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.

6901–6925 of 9611

  • 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
  • LowFDA (Food)·F-0505-2015·2014-11-26

    Masiero Brothers Recalls Lemon Pound Cake for Misbranding

    Masiero Brothers LLC is voluntarily recalling Oven Fresh Lemon Pound Cake due to misbranding. The product was distributed in New York.

    Product
    Oven Fresh Lemon Pound Cake, Net Wt. 5 oz., Oven Fresh Baking, LLC, 70 Clinton Road. Fairfield, NJ 07004, UPC 089595901145
    Category
    Food
    Distribution
    1 state
  • LowFDA (Devices)·Z-0231-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labels list a 5-year expiration instead of 2 years.

    Product
    Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0234-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labeling displays a 5-year expiration instead of the correct 2-year period.

    Product
    Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0230-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date Labeling

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labels list a 5-year expiration date instead of the correct 2-year date.

    Product
    Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0229-2015·2014-11-26

    Siemens Recalls ADVIA Centaur BNP Assay Reagents Due to Labeling Error

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur BNP Assay reagents because approximately 2,000 ReadyPacks contain an incorrect human-readable side label.

    Product
    ADVIA Centaur BNP Assay for in vitro diagnostic use in the quantitative determination of B-type Natriuretic Peptide (BNP) in human plasma using the ADVIA Centaur, Centaur XP, Centaur CP Systems; Catalog Numbers: Cat No. 02816138/SMN 10309044 (100 test) 02816634/SMN 10309045 (50
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0232-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date Labeling

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labeling displays a 5-year expiration period instead of the correct 2-year period.

    Product
    Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0233-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labels list a 5-year expiration date instead of the correct 2-year date.

    Product
    Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0254-2015·2014-11-26

    Hospira Recalls Vancomycin Hydrochloride Vials Due to Mislabeling

    Hospira Inc. is recalling 316,640 vials of Vancomycin Hydrochloride for Injection because product trays were mislabeled to contain a different product.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0491-2015·2014-11-19

    Protein Supplement Recalled for Undeclared Milk Allergen

    Maine Natural Health, Inc. is recalling Fortified Vanilla Dietary Supplement because it fails to declare milk as an allergen.

    Product
    Fortified Vanilla Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0494-2015·2014-11-19

    Rejuvenate Natural Dietary Supplement Recalled for Undeclared Milk Allergen

    Maine Natural Health, Inc. is recalling Rejuvenate Natural Dietary Supplement because it fails to declare the allergen milk.

    Product
    Rejuvenate Natural Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0493-2015·2014-11-19

    Maine Natural Health Recalls Rejuvenate Vanilla Protein Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling Rejuvenate Vanilla Dietary Supplement because it fails to declare the allergen milk. The product was distributed nationwide in 2 lb and 10 oz sizes.

    Product
    Rejuvenate Vanilla Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0486-2015·2014-11-19

    Maine Natural Health Recalls Daily Balance Vanilla Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling Daily Balance Vanilla dietary supplements because they fail to declare the allergen milk. The recall covers 2 lb and 10 oz sizes distributed nationwide.

    Product
    Daily Balance Vanilla Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0487-2015·2014-11-19

    Daily Balance Chocolate Dietary Supplement Recalled for Undeclared Milk Allergen

    Maine Natural Health, Inc. is recalling Daily Balance Chocolate Dietary Supplement because it fails to declare the milk allergen.

    Product
    Daily Balance Chocolate Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0490-2015·2014-11-19

    Protein Supplement Recalled for Failing to Declare Milk Allergen

    Maine Natural Health is recalling Hunger and Weight Chocolate Dietary Supplement because it fails to declare the milk allergen.

    Product
    Hunger and Weight Chocolate Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0476-2015·2014-11-19

    Maine Natural Health Recalls Pure Whey Protein Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling Pure Whey Natural Dietary Supplement because the product fails to declare the allergen milk on the label.

    Product
    Pure Whey Natural Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Packaged in: 2 lb (32 oz), 10 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0489-2015·2014-11-19

    Protein supplement recalled for failing to declare milk allergen

    Maine Natural Health, Inc. is recalling Hunger and Weight Vanilla dietary supplements because they fail to declare the milk allergen.

    Product
    Hunger and Weight Vanilla Dietary Supplement Packaged under the labels Stronger Faster Healthier Whey: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0492-2015·2014-11-19

    Maine Natural Health Recalls Fortified Chocolate Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling fortified chocolate dietary supplements because they fail to declare the allergen milk. The products are sold nationwide in 2 lb and 10 oz sizes.

    Product
    Fortified Chocolate Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0484-2015·2014-11-19

    Maine Natural Health Recalls Coconut Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling Endurance In Race Coconut Dietary Supplement because it fails to declare the allergen milk.

    Product
    Endurance In Race Coconut Dietary Supplement Packaged under the label Stronger Faster Healthier Pack. Packaged in: 2 lb (32 oz), and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0485-2015·2014-11-19

    Maine Natural Health Recalls Endurance In Race Lime Supplement for Undeclared Allergens

    Maine Natural Health, Inc. is recalling Endurance In Race Lime Dietary Supplement because it fails to declare milk and coconut allergens.

    Product
    Endurance In Race Lime Dietary Supplement Packaged under the label Stronger Faster Healthier Pack. Packaged in: 2 lb (32 oz), and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0482-2015·2014-11-19

    Protein supplement recalled for undeclared milk and shellfish allergens

    Maine Natural Health, Inc. is recalling Endurance Pre Race Lime dietary supplement because it fails to declare milk and shellfish allergens.

    Product
    Endurance Pre Race Lime , Dietary Supplement Packaged under the label Stronger Faster Healthier Pack. Packaged in: 2 lb (32 oz), and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0502-2015·2014-11-19

    Mondelez Recalls Chiclets Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Chewing Gum because the label fails to declare soy lecithin, a common allergen.

    Product
    Chiclets Gum, 200 - 2 piece packs (400 pieces), Retail UPC 0 12546 02509 6, Case UPC 10012546108499
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0501-2015·2014-11-19

    Mondelez Recalls Chiclets Fruit Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling specific packages of Chiclets Fruit Flavor Gum because the label fails to declare soy lecithin.

    Product
    1) Chiclets Fruit Flavor Gum, 12 piece, Retail UPC 0 12546 10628 3; 2) Chiclets Fruit Flavor Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02503 4, Case UPC 10012
    Category
    Food
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·080-2014·2014-11-19

    K. Heeps Recalls Pork Sausage Due to Undeclared Soy Allergen

    K. Heeps, Inc. is recalling approximately 2,902 pounds of Bratwurst and Bangers sausage products because they contain undeclared soy lecithin, a known allergen.

    Product
    K. Heeps, Inc. — Pennsylvania Firm Recalls Pork Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0474-2015·2014-11-19

    Maine Natural Health Recalls Pure Whey Vanilla Protein Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling Pure Whey Vanilla dietary supplements because the packaging fails to declare the allergen milk.

    Product
    Pure Whey Vanilla , Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide