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.

2051–2075 of 9607

  • ModerateFDA (Devices)·Z-1931-2020·2020-05-20

    Ortho-Clinical Diagnostics Recalls VITROS CKMB Slides Due to Incorrect Instructions

    Ortho-Clinical Diagnostics is recalling VITROS CKMB Slides because Spanish and Swedish instructions incorrectly state the assay can be tested with plasma, which could result in biased results.

    Product
    VITROS Chemistry Products CKMB Slides, Creatine Kinase MB, Product Code 8001133-90 slides, UDI Number 10758750004201 - Product Usage: The VITROS Chemistry Product Slides are used to measure creatine kinase MB (CK-MB) activity in serum which used to be ordered to detect Myocardial
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2005-2020·2020-05-20

    Genicon EZee Specimen Retrieval Bag Recall for Labeling Clarity

    Genicon is recalling 1,550 units of the EZee Single Use Specimen Retrieval Bag to provide updated labeling instructions for multiple specimen retrieval.

    Product
    Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: This device is disposable and is packaged and sterilized for single use only. The bag may be used for multiple specimen retraction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1946-2020·2020-05-20

    Becton Dickinson Recalls PowerGlide ST Midline Catheter Kits Missing Lidocaine

    Becton Dickinson is recalling 655 PowerGlide ST Midline Catheter Maximal Barrier Kits because they were packaged without the required lidocaine.

    Product
    PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1941-2020·2020-05-20

    Medtronic Recalls Vertex Select Multi Axial Screws Due to Length Discrepancy

    Medtronic is recalling 83 Vertex Select Multi Axial Screws because the product length is shorter than labeled. The recall covers units distributed in California and Michigan.

    Product
    VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0936-2020·2020-05-13

    La Sonorense Recalls Whole Wheat Flour Tortillas for Undeclared Wheat

    La Sonorense, Inc. is recalling whole wheat flour tortillas because the packaging does not properly display the ingredient list and contains undeclared wheat.

    Product
    14", 10" Hand Stretched Whole Wheat Flour Tortillas, packaged in quantities of 1-2 dozen per package. Each package is twist-tied and placed in a box. Box is then sealed for delivery.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0932-2020·2020-05-13

    Aldi Recalls Organic Red Split Lentils for Undeclared Wheat

    Aldi is recalling Simply Nature Organic Red Split Lentils because the product may contain undeclared wheat. This poses a risk to individuals with wheat allergies or celiac disease.

    Product
    Simply Nature Organic Red Split Lentils, 16 oz bag, UPC 041498299507
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0934-2020·2020-05-13

    La Sonorense Pressed Wheat Flour Tortillas Recalled for Undeclared Wheat

    La Sonorense, Inc. is recalling pressed wheat flour tortillas because the product does not properly display the list of ingredients and contains undeclared wheat.

    Product
    12", 10" Pressed Wheat Flour Tortillas, packaged in quantities of 1-2 dozen per package. Each package is twist-tied and placed in a box. Box is then sealed for delivery.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0935-2020·2020-05-13

    La Sonorense Wheat Flour Tortillas Recalled for Undeclared Wheat

    La Sonorense, Inc. is recalling hand-stretched wheat flour tortillas because the product does not properly display the list of ingredients and contains undeclared wheat.

    Product
    16", 14", 13", 12", 10", 5" Hand Stretched Wheat Flour Tortillas, packaged in quantities of 1-2 dozen per package. Each package is twist-tied and placed in a box. Box is then sealed for delivery.
    Category
    Food
    Distribution
    1 state
  • HighUSDA FSIS·010-2020·2020-05-13

    Evans Food Group Recalls Pork Skin Products Due to Undeclared Soy

    Evans Food Group is recalling ready-to-eat pork skin products because the variety pack label fails to declare soy, a known allergen.

    Product
    Evans Food Group — Evans Food Group Recalls Ready-To-Eat Pork Skin Products due to Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1850-2020·2020-05-13

    Epimed RF Injector Cannula Recalled for Incorrect Expiration Date Labeling

    Epimed International is recalling 701 units of R-F Injector Cannulas due to incorrect expiration dates on the packaging. The devices were distributed worldwide and across multiple US states.

    Product
    R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124; REF/UDI: 257-2010D(01)00818788022127 - Product Usage:The Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1851-2020·2020-05-13

    Nobel Biocare Dental Implant Recall Due to Incorrect Length Labeling

    Nobel Biocare is recalling 228 dental implants because the packaging label incorrectly lists the length as 7mm instead of the actual 10mm.

    Product
    NobelParallel Conical Connection NP, 3.75x10mm (Endosseous Dental Implant); REF 37965; UDI (01)07332747091441(10)12129104(17)240203 - Product Usage: are intended to be used in the upper or lower jaw bone (osseointegration) and used for anchoring or supporting tooth replacements
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1892-2020·2020-05-13

    Trilliant Surgical Recalls 3.5mm Aresenal Screw Drill Bits Due to Labeling Error

    Trilliant Surgical, LLC is recalling 3.5mm Aresenal Screw Drill Bits due to a labeling error where the lot number is incorrectly marked, potentially impacting device traceability.

    Product
    3.5mm Aresenal Screw Drill Bit , Ref: 330-35-001, Qty. 70, Rx Only, Non-Sterile, UDI: (01)00812926029696 - Product Usage: A drill bit facilitates implant insertion
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1849-2020·2020-05-13

    Epimed RF Injector Cannula Recalled for Incorrect Expiration Date

    Epimed International is recalling 1,374 units of RF Injector Cannulas due to incorrect expiration dates on the packaging.

    Product
    R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 - Product Usage: The Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0925-2020·2020-05-06

    Whole Foods Market Recalls Minestrone Soup for Undeclared Milk

    Whole Foods Market is recalling Minestrone Soup sold in deli containers and bags because it may contain undeclared milk.

    Product
    Whole Foods Market Minestrone Soup PLU code printed on the product scale labels beginning with 248529 for soup sold in clear plastic deli-style containers of various weight and 246691 for soup sold in clear plastic bags weighing 7 lbs. 12 oz.
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-1802-2020·2020-05-06

    Stryker Recalls 90 Reprocessed Zimmer Tourniquet Cuffs Due to Mislabeling

    Stryker Sustainability Solutions is recalling 90 reprocessed Zimmer tourniquet cuffs because they are potentially mislabeled. The mislabeling could lead to device misuse or inadequate limb compression during surgery.

    Product
    Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number: 60-7070-105, UDI: 00885825013868, Reprocessed Tourniquet Cuff - Product Usage: Reprocessed tourniquet cuffs are indicated for use in patients who require surgery of the extremities with an expected dur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1820-2020·2020-05-06

    Smiths Medical Recalls Mislabeled Portex Lumbar Puncture Trays

    Smiths Medical ASD Inc. is recalling 100 units of Portex Lumbar Puncture Trays because the inner trays were mislabeled with an incorrect model number.

    Product
    Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product Usage: Portex lumbar puncture trays provide all the materials necessary to measure cerebrospinal fluid pressure and/or collect cerebrospinal fluid specimens. Key components include skin prep materials, la
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0921-2020·2020-05-06

    XinXing Dried Plum Recalled for Mislabeling Dried Peaches

    Rong Shing Trading NY Inc is recalling XinXing Dried Plum because the product contains dried peaches, which are not listed on the front label.

    Product
    XinXing Dried Plum, Net Wt. 5.3 oz.(150g)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1833-2020·2020-05-06

    Baxter Prismaflex System Recall for Connector Usage Safety Information

    Baxter Healthcare is issuing a Class II recall for 133 Prismaflex Systems to communicate safety information regarding the proper use of connectors.

    Product
    Prismaflex System, Prismaflex Control Unit
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Food)·F-0930-2020·2020-05-06

    Golden Nutrition Recalls Biotin Supplement Due to Low Content

    Golden Nutrition is recalling Biotin 1000mcg tablets because FDA testing found the biotin content was only 0.8% of the label claim.

    Product
    Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition
    Category
    Food
    Distribution
    0 states
  • LowFDA (Food)·F-0926-2020·2020-05-06

    Calci-Max Dietary Supplement Recalled for Zinc Content Deficiency

    Alfa Vitamins Laboratories is recalling Calci-Max dietary supplements because FDA testing found the product contained 0.0% of the labeled zinc content.

    Product
    CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
    Category
    Food
    Distribution
    0 states
  • HighUSDA FSIS·PHA-05022020·2020-05-02

    Chicken Noodle Soup Recalled for Undeclared Egg Allergen

    USDA issued a public health alert for Roundy's chicken noodle soup containing undeclared egg. No illnesses have been reported.

    Product
    Roundy's Supermarkets, Inc. — FSIS Issues Public Health Alert for Chicken Noodle Soup Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V247000·2020-05-01

    Mercedes-Benz Recalls G-Class Vehicles Due to Child Safety Lock Label Error

    Mercedes-Benz is recalling 2019-2020 G550 and G63 vehicles because the child safety lock symbol may indicate the incorrect status, posing a risk to unrestrained children.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 550, G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0933-2020·2020-04-29

    Champlain Chocolate Company Recalls Dark Chocolate Coins for Undeclared Milk

    Champlain Chocolate Company is recalling specific lots of Lake Champlain Dark Chocolate Coins because they contain undeclared milk, a major allergen.

    Product
    Lake Champlain CHOCOLATES, COIN DARK BULK ORG, NET WT 48 OZ (1.3 kg), APPROX 186 PIECES, INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, COCOA POWDER (PRESSED WITH ALKALI), AND VANILLA POWDER) MAY CONTAIN TRACES OF MILK, PEANUTS, SOYBEAN, TREE NUTS, AND WHEAT
    Category
    Food
    Distribution
    6 states