The Recall Desk

Hazard

Mis Labeling recalls

9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,606
Critical
160
Severe
588
Most recent
2026-09-09

Of the 9,606 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.

501–525 of 9606

  • HighFDA (Food)·F-1132-2024·2024-04-17

    Egg Salad Sandwich Recalled for Undeclared Fish Allergen Mislabeling

    Tuna salad sandwiches were mislabeled as egg salad, creating an undeclared fish allergen risk for consumers. The recall affects 551 units distributed to institutions and retailers across ten states.

    Product
    Egg salad sandwich packaged in clamshell for individual sale. 7.22oz (205g) UPC 766375938415
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-1141-2024·2024-04-17

    Peach pie recalled for missing sub-ingredient information

    Robeson Enterprises is recalling Peach Pie distributed to GA, NC, and SC because the label fails to list sub-ingredients. The recall affects all lots shipped before February 23, 2024.

    Product
    PIES & SIDES PEACH PIE INGREDIENTS: PEACH PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1137-2024·2024-04-17

    Green Bean Casserole Missing Ingredient Label for Common Allergens

    Green Bean Casserole recalled by Robeson Enterprises due to missing ingredient labels. Product contains undeclared milk, soy, fish, and wheat allergens.

    Product
    PIES & SIDES GREEN BEAN CASSEROLE, CONTAINS: MILK, SOY, FISH, WHEAT, PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1134-2024·2024-04-17

    Cherry Pie Recalled for Missing Sub-Ingredient Label Information

    Robeson Enterprises is recalling cherry pie products because labels do not list sub-ingredients. Products were distributed in Georgia, North Carolina, and South Carolina.

    Product
    PIES & SIDES CHERRY PIE INGREDIENTS: CHERRY PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR SPICES. CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1146-2024·2024-04-17

    Sweet Potato Casserole Recall Due to Missing Ingredient Labels

    Robeson Enterprises is recalling Pies & Sides Sweet Potato Casserole because the product label fails to list any ingredients, including egg and milk. Consumers with allergies to these ingredients should not consume the product.

    Product
    PIES & SIDES SWEET POTATO CASSEROLE CONTAINS: EGG, MILK PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1135-2024·2024-04-17

    Caramel Apple Pie Recalled for Missing Sub-Ingredient Labels

    Robeson Enterprises is recalling 2,984 units of Pies & Sides Connie's Caramel Apple Pie due to incomplete ingredient labeling. The product labels do not list sub-ingredients for prepared components.

    Product
    PIES & SIDES CONNIE'S CARAMEL APPLE PIE 11 oz INGREDIENTS: APPLE PIE FILLING, SUGARS, VANILLA, CARAMEL EXTRACT BLEACHED FLOUR, SPICES, CONTAINS: WHEAT, PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1456-2024·2024-04-10

    ATTUNE AFFIXIUM Knee Implant Component Recalled for Incorrect Labeling

    DePuy Orthopaedics is recalling ATTUNE AFFIXIUM Cementless Fixed Bearing Knee implants (Size 6) due to incorrect labeling. The affected product includes Model No. 150621006 with Lot JA06A0252.

    Product
    ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Component of the ATTUNE Total Knee Replacement System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1110-2024·2024-04-10

    Hood Country Style Cottage Cheese Recalled for Undeclared Ingredients

    HP Hood is recalling Country Style Cottage Cheese 24oz due to undeclared pineapple and other ingredients. Consumers with pineapple allergies or sensitivity to listed ingredients should not consume the product.

    Product
    Hood Country Style Cottage Cheese 24oz (UPC 044100106385),
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0434-2024·2024-04-10

    Cyclophosphamide Injection Recalled for Package Insert Concentration Labeling Error

    X-Gen Pharmaceuticals recalls Cyclophosphamide for Injection due to a labeling error in the Package Insert. Section 2.3 incorrectly lists the concentration as '20 mg per vial' instead of the correct '20 mg per mL'.

    Product
    Cyclophosphamide for Injection, USP, 1g/vial, Lyophilized, Single Dose Vial, Discard unused solution, Cytotoxic Agent, After Reconstitution: For direct intravenous injection or must be further diluted before intravenous infusion, Rx Only, Manufactured for: XGen Pharmaceuticals DJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0433-2024·2024-04-10

    Cyclophosphamide Injection Recalled for Package Insert Concentration Labeling Error

    X-Gen Pharmaceuticals is recalling 1,283 vials of Cyclophosphamide for Injection due to a Package Insert error that lists concentration as '20 mg per vial' instead of '20 mg per mL'. No illnesses have been reported.

    Product
    Cyclophosphamide for Injection, USP, 500mg/vial, Lyophilized, Cytotoxic Agent, Single Dose Vial for Intravenous Use, Rx Only, Manufactured for: XGen Pharmaceuticals DJB, Inc. Big Flats, NY 14814, NDC # 39822-0250-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1461-2024·2024-04-10

    Halyard surgical hood mislabeled as surgical cap at dispenser

    O&M Halyard is recalling approximately 75,000 surgical hoods mislabeled as surgical caps at the dispenser level.

    Product
    HALYARD SURGICAL HOOD, Universal Size, Blue, 300 count (3 x 100)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1391-2024·2024-04-03

    Puritan HydroFlock Collection Device Distributed with Wrong Product Code

    Puritan Medical Products distributed HydroFlock Sterile Flocked Collection Devices labeled as Part Number 25-3317-H, Lot S1014 that actually contain product code 25-3317-U. Approximately 232,500 units were affected.

    Product
    HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1102-2024·2024-04-03

    Sunflour Bakery Marzipan Coffee Cake Recalled for Undeclared Yellow #5

    NRS Enterprises, Inc. dba Sunflour Bakery is recalling Marzipan/Almond Coffee Cake because Yellow #5 was not declared on the label. The product was distributed in California.

    Product
    Marzipan/Almond Coffee Cake, 16 oz, in clear poly bags
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1104-2024·2024-04-03

    FDA Recalls German Home Bakery Cherry Coffee Cake for Undeclared Yellow #5

    NRS Enterprises, Inc. is recalling German Home Bakery Cherry Coffee Cake due to undeclared Yellow #5. The product was distributed in California and may affect consumers with tartrazine sensitivity.

    Product
    German Home Bakery Cherry Coffee Cake, 16 oz, clear poly bag
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·F-1095-2024·2024-04-03

    Juice Recall: Incorrect SKU Label on Golden Sunrise Cold Pressed Juice

    Pressery, LLC is recalling Golden Sunrise Cold Pressured Juice due to an incorrect SKU label. No illnesses or injuries have been reported.

    Product
    The label reads, "Golden Sunrise Cold Pressured Juice Carrot, Orange, Pineapple, Lemon, Ginger & Turmeric 11 fl. oz."
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1083-2024·2024-03-27

    Vegan Pecan Oat Scones Recalled for Undeclared Wheat Allergen

    Ethos Bakery is recalling Vegan Pecan Oat Scones distributed in Washington because the product label fails to declare wheat as an allergen, despite wheat flour being present in the product.

    Product
    Vegan Pecan Oat Scone; 4 oz/plastic sleeve; The label of recalled product is read in parts: [Ingredients: Granulated sugar, Wheat flour, Vegan butter (refined coconut oil, soy milk, vegetable oil, soy lecithin,) Sonoran wheat flour, Water, Egg replacer (potato starch, tapioca
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1084-2024·2024-03-27

    Ethos Bakery Vegan Snickerdoodles Recalled for Undeclared Wheat Allergen

    Ethos Bakery is recalling 4 oz packages of Vegan Snickerdoodles distributed in Washington because the labels do not clearly specify that wheat flour is present, creating a risk for consumers with wheat allergies.

    Product
    Vegan Snickerdoodle; 4 oz/plastic sleeve; The label of recalled product is read in parts: ***Vegan Snickerdoodle ***[Ingredients: Granulated sugar, Wheat flour, Vegan butter (refined coconut oil, soy milk, vegetable oil, soy lecithin,) Sonoran wheat flour, Water, Egg replacer (
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1316-2024·2024-03-27

    Medtronic DLP Vessel Cannula Recalled for Incorrect Labeling

    Medtronic is recalling 4,343 units of DLP Vessel Cannula (Model REF 30000) due to incorrect labeling on three manufactured lots distributed globally.

    Product
    Medtronic DLP Vessel Cannula, Model Number REF 30000
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-1055-2024·2024-03-20

    CK Turkey and Cheese Sandwich recalled for undeclared sesame allergen

    CK Turkey and Cheese Sandwich is recalled for undeclared sesame allergen. The sandwich label lists only Wheat, Milk, and Soy allergens, missing sesame which poses risk to allergic consumers.

    Product
    CK Turkey and Cheese Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready to eat product. UPC 983644000141. The sandwich label declares "Ingredients: Multigrain Bread ***Contains: Wheat, Milk, Soy."
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1066-2024·2024-03-20

    KALO Carrot Cake mislabeled with Chocolate Cake ingredients, soy allergen undisclosed

    KALO Carrot Cake All Natural Gluten Free is mislabeled with Chocolate Cake ingredient information that omits soy, creating an allergen hazard for consumers with soy allergy.

    Product
    KALO Carrot Cake All Natural Gluten Free Serving size one slice (6 oz/177g) CONTAINS MILK, EGG UPC 8 53407 00418 4 Distributed by: Kalo Foods, LLC Stokesdale, NC 27357
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1067-2024·2024-03-20

    KALO Chocolate Cake Recalled Due to Undeclared Soy Allergen

    KALO Chocolate Cake packages contain carrot cake with undeclared soy not listed on the label. Consumers with soy allergies are at risk of allergic reaction.

    Product
    KALO Chocolate Cake All Natural Gluten Free Serving size one slice (6 oz/177g) CONTAINS MILK, EGG UPC 8 53407 00418 4 Distributed by: Kalo Foods, LLC Stokesdale, NC 27357
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1298-2024·2024-03-20

    Hip prosthesis labeling clarification needed to prevent surgical confusion

    Waldemar Link is clarifying labeling on 153 hip prosthesis units after complaints about ambiguous Size and Type information. The guidance aims to prevent potential misinterpretation during surgery.

    Product
    SPII Model Lubinus, Long Stem Prosthesis Standard Neck, cemented
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1064-2024·2024-03-20

    Electric City Sweets Chocolate Bars Recalled for Undeclared Milk

    Electric City Sweets 1.75oz Red Velvet Milk Chocolate Bars are being recalled because milk is not properly declared on the packaging. The recall affects 1,644 bars distributed in California, Florida, Pennsylvania, and North Carolina.

    Product
    Electric City Sweets 1.75oz Red Velvet Milk Chocolate Bar. Individually wrapped in paper/foil packaging.
    Category
    Food
    Distribution
    4 states
  • HighNHTSA·24V209000·2024-03-19

    2024 Alfa Romeo Tonale vehicles with missing tire and rim label information

    Chrysler is recalling certain 2024 Alfa Romeo Tonale vehicles because the manufacturer label is missing tire rim and tire size information, which could lead to incorrect wheel installation and increase crash risk.

    Product
    DODGE — DODGE, ALFA ROMEO HORNET, TONALE PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide