Hillside Quickie Too is recalling New York Deli Tofu sandwiches in Washington because the product contains wheat but the label does not declare it.

    Product
    New York Deli Tofu is is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-3241-2015·2015-09-30

    Hillside Quickie Too Recalls Jamaican Spice Tempeh Sandwiches for Allergen Mislabeling

    Hillside Quickie Too is recalling Jamaican Spice Tempeh sandwiches because the wheat bun was not listed in the 'Contains' allergen statement, posing a risk to consumers with wheat allergies.

    Product
    Jamaican Spice Tempeh is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2805-2015·2015-09-30

    Fujifilm EPX 2500 Operation Manual Recalled for Incorrect Endoscope Specifications

    Fujifilm is recalling 60 EPX 2500 Operation Manuals and sales brochures that incorrectly identify the ED-530XT endoscope's image capabilities.

    Product
    Fujinon/Fujifilm Processor EPX 2500 Operation Manual. For use in endoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2811-2015·2015-09-30

    Synthes Cranial Flap Tube Clamp Recalled for Incorrect MR Safe Labeling

    Synthes (USA) Products LLC is recalling Cranial Flap Tube Clamps and Crimping Devices because they were labeled MR Safe without required testing protocols.

    Product
    Synthes Cranial Flap Tube Clamp and Crimping Device Product Usage: The Synthes Cranial Flap Tube Clamp System is intended to reattach a cranial bone flap to the surrounding cranium after a craniotomy procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2796-2015·2015-09-30

    OrthoPediatrics Recalls 3.5mm Non Locking Cortical Screws Due to Packaging Error

    OrthoPediatrics Corp is recalling 3.5mm Non Locking Cortical Screws because the packaging may contain a different screw size than labeled.

    Product
    3.5mm Non Locking Cortical Screw, in the PediLoc Tibial Plate System Part number 00-0903-2510, 3.5mm x 10mm Non Locking Cortical Screw. Used in pediatric orthopedics.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2808-2015·2015-09-30

    Bard Access Systems Recalls PowerPICC Catheter Marketing Brochures

    Bard Access Systems is recalling 1,811 marketing brochures for PowerPICC and PowerPICC SOLO catheters because they contain incorrect indications for use.

    Product
    Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-2806-2015·2015-09-30

    Fujifilm EPX 2500 Processor Manual and Brochure Recall

    Fujifilm is recalling EPX 2500 Processor manuals and brochures that incorrectly identify the ED-530XT endoscope's image quality.

    Product
    Fujifilm Processor EPX 2500 High Definition Endoscopy; (Sales Brochure). For use in endoscopic procedures. Used to observe, record and capture images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2817-2015·2015-09-30

    BD Biosciences Recalls CD4 FITC Reagent Due to Spanish Labeling Error

    Becton, Dickinson and Company is recalling 128 units of CD4 (SK3), FITC reagent because the Spanish text on the label incorrectly identifies the product as CD8 FITC.

    Product
    CD4 (SK3), FITC; Contains CD4 FITC with gelatin and 0.1% sodium Azide. Catalog number 340133 in vitro diagnostic used in Hematology: The SK3 monoclonal antibody reacts with human CD4, a 59-kDa cell surface receptor expressed by a majority of thymocytes, a subpopulation of ma
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·125-2015·2015-09-25

    Calperf Recalls Marinated Chicken Product Due to Undeclared Milk Allergen

    Calperf is recalling approximately 216 pounds of marinated chicken product because it contains milk, a known allergen, that is not declared on the ingredient list.

    Product
    CREATIVE FOOD PROCESSING — Calperf Recalls Chicken Product Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-3226-2015·2015-09-23

    KellBran Caramel Popcorn Recalled for Undeclared Milk Allergen

    KellBran Candies is recalling 8 oz. bags of creamy rich caramel popcorn because the product may contain undeclared milk, a major food allergen.

    Product
    KellBran" CANDIES, INC. creamy rich caramel popcorn Net Wt. 8 oz. (226.64 Grams) ALLERGY INFO: Manufactured in a facility that processes peanuts, nuts, soy and milk. UPC 0 96637 50153 9 kellbrancandies.com KellBran Candies, Inc. Akron, Ohio 44312
    Category
    Food
    Distribution
    27 states
  • HighFDA (Food)·F-3231-2015·2015-09-23

    Valley View Orchard Pies Recalls Blueberry Crisp for Undeclared Soy

    Valley View Orchard Pies Inc. is recalling Blueberry Crisp products due to undeclared soy lecithin. The products were distributed in Maine, New Hampshire, and Massachusetts.

    Product
    Valley View Orchard Pies, Blueberry Crisp
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2760-2015·2015-09-23

    Biomet 3i Recalls Mislabelled UCLA Dental Abutment Cylinders

    Biomet 3i is recalling 61 UCLA Abutment Hexed Castable Cylinders because they were mislabeled as a different model. The error affects one specific lot distributed worldwide.

    Product
    UCLA Abutment Hexed Castable Cylinder 3.4mm Are accessories to endosseous dental implant to support a prosthetic device in a partially or completely edentulous patient.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-2773-2015·2015-09-23

    Pointe Scientific Creatinine Reagent Recall Due to Labeling Error

    Pointe Scientific is recalling 93 kits of Creatinine Reagent C7539-150 because the R1 and R2 reagent bottles are mislabeled, which prevents valid test results.

    Product
    Pointe Scientific Creatinine Reagent Catalog number C7539-150 in vitro diagnostic C7539-150 kit includes one R1 and one R2 bottle. R1: HDPE plastic bottle. 120 ml fill. R2: HDPE plastic bottle. 90 ml fill.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·15T020000·2015-09-22

    Michelin Recalls X Works Tires for Missing Required Markings

    Michelin is recalling specific X Works XZY tires because they lack required DOT symbols and load range letters, which may cause confusion with non-compliant tires.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·15V579000·2015-09-21

    Mitsubishi Recalls 2011 Outlander Sport for Incorrect Certification Labels

    Mitsubishi is recalling 2011 Outlander Sport vehicles manufactured on December 3, 2010, due to incorrect certification labels lacking the correct VIN. Dealers will install corrected labels free of charge.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2741-2015·2015-09-16

    Siemens Recalls Dimension CREA Tests for Falsely Depressed Results

    Siemens Healthcare Diagnostics is recalling Dimension CREA and Dimension Vista CREA tests because they may produce falsely depressed creatinine results in the presence of hemolysis.

    Product
    Dimension¿ CREA (Creatinine) and Dimension Vista¿ CREA (Creatinine); The CREA method used on the Dimension¿ clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of creatinine in human serum, plasma and urine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2744-2015·2015-09-16

    Biomet C-Tek Maxan Anterior Cervical Plate System Mislabeled Recall

    Biomet Spine is recalling 7 parts of the C-Tek Maxan Anterior Cervical Plate System because some units were mislabeled with an incorrect part number.

    Product
    Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1419-2015·2015-09-16

    CVS Sugar Free Black Cherry Cough Drops Recalled for Foreign Tablets

    Bestco, Inc. is recalling CVS Sugar Free Black Cherry Cough Drops because they may contain comingled Sugar Free Honey Lemon cough drops.

    Product
    CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT), Packaged in a) 25 Drop Bags (UPC: 050428 448526) and b) 36 drop bags (UPC: 050428 476581), Over the Counter. Distributed by: CVS Pharmacy, Inc., One CVS Drive Woonsocket, RI 02895.
    Category
    Drug
    Distribution
    Distributed nationwide