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.

2201–2225 of 9607

  • ModerateFDA (Devices)·Z-1568-2020·2020-04-01

    Signature Orthopaedics Recalls Mislabeled Encina HA Femoral Stem Components

    Signature Orthopaedics is recalling five mislabeled Encina HA Femoral Stem components. The packaging error could cause surgical delays if the wrong product is used.

    Product
    Encina HA Femoral Stem, Size 11 Coxa Vara Collared, REF 100-30-011, Ti6AI4V Allow with HA Coating, For use with Stinson Orthopedics Inc. Total Hip Replacement System Only, CEMENTLESS, UDI: (01) 00841176102934
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-1565-2020·2020-04-01

    Cook Inc. Recalls Pericardiocentesis Sets Due to Incorrect Expiration Dates

    Cook Inc. is recalling 25 Pericardiocentesis Sets because the printed expiration dates are incorrect. The products were distributed to seven US states and Canada.

    Product
    Pericardiocentesis Set, Irrigation Catheter, Reference Part Number C-PCS-700-TORONT0-042997, Order Number G10643
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Drugs)·D-1049-2020·2020-04-01

    FDA Recalls Colostat Homeopathic Remedy Due to Incorrect Labeling

    Grato Holdings, Inc. is recalling 659 bottles of Colostat homeopathic remedy because the indications on the product label are incorrect.

    Product
    COLOSTAT — COLOSTAT (RHAMNUS PURSHIANA, SPIGELIA ANTHELMIA, TARAXACUM OFFICINALE, CAJUPUTUM, HYDRASTIS CANADENSIS, ALUMINA, CINA, CINCHONA OFFICINALIS, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, MANDRAGORA OFFICINARUM, NUX VOMICA)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0845-2020·2020-03-25

    Moonstruck Chocolate Recalls Praline Pecan Bars for Undeclared Milk

    Moonstruck Chocolate Company is recalling Praline Pecan & Ginger Element Bars due to undeclared milk, a major allergen.

    Product
    Moonstruck Praline Pecan & Ginger Element Bar in Dark Chocolate, packaged first into a clear poly film that is sealed. The sealed bar is then packed into a cardboard box (1 bar per box) that has label information. Net wt. 3.1 oz. The product SKU number is 312806 and the UPC code
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0844-2020·2020-03-25

    Pero Family Farms Zucchini Spiral Pesto Recalled for Undeclared Allergens

    Pero Family Farms is recalling Zucchini Spiral Pesto kits due to undeclared egg and milk allergens caused by incorrect labeling.

    Product
    Pero Family Farms Fresh n' Savory Simple Side Kit Zucchini Spiral Pesto; 11 oz. EXP 2020-03-20. Cooks in 5 Minutes
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0840-2020·2020-03-25

    Dole Recalls HEB Tuscan Herb Salad Kits Due to Undeclared Allergens

    Dole Fresh Vegetables Inc is recalling HEB Tuscan Herb Chopped Salad Kits because the included dressing contains peanuts, tree nuts, and wheat not listed on the label.

    Product
    HEB Tuscan Herb Chopped Salad Kit, 12.6 oz. UPC: 0-41220-40989-1
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1507-2020·2020-03-25

    Smith & Nephew Recalls Legion PS Knee Inserts Due to Packaging Error

    Smith & Nephew is recalling 29 Legion PS High Flex XLPE Articular Inserts because they were packaged with an incorrect part.

    Product
    LEGION PS High Flex XLPE size 5-6 9mm Articular Insert
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-1526-2020·2020-03-25

    XTANT Medical Recalls OsteoSelect DBM Putty Due to Volume Discrepancy

    XTANT Medical is recalling 26 units of OsteoSelect DBM Putty because three devices contained 5.0cc instead of the labeled 10.0cc.

    Product
    OsteoSelect Demineralized Bone Matrix (DBM) Putty 10.0cc in a syringe; STERILE R, Product Code: 359100, Dimensions: ONE(1) PACKAGE - CONTAINING 10.0cc. UDI: 00849777003681 - Product Usage: OsteoSelect DBM Putty is indicated for use as a bone void filler and bone graft substitute
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1484-2020·2020-03-25

    Materialise Recalls TRUMATCH Orthognathic Surgical Kit Due to Labeling Error

    Materialise N.V. is recalling TRUMATCH Orthognathic surgical kits because the package labeling indicates a different plate than the one actually included.

    Product
    TRUMATCH Orthognathic - Full Bimaxillary Surgical Kit, Catalog Number SD980.001
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1485-2020·2020-03-25

    Materialise Recalls TRUMATCH Orthognathics Genioplasty Surgical Kit Due to Labeling Error

    Materialise N.V. is recalling TRUMATCH Orthognathics Genioplasty Surgical Kits because the package labeling indicates a different plate than the one actually contained in the kit.

    Product
    TRUMATCH Orthognathics - Genioplasty Surgical Kit, Add-on, Catalog Number: SD980.013
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·20E013000·2020-03-19

    BMW Recalls Motorcycle Brake Fluid Reservoir Caps for Labeling Defect

    BMW is recalling specific motorcycle brake fluid reservoir caps because they may not clearly state the required brake fluid type, potentially leading to improper maintenance.

    Product
    BMW — BMW R NINE T SCRAMBLER, R 1250 R, R 1250 RS, R NINE T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V166000·2020-03-19

    BMW Recalls Motorcycles Due to Unclear Brake Fluid Reservoir Cap Labeling

    BMW is recalling specific 2018-2020 motorcycles because the brake fluid reservoir cap may not clearly state the required fluid type, potentially leading to improper maintenance.

    Product
    BMW — BMW R NINE T SCRAMBLER, R NINE T RACER, R NINE T, R 1250 RS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V155000·2020-03-18

    Daimler Vans Recalls 2018-2019 Sprinter Vehicles for Incorrect Spare Tire Label

    Daimler Vans is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vehicles because the spare tire label may list the maximum speed in kilometers per hour instead of miles per hour.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 1500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0828-2020·2020-03-18

    Barts Ice Cream Recalled for Gluten-Free Mislabeling

    Snow's Acquisition, LLC is recalling Barts Ice Cream Co. Chocolate Chip Cookie Dough ice cream because it is mislabeled as gluten-free despite containing wheat flour.

    Product
    Barts Ice Cream Co. brand of Chocolate Chip Cookie Dough ice cream (Vanilla ice cream with chunks of cookie dough and dark chocolate chips) packaged in a white pint paper container (1 pint) with expiration dates from 03/05/21 through 06/04/21 and UPC#: 048896100169.
    Category
    Food
    Distribution
    2 states
  • HighCPSC·20093·2020-03-18

    Belle Chemical Recalls Sodium and Potassium Hydroxide for Packaging Defects

    Belle Chemical is recalling sodium and potassium hydroxide products because they lack required child-resistant packaging and proper hazard labeling.

    Product
    Sodium Hydroxide, Lye/Caustic Soda and Potassium Hydroxide, Caustic Potash Ash
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0825-2020·2020-03-18

    Harris Teeter Banana Pudding Ice Cream Recalled for Undeclared Soy

    Harris Teeter is recalling Premium Selections Banana Pudding Ice Cream because it contains undeclared soy. Consumers should check their freezers for the affected product.

    Product
    PREMIUM SELECTIONS BANANA PUDDING ICE CREAM NATURALLY & ARTIFICIALLY FLAVORED 1.5 QUART (1.42 L) KEEP FROZEN CONTAINS: MILK, WHEAT, COCONUT OIL, PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC MATTHEWS, NC 28105 877-533-2767 UPC 0 72036 43031 1
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1454-2020·2020-03-18

    Cardinal Health Recalls Non-Sterile Monoject Hypodermic Safety Needles

    Cardinal Health is recalling Monoject Hypodermic Safety Needles because they were shipped as non-sterile despite labeling indicating sterility, posing an infection risk.

    Product
    Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1456-2020·2020-03-18

    Cardinal Health Recalls Non-Sterile Monoject Bluntfill Syringes

    Cardinal Health 200, LLC is recalling Monoject Bluntfill syringes that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.

    Product
    Monoject Bluntfill with Filter, 18G x 1-1/2" Item Code 11811022F. Used for drawing fluid from a vial - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0835-2020·2020-03-18

    Stonewall Kitchen Ghost Pepper Salsa Recalled for Undeclared Allergens

    Stonewall Kitchen is recalling Ghost Pepper Salsa because it contains undeclared milk and soy allergens. Consumers should check their pantry for the specific product.

    Product
    Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato Puree, Green Chile Peppers, Distilled Vinegar, Salt, Dehydrated Ghost Pepper, Dehydrated Garlic, Spices, Dehydrated Cilantro. UPC 7 11381 32738 8. BEST BY 23MAY20
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-1455-2020·2020-03-18

    Cardinal Health Recalls Non-Sterile Hypodermic Safety Needles

    Cardinal Health is recalling Monoject Hypodermic Safety Needles that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.

    Product
    Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1471-2020·2020-03-18

    Verathon Recalls GlideScope Video Laryngoscope Operations and Maintenance Manuals

    Verathon, Inc. is recalling 239 GlideScope Video Laryngoscope Operations & Maintenance Manuals due to a typographical error regarding disinfection instructions.

    Product
    GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
    Category
    Medical Device
    Distribution
    33 states
  • ModerateFDA (Food)·F-0826-2020·2020-03-18

    Siete Grain Free Tortillas Recalled for Sodium Labeling Error

    Garza Food Ventures is recalling Siete Grain Free Burrito Size Tortillas because the sodium content is 340 mg per serving, not the 15 mg declared on the label.

    Product
    Siete Grain Free Burrito Size Tortillas Net Wt 15 oz (423g) 6 count UPC 865336000083 packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateCPSC·20094·2020-03-18

    Belle Chemical Recalls Drain Cleaner for Missing Poison Labeling

    Belle Chemical is recalling 100% Sodium Hydroxide Drain Cleaner because the label violates the Federal Hazardous Substance Act by omitting the word 'poison' and mandatory hazard statements.

    Product
    100% Sodium Hydroxide Drain Cleaner
    Category
    Consumer Product
    Distribution
    Distributed nationwide