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.

Which agencies issued them

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.

4951–4975 of 9610

  • ModerateFDA (Devices)·Z-1069-2017·2017-02-01

    Binding Site IgG4 Reagent Kits Recalled for Inaccurate Results

    The Binding Site Group is recalling Human IgG4 Subclass Liquid Reagent Kits because they may yield falsely low results for samples with extremely high IgG4 levels.

    Product
    Human lgG4 Subclass Liquid Reagent Kits For use on the Roche Cobas"6000 This kit is intended for qualifying human IgG subclasses 1,2,3 and 4 immunoglobulins in serum on the Beckman Coulter AU series. Meaurement of these immunoglobulins ais in the diagnosis of abnormal pro
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1104-2017·2017-02-01

    Mesa Laboratories Recalls ProSpore Biological Indicators Due to Reduced Resistance

    Mesa Laboratories is recalling ProSpore 4 mL Ampoule Biological Indicators because product resistance fell outside label claims within the expiration date.

    Product
    ProSpore 4 mL Ampoule Biological indicator for steam sterilization, contains Geobacillus stearothermophilus, Catalog Number: PS-6-50, contains 50 Ampoules/Box. Product Usage: Biological indicator for steam sterilization at 121 deg C intended for use by a health care provide
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Food)·F-1344-2017·2017-02-01

    Dr. Pepper 2-Liter Bottles Recalled for Potential Undeclared Aspartame

    Coca-Cola Consolidated is recalling 2-liter bottles of Dr. Pepper that may contain Diet Dr. Pepper with undeclared aspartame.

    Product
    Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.
    Category
    Food
    Distribution
    1 state
  • LowFDA (Devices)·Z-1105-2017·2017-02-01

    Smiths Medical Recalls NORMFlow H-1100 Irrigation Fluid Warmer for Labeling Errors

    Smiths Medical is recalling one NORMFlow H-1100 Irrigation Fluid Warmer in Sweden due to incorrect Spanish labels instead of English.

    Product
    NORMFlow H-110 Irrigation Fluid Warmer, Continental Europe, Model H-1100, Reorder H-1100-INT-230. Product Usage: NORMOFLO¿ H-1100 Irrigation Fluid Warmers has been designed for safe, in-line warming of irrigating fluids as they are administered to patients. The Fluid Warmer
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·17079·2017-01-31

    Teufelberger Recalls Static Ropes and Throwlines Due to Fall Hazards

    Teufelberger is recalling specific static ropes and throwlines because they are mislabeled as certified to NFPA safety standards, posing fall and injury risks to users.

    Product
    Static ropes and throwlines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V060000·2017-01-26

    Forest River Recalls 2017 XLR Fifth-Wheel RVs for Incorrect Placard

    Forest River is recalling 2017 XLR fifth-wheel recreational vehicles because the Federal Placard incorrectly identifies them as Travel Trailers, which may lead to improper towing and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1283-2017·2017-01-25

    Bakers of Paris Croissants Recalled for Undeclared Egg Allergen

    Bakers of Paris is recalling croissants sold in Northern California because the labels fail to declare egg, a major allergen, despite the product containing an egg wash.

    Product
    Croissant:: sold in self serve cases and 4 pack clamshell package. Ingredients: Dough (enriched unbleached flour [wheat flour, malted barley flour, niacin, iron, thiamin, mononitrate, riboflavin, folic acid] water, butter, sugar, milk, yeast, salt, ascorbic acid, enzymes. Toppin
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1286-2017·2017-01-25

    Bakers of Paris Croissants Recalled for Undeclared Egg Allergen

    Bakers of Paris is recalling assorted croissants sold in Northern California because the packaging fails to declare egg, a major allergen, in the ingredients list.

    Product
    Assorted Croissant:: sold in 4 pack clamshell package. Ingredients: Plain Croissant: ( dough [enriched unbleached flour (wheat flour, malted barley flour, niacin, iron, thiamin, mononitrate, riboflavin, folic acid) water, butter, sugar, milk, yeast, salt, ascorbic acid, enzymes}
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1285-2017·2017-01-25

    Bakers of Paris Almond Croissants Recalled for Undeclared Egg Allergen

    Bakers of Paris is recalling Almond Croissants sold in Northern California because the labels failed to declare egg, a major allergen.

    Product
    Almond Croissant:: sold in self serve cases and 4 pack clamshell package. Ingredients: Dough ( water, wheat flour, sugar, milk [powder fat whole], salt, yeast, ascorbic acid, butter. Filling: Almond paste, butter, sugar, eggs. Topping (apricot glaze, almonds. Contains Milk, Egg
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1275-2017·2017-01-25

    Hungry Heart Cracker Jax Recalled for Undeclared Milk and Soy Allergens

    Hungry Heart Bakery is recalling Cracker Jax because the product contains milk and soy that are not declared on the label.

    Product
    Cracker Jax, Hungry Heart brand, packaged in a clear Cello bag, heat sealed. Net wt. 8 oz. (227g).
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1284-2017·2017-01-25

    Bakers of Paris Chocolate Croissants Recalled for Undeclared Egg Allergen

    Bakers of Paris is recalling 645 chocolate croissants sold in Northern California because the labels fail to declare egg, a major allergen.

    Product
    Chocolate Croissant:: sold in self serve cases and 4 pack clamshell package. Ingredients: Dough (enriched unbleached flour [wheat flour, malted barley flour, niacin, iron, thiamin, mononitrate, riboflavin, folic acid] water, butter, sugar, milk, yeast, salt, ascorbic acid, enzym
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1259-2017·2017-01-25

    NY Rye Deli Loaf Recalled for Undeclared Soy Allergen

    Great Northern Bakehouse is recalling NY Rye Deli Loaves because they contain undeclared soy lecithin from a pan spray.

    Product
    NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1025-2017·2017-01-25

    Zimmer Biomet Recalls ArComXL Polyethylene Bearings Due to Labeling Mismatch

    Zimmer Biomet is recalling 19 ArComXL Polyethylene Bearings because packaging labels did not match the physical product inside, posing a risk of surgical delay.

    Product
    Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-200152
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1330-2017·2017-01-25

    O'Pelle Bakery Egg Bagels Recalled for Missing Yellow 5 Labeling

    O'Pelle Enterprises is recalling frozen raw Egg Bagels because the label fails to declare Yellow 5, a common food dye.

    Product
    Opelle Bakery Egg Bagel (C-105), case of 60 (3.5 oz.), Frozen Raw.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1024-2017·2017-01-25

    Zimmer Biomet Recalls ArComXL Polyethylene Liners Due to Labeling Mismatch

    Zimmer Biomet is recalling 36 units of ArComXL polyethylene liners because packaging labels did not match the physical product, posing a risk of surgical delay.

    Product
    RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1032-2017·2017-01-25

    Exactech Recalls Alteon Neck Preserving Stems Due to Incorrect GTIN Labels

    Exactech is recalling 98 Alteon Neck Preserving Stems because they were labeled with incorrect Global Trade Item Numbers (GTINs) that identify them as different devices.

    Product
    Alteon Neck Preserving Stem, Standard Offset, Plasma Coated, Size 6
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-1031-2017·2017-01-25

    Exactech Recalls Polyethylene Acetabular Liners Due to Incorrect GTIN Labels

    Exactech, Inc. is recalling 12 polyethylene acetabular liners because they were labeled with incorrect Global Trade Item Numbers (GTINs).

    Product
    AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-1038-2017·2017-01-25

    Endologix AFX Endovascular AAA System Instructions for Use Update

    Endologix updated the Instructions for Use for the AFX Endovascular AAA System to address endoleak Type IIIB.

    Product
    AFX Endovascular AAA System, Endoleak Type IIIB; The AFX Endovascular AAA System is intended for endovascular treatment of patients with abdominal aortic or aortoiliac aneurysms (AAA).
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-1331-2017·2017-01-25

    O'Pelle Bakery Egg Bagels Recalled for Missing Yellow 5 Labeling

    O'Pelle Enterprises is recalling frozen raw Egg Bagels because the label fails to declare Yellow 5. The product was distributed only within Florida.

    Product
    Opelle Bakery Egg Bagel (B-105), case of 96 (4 oz.), Frozen Raw.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1030-2017·2017-01-25

    Exactech Recalls Novation Cemented Plus Femoral Stems Due to Labeling Error

    Exactech is recalling 79 Novation Cemented Plus Femoral Stems because they were labeled with incorrect Global Trade Item Numbers (GTINs).

    Product
    Novation Cemented Plus Femoral Stem, 12/14, Collared, Standard Offset, Matte, Cemented, Size 15.
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Food)·F-1093-2017·2017-01-18

    Piazza Produce Recalls Fajita Seasoning for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling specific lots of Fajita seasoning because the product labeling does not list ingredients, including undeclared soybean oil.

    Product
    Fajita seasoning, 9 lb plastic gallon, product number 63545; Fajita seasoning, 2.5 lb plastic jar, product number 63543
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1109-2017·2017-01-18

    Piazza Produce Salt Free Vegetable Herb Recalled for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling Salt Free Vegetable Herb products because the labels do not list ingredients, including undeclared soybean oil.

    Product
    Salt Free Vegetable Herb, 5.5 lb plastic gallon, product number 63524; Salt Free Vegetable Herb, 1.5 lb plastic jar, product number 63522
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1006-2017·2017-01-18

    Philips IQon Spectral CT Recalled for Image and Scan Errors

    Philips is recalling 35 IQon Spectral CT systems due to software issues causing rescans, incorrect scan locations, or misrepresentation of image results.

    Product
    IQon Spectral CT with software version 4.7.0 Product Usage: The IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This devic
    Category
    Medical Device
    Distribution
    Distributed nationwide