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.

6401–6425 of 9611

  • HighFDA (Food)·F-2187-2015·2015-06-10

    Giant Eagle Apricot Filled Cookies Recalled for Undeclared Milk Allergen

    Giant Eagle is recalling Apricot Filled Cookies sold over the counter because the labels failed to declare the milk allergen.

    Product
    Apricot Filled Cookie OTC Sell By: (all dates up to) 3/23/2015 Net WT. 1 OZ Contains:Egg, Wheat, Soy ; Cookies affected are only sold direct from bakery counter and packaged at time per customer request and packed either in clam shell plastic or wax paper. ; Net Weight o
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1637-2015·2015-06-10

    Synovis Recalls Vascu-Guard Patches Due to Surface Identification Issues

    Synovis is recalling specific Vascu-Guard Peripheral Vascular Patch codes because users reported difficulty distinguishing the smooth from the rough surface.

    Product
    Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and product codes: 1x6cm, product code 1504026, 0.8x8cm, product code 1504028, 1x10cm, product code 1504030, and 2x9cm, product code 1504032. VASCU-GUARD is packaged between two pieces of foam within a double st
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2404-2015·2015-06-10

    Giant Eagle Recalls Raisin Filled Cookies for Undeclared Milk Allergen

    Giant Eagle is recalling Raisin Filled Cookies sold over the counter because the labels failed to declare the milk allergen. The recall covers products sold in Maryland, Ohio, Pennsylvania, and West Virginia.

    Product
    Raisin Filled Cookie OTC Sell By: (all dates up to) 3/23/2015 Net WT. 1 OZ Contains:Egg, Wheat, Soy ; OTC Raisin Filled Cookie Sell By: (all dates up to) 3/23/2015 Net WT 2 OZ Contains: Egg, Wheat Soy ; Cookies affected are only sold direct from bakery counter and pac
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2403-2015·2015-06-10

    Ava's Berry Nutty Mix Recalled for Undeclared Sulfites

    Northhampton Peanut Company is recalling Ava's Berry Nutty Mix trail mix because it contains undeclared sulfites.

    Product
    Ava's Berry Nutty Mix trail mix packed in 20 oz. clear plastic containers.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2347-2015·2015-06-10

    Cosmo Creations Salted Caramel Puffed Corn Recalled for Sugar Labeling Error

    4 Him Food Group LLC is recalling Salted Caramel Premium Puffed Corn because the nutrition label incorrectly listed zero grams of sugar per serving.

    Product
    Salted Caramel Premium Puffed Corn, Cosmo Creations brand, Nitrogen filled, 3-layer laminate packaging, Net weight 14 oz., UPC 8 51710 00141 8.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1713-2015·2015-06-10

    Siemens Factor IX Plasma Reagent Recalled for Inaccurate Low-Range Results

    Siemens Healthcare Diagnostics is recalling Factor IX plasma reagents for the BCS/BCS XP system due to erroneously high results at the lower end of the measuring range.

    Product
    Factor deficient plasma for the Siemens BCS¿ / BCS¿ XP System. In vitro diagnostic reagent for the determination of the activity of coagulation factor IX in human plasma by coagulometric methods.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1709-2015·2015-06-10

    AMUSA Recalls 0.9% Sodium Chloride Flush Syringes Due to Incorrect Expiration Date

    MRP, LLC dba AMUSA is recalling 200,000 units of 0.9% Sodium Chloride Injection Flush Syringes because the labels display an incorrect expiration date.

    Product
    0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe.
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1697-2015·2015-06-10

    Coreva Recalls ActCel Hemostatic Dressing for Unapproved Marketing Claims

    Coreva Health Science is recalling ActCel Hemostatic Dressing because customer literature and websites promoted unapproved uses for controlling bleeding in body cavities.

    Product
    ActCel advanced bleeding control Topical Hemostatic Dressing 2in X 2in (5cm X 5cm) 4in X 4in Sterile Contents Soluble Regenerated Cellulose For Bleeding Control For external topical and temporary use only Sterility of contents guaranteed unless individual envelope is d
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Food)·F-2402-2015·2015-06-10

    Roche Brothers Berry Nutty Mix Recalled for Undeclared Sulfites

    Northhampton Peanut Company is recalling Roche Brothers Berry Nutty Mix trail mix because it contains undeclared sulfites, a non-allergen.

    Product
    Roche Brothers Berry Nutty Mix trail mix packed in 9 oz. and 20 oz. clear plastic containers
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-1113-2015·2015-06-10

    Sucrets Cherry Lozenges Recalled for Incorrect Labeling

    Medtech Products is recalling Sucrets Sore Throat & Cough Vapor Cherry lozenges because an incorrect book label was applied to the tins.

    Product
    SUCRETS Sore Throat & Cough Vapor Cherry lozenges, 18-count tin, Dist. By: Insight Pharmaceuticals, LLC, Trevose, PA 19053-8433
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1114-2015·2015-06-10

    Fresenius Kabi Recalls KABIVEN IV Bags Due to Amino Acid Labeling Error

    Fresenius Kabi is recalling 5,488 bags of KABIVEN IV solution because the label lists 3.1% amino acids, but the product actually contains 3.3%.

    Product
    KABIVEN — KABIVEN (DEXTROSE, SOYBEAN OIL, ELECTROLYTES, LYSINE, PHENYLALANINE, LEUCINE, VALINE, THREONINE, METHIONINE, ISOLEUCINE, TRYPTOPHAN, ALANINE, ARGININE, GLYCINE, PROLINE, HISTIDINE, GLUTAMIC ACID, SERINE, ASPARTIC ACID AND TYROSINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1707-2015·2015-06-10

    Ortho-Clinical Diagnostics Recalls VITROS Signal Reagent Due to Labeling Defects

    Ortho-Clinical Diagnostics is recalling VITROS Immunodiagnostic Products Signal Reagent, Lot 3082, because the reagent packs may contain blank labels.

    Product
    VITROS Immunodiagnostic Products Signal Reagent, Product Code 1072693, Unique Device Identifier No. 10758750008360 VITROS Immunodiagnostics Products Signal Reagent (SR) is supplied to users as a sales unit box containing two Signal Reagent Packs. Each Signal Reagent Pack is label
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·088-2015·2015-06-06

    Benedetti Farms Recalls Chicken and Turkey Sausage for Misbranding

    Benedetti Farms is recalling approximately 11,670 pounds of chicken and turkey sausage products because hog and sheep casings were not listed on the labels.

    Product
    Benedetti Farms — Benedetti Farms, Inc. Recalls Chicken and Turkey Sausage Products Due To Misbranding
    Category
    Food
    Distribution
    1 state
  • HighUSDA FSIS·086-2015·2015-06-04

    Demes Gourmet Recalls Chicken Longanisa Due to Unlabeled Hog Casings

    Demes Gourmet Corp. is recalling approximately 29,052 pounds of chicken longanisa because the products were wrapped in hog casings not listed on the labels.

    Product
    Demes Gourmet Corporation — Demes Gourmet Corp. Recalls Chicken and Pork Products Due To Misbranding
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1665-2015·2015-06-03

    United Surgical Associates Recalls Elastic Knee Supports for Missing Latex Label

    United Surgical Associates is recalling 1,260 Elastic Knee Supports because they lack a caution label regarding latex content, posing a risk of allergic skin reactions.

    Product
    Elastic Knee Support. A limb orthosis (brace) is a device intended for medical purposes that is worn on the upper or lower extremities to support, to correct, or to prevent deformities or to align body structures for functional improvement.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-2330-2015·2015-06-03

    EZ's Burger Deluxe Recalled for Undeclared Wheat Allergen

    Regency Group, Inc. is recalling EZ's Burger Deluxe Burger Blend due to undeclared wheat (gluten) contamination.

    Product
    EZ's Burger Deluxe -Burger Blend w/o MSG, stock code 12314, packaged in 50 lbs. container. No UPC.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-2333-2015·2015-06-03

    Fresca Tomato Spice with Beet Recalled for Undeclared Wheat Allergen

    Regency Group is recalling Fresca Tomato Spice with Beet due to gluten contamination and failure to declare wheat on the label.

    Product
    Fresca Tomato Spice with Beet, stock code 12487, packaged in 26 lbs. container. No UPC.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-2336-2015·2015-06-03

    Regency Group Recalls Pizza Seasoning for Undeclared Wheat Allergen

    Regency Group is recalling specific lots of pizza seasoning because the product contains gluten (wheat) but the label does not declare it.

    Product
    Pizza Seasoning, stock code 03388, packaged in 20 lbs. or 50 lbs. container. The UPC is 0 23605 03388 4.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-2332-2015·2015-06-03

    Regency Group Recalls French Fry Seasoning for Undeclared Wheat Allergen

    Regency Group is recalling 200 lbs of French Fry Seasoning because it contains gluten (wheat) but the label does not declare wheat.

    Product
    French Fry Seasoning, stock code 03223, packaged in 50 lbs. container. The UPC is 0 23605 03223 8
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-2338-2015·2015-06-03

    Taco Seasoning Suprema Recalled for Undeclared Wheat Allergen

    Regency Group is recalling Taco Seasoning Suprema because it contains gluten (wheat) but the label does not declare wheat.

    Product
    Taco Seasoning Suprema, stock code 03456, packaged in 1 lb., 5 lbs., 25 lbs., or 50 lbs container. The UPC is 0 23605 03456 0
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-2334-2015·2015-06-03

    James Gang BBQ Bull Breath Chili Seasoning Recalled for Undeclared Wheat

    Regency Group, Inc. is recalling 200 lbs of James Gang BBQ Bull Breath Chili Seasoning because it contains gluten (wheat) but the label does not declare it.

    Product
    James Gang BBQ Bull Breath Chili Seasoning, stock code 11523, packaged in 50 lbs. container. No UPC.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-2337-2015·2015-06-03

    Regency Group Recalls Taco Seasoning No Salt Due to Gluten Contamination

    Regency Group, Inc. is recalling Taco Seasoning No Salt because it is contaminated with gluten (wheat) and the label does not declare wheat.

    Product
    Taco Seasoning No Salt, stock code 03455, packaged in 1 lb., 2 lbs., 3 lbs., or 5 lbs., container. The UPC is 0 23605 03455 3
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1666-2015·2015-06-03

    United Surgical Associates Recalls Keo Wrist Braces for Missing Latex Label

    United Surgical Associates is recalling 756 Keo elastic wrist braces because they lack a caution label regarding latex content, posing a risk of allergic skin reactions.

    Product
    Keo Brace, elastic wrist brace for carpal tunnel. A limb orthosis (brace) is a device intended for medical purposes that is worn on the upper or lower extremities to support, to correct, or to prevent deformities or to align body structures for functional improvement.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1664-2015·2015-06-03

    United Surgical Associates Recalls Elastic Ankle Supports for Missing Latex Label

    United Surgical Associates is recalling 1,278 Elastic Ankle Supports because they lack a caution label regarding latex content, posing a risk of allergic skin reactions.

    Product
    Elastic Ankle Support. A limb orthosis (brace) is a device intended for medical purposes that is worn on the upper or lower extremities to support, to correct, or to prevent deformities or to align body structures for functional improvement.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-2322-2015·2015-06-03

    Gromex Ground Shrimp Recalled for Undeclared Dyes

    Gromex Inc. is recalling 100 lbs of Ground Shrimp found to contain undeclared and unallowed dyes.

    Product
    Gromex Camaron Molido (Ground Shrimp), Net Wt. 2 oz., packaged in a clear bag, Mexican Products, Importers & Distributors, UPC 690912620108
    Category
    Food
    Distribution
    3 states