The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 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 589 (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.

6876–6900 of 9611

  • ModerateFDA (Devices)·Z-0502-2015·2014-12-10

    Aesculap Dual Switch Valve Recalled for Incorrect Expiration Date Labeling

    Aesculap, Inc. is recalling three Dual Switch Valves due to incorrect expiration dates on inner sterile bag labels. No patient injuries have been reported.

    Product
    The Dual Switch Valve is used for fluid drainage from the ventricles into the peritoneum, in cases of hydrocephalus.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0479-2015·2014-12-10

    Stryker GDC 360 Coils Recalled for Expiration Date Violations

    Stryker Neurovascular is recalling GDC 360 coils, Target coils, and Gateway PTA Balloon Catheters shipped to US customers beyond their expiration dates.

    Product
    GDC-10 360 10mm x 30cm SR ; GDC 360¿ Detachable Coils are intended for embolization of those intracranial aneurysms that- because of their morphology, their location, or the patient 's general medical condition - are considered by the treating neurosurgical team to be a)
    Category
    Medical Device
    Distribution
    4 states
  • LowFDA (Drugs)·D-0289-2015·2014-12-10

    Zydus Recalls Benzonatate Capsules Due to Foreign Capsule Contamination

    Zydus Pharmaceuticals USA is recalling Benzonatate 200 mg capsules because they may contain foreign 100 mg capsules.

    Product
    BENZONATATE Capsules, USP, 200 mg, 100 Capsule Bottles, Rx only. Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA, Inc. NDC: 68382-248-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0488-2015·2014-12-10

    CooperSurgical Cannula-Curette Recalled for Incorrect Curette Type

    CooperSurgical is recalling 30 units of the Cannula-Curette 12MM (Lot 147234) because the product contains an incorrect curette type.

    Product
    Cooper Surgical CANNULA-CURETTE 12MM; Model Number: MX562 The CooperSurgical SUCTION CANNULA-CURETTE device is used to remove tissue from within the uterine cavity on an outpatient basis. The primary uses for this device are for endometrial sampling especially of those patient
    Category
    Medical Device
    Distribution
    3 states
  • HighNHTSA·14V782000·2014-12-09

    Starcraft RV Recalls 2015 Launch Ultra Lite Travel Trailers for Tire Label Error

    Starcraft RV is recalling 2015 Launch Ultra Lite travel trailers because tire labels list incorrect pressure information, which could lead to over-inflation and tire blowouts.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT redundant LAUNCH, LAUNCH ULTRA LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V775000·2014-12-05

    Jayco Eagle Fifth Wheel Trailers Recalled for Incorrect Tire Size Labels

    Jayco is recalling 2015 Eagle HT FW 28.5RSTS "PR" trailers because incorrect tire size information on the label could lead to improper tire replacement and increased crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0573-2015·2014-12-03

    Karlsburger Foods Recalls Low Sodium Taco Seasoning for Undeclared Milk

    Karlsburger Foods is recalling Low Sodium Taco Seasoning because it contains milk, an allergen not declared on the label.

    Product
    Karlsburger Foods Low Sodium Taco Seasoning, Item Numbers 16423 (Packaged in 23 oz resealable plastic containers), Item #16465 (Packaged in 6.8 lb. resealable plastic containers), and Item #16425 (Packaged in 25 lb. bag in a box).
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-0484-2015·2014-12-03

    CooperSurgical LEEP Loop Electrode Recalled for Outer Box Mislabeling

    CooperSurgical is recalling LEEP Radius Loop Electrodes because the outer box is mislabeled with the wrong part number.

    Product
    CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D, 12 cm shaft ). Box of 5 Model Number(s): R2010 Intended Use: Diagnosis and treatment of non-invasive HPV-related or unrelated lesions of the lower genital tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0256-2015·2014-12-03

    Baxter Recalls Potassium Chloride Injection Bags Due to Labeling Error

    Baxter Healthcare is recalling 63,360 bags of Potassium Chloride Injection due to incorrect outer packaging labels indicating a higher strength.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0449-2015·2014-12-03

    Remel TB Potassium Permanganate Stain Recalled for Performance Issues

    Remel Inc is recalling TB Potassium Permanganate stain due to potential cloudiness or discoloration that may affect mycobacterial diagnosis.

    Product
    Remel TB Potassium Permanganate (.5% Aqueous) 40192, packaged in 250 ml bottles, 5/pkg. A stain for use in qualitative procedures as a counterstain in the fluorescent microscopic detection of mycobacteria.
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-0418-2015·2014-12-03

    Materialise Recalls Zimmer Patient Specific Instrument PERSONA CR Pin Guides

    Materialise USA LLC is recalling specific Zimmer Patient Specific Instrument PERSONA CR Pin Guides because the packaging contained incorrect components and one guide exceeded size specifications.

    Product
    Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Tibia) is intended to be used as a surgical instrument to assist in the positioning of Total Knee Replacement components intraoperatively and in guiding the marking of bone before cutting provided that anatomic l
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0467-2015·2014-12-03

    Biomerica Recalls Calcitonin ELISA Kits Due to Potential False High Values

    Biomerica is recalling Calcitonin ELISA Kits because they may produce false high values. The recall covers 1,062 units distributed worldwide.

    Product
    Calcitonin ELISA Kit, Code No. 7024, 7024BU. Intended use of this product is the quantitative determination of Calcitonin in human serum.
    Category
    Medical Device
    Distribution
    4 states
  • LowFDA (Devices)·Z-0470-2015·2014-12-03

    Novadaq Non-Sterile Drape Recalled for Incorrect Sterile Labeling

    Novadaq Technologies is recalling 324 non-sterile LUNA drapes that were inadvertently mislabeled with an additional contents sterile label.

    Product
    Non-sterile drape
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0469-2015·2014-12-03

    Novadaq LUNA Chest Recalled for Sterile Labeling Error

    Novadaq Technologies is recalling 828 LUNA Chest units because non-sterile drapes were inadvertently mislabeled as sterile.

    Product
    LUNA Chest, Model No. LU4006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0519-2015·2014-11-26

    Welcome Market Coconut Toast Recalled for Missing Allergen Statements

    Welcome Market Inc is recalling Coconut Toast products due to missing allergen statements for wheat, soy, and/or milk. The recall affects 3,133 loaves sold in Northern California and Washington.

    Product
    Coconut Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0518-2015·2014-11-26

    Welcome Market Recalls Green Onion Pork Sung Toast for Allergen Mislabeling

    Welcome Market Inc is recalling Green Onion Pork Sung Toast sold at 99 Ranch Market in Northern California and Washington due to missing allergen statements for wheat, soy, and milk.

    Product
    Green Onion Porksung Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0533-2015·2014-11-26

    InHarvest Garden Vegetable Seasoning Recalled for Undeclared Milk

    InHarvest is recalling Garden Vegetable Seasoning because it contains milk, which is not declared on the label.

    Product
    Whole Grain 5 Blend/Garden Vegetable 12/36 oz Product number 12410; Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed Corn Protein, Sun-Dried Tomato, Salt, Autolyzed Yeast Extract
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0516-2015·2014-11-26

    Welcome Market U-TA-NE Toast Recalled for Missing Allergen Information

    Welcome Market Inc is recalling U-TA-NE Toast products because they lack required allergen statements for wheat, soy, and/or milk.

    Product
    U-TA-NE Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0504-2015·2014-11-26

    Original Soup Man Recalls Lobster Bisque for Undeclared Seafood Allergens

    Original Soup Man is recalling Lobster Bisque due to undeclared shrimp, tilapia, and perch. Consumers should check lot numbers and stop consuming the product.

    Product
    THE ORIGINAL SOUPMAN Lobster Bisque, Net Wt 17 oz (482 g). Product is packed as a tetra pak and ships as a pack of 12 or 6 containers per carton. Distributed exclusively by: SoupMan Inc. Staten Island, NY 10314
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0530-2015·2014-11-26

    InHarvest Garden Vegetable Seasoning Recalled for Undeclared Milk

    InHarvest, Inc. is recalling Garden Vegetable Seasoning mix because it contains milk, which is not declared on the label.

    Product
    White and Wild Medley/Garden Vegetable 12/36 oz; Product number 10410. Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed Corn Protein, Sun-Dried Tomato, Salt, Autolyzed Yeast Extrac
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0515-2015·2014-11-26

    Welcome Market Toast Recalled for Missing Allergen Statements

    Welcome Market Inc is recalling various varieties of Family Toast due to missing allergen statements for wheat, soy, and/or milk.

    Product
    Family Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0534-2015·2014-11-26

    InHarvest Garden Vegetable Seasoning Mix Recalled for Undeclared Milk

    InHarvest, Inc. is recalling Garden Vegetable Seasoning Mix because it contains milk, which is not declared on the label.

    Product
    Garden Vegetable seasoning Mix 12/4 oz. Product number 141000 Garden Vegetable seasoning mix. 4 oz..; Product number 14000 Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed Cor
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0523-2015·2014-11-26

    Welcome Market Wheat Bran Toast Recalled for Missing Allergen Statements

    Welcome Market Inc is recalling Wheat Bran Toast products because they lack required statements for wheat, soy, and/or milk allergens.

    Product
    Wheat Bran Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0527-2015·2014-11-26

    Formulations For Life Recalls Vision Assure Extra Strength Vision Formula

    Formulations For Life is recalling Vision Assure Extra Strength Vision Formula dietary supplements due to lack of Good Manufacturing Practices and misbranding.

    Product
    FORMULATIONS FOR LIFE Vision Assure Extra Strength Vision Formula DIETARY SUPPLEMENT, 1) 60 VEGETARIAN CAPSULES, 2) 120 VEGETARIAN CAPSULES. Distributed by: Formulations for Life Hauppauge, New York 11788 USA.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0526-2015·2014-11-26

    Formulations For Life Recalls Resevera Action Dietary Supplements for Misbranding

    Formulations For Life is recalling Resevera Action High Potency Longevity Complex dietary supplements due to lack of Good Manufacturing Practices and misbranding.

    Product
    FORMULATIONS FOR LIFE Resevera Action High Potency Longevity Complex DIETARY SUPPLEMENT, 60 VEGETARIAN CAPSULES. Distributed by: Formulations for LIfe Hauppauge, New York 11788 USA.
    Category
    Food
    Distribution
    2 states