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.

201–225 of 9606

  • ModerateFDA (Devices)·Z-1645-2025·2025-04-30

    Zimmer Biomet Ceramic Hip Prosthesis Head Lacks Stem Compatibility Information

    Zimmer, Inc. is recalling a ceramic hip prosthesis head because its labeling does not adequately describe compatibility with cobalt-chrome or stainless-steel femoral stems.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +0 Neck, Model Number 802602202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1647-2025·2025-04-30

    Zimmer Biomet Ceramic Hip Prosthesis Heads Lack Stem Compatibility Information

    Zimmer, Inc. is recalling Zimmer Biomet Ceramic Head hip prostheses (Model 802802201, 22.2 mm diameter) because product labeling does not adequately provide compatibility information for use with cobalt-chrome or stainless-steel femoral stems.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, -3 Neck, Model Number 802802201; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1658-2025·2025-04-30

    Edge Biologicals Sterile Water incorrectly labeled product packaging

    Edge Biologicals is recalling Sterile Water, 3mL (Product Number T-0780, Lot 01223) due to incorrect labeling on the product's outer packaging. The affected units were distributed nationwide in Pennsylvania.

    Product
    Edge Biologicals STERILE WATER, 3ML, 100/PK CAT T-0780 Sterile Water, 3mL, 10/PK - Sterile water is used in making dilutions of samples/transport media in preparation for microbial testing of the sample. It is also used for diluting sterile reagents and microorganism preparat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0707-2025·2025-04-23

    Falafel King Hummus Recalled for Undeclared Sesame Allergen

    Falafel King Enterprises is recalling Traditional Hummus in 13 oz multi-component containers because the label declares tahini paste but fails to declare sesame, a common allergen.

    Product
    Falafel King Taste the Mediterranean is a multi-component, 4 section plastic container, that includes Traditional Hummus, Falafel Balls, Tzatziki, and Mixed Vegetables. " Net Wt: 13 oz. UPC 82298621035 4. The Traditional Hummus is the recalled product and the ingredient statemen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1569-2025·2025-04-23

    Conformis Restor3d Cordera Hip Acetabular Liner Mislabeled

    Conformis is recalling certain Cordera Hip acetabular liners from Lot 1788258 due to incorrect labeling. Units labeled as standard liners actually contain hooded liners, creating a mismatch between the label and the product.

    Product
    restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Model Number: HDL-060-C22L-000101 Acetabular Liner for Cordera Hip System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0717-2025·2025-04-23

    Golden Crop Candy contains undeclared food color additives

    Blooming Import Inc. is recalling Golden Crop Candy (8 oz unwrapped) due to undeclared and unallowed color additives: Blue 1, Red 40, and Acid Red 18.

    Product
    Golden Crop Candy (8 oz. (227g) un-wrapped candies)
    Category
    Food
    Distribution
    8 states
  • ModerateNHTSA·25V271000·2025-04-23

    Ford Recalls 2025 F-150 Vehicles for Missing Air Bag Warning Labels

    Ford is recalling 2025 F-150 vehicles because the air bag warning label may be missing from the dashboard, failing to comply with federal safety standards.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0715-2025·2025-04-23

    Tortilla Chips Recalled Due to Undeclared Yellow #5 Dye

    La Mexicana Tortilla Factory is recalling Tortilla Chip Green 4 cut products due to undeclared Yellow #5, an FDA-certified colorant that poses a risk to consumers with dye sensitivities or allergies.

    Product
    Tortilla Chip Green 4 cut packed 5lbs per bag; 6 bags per box
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0716-2025·2025-04-23

    Golden Crop Candy Recalled for Undeclared Food Color Additives

    Blooming Import Inc. is recalling Golden Crop Candy (10 oz. wrapped candies) because it contains undeclared and unallowed food color additives: Blue 1, Red 40, and Acid Red 18.

    Product
    Golden Crop Candy (10 oz. (283g) wrapped candies)
    Category
    Food
    Distribution
    8 states
  • LowFDA (Food)·F-0705-2025·2025-04-23

    Dried Seedless Plum Candy Recalled Due to Undeclared Cyclamates

    BaiWei ShanZhuang Dried Seedless Plum Candy is being recalled because it contains cyclamates, which are not declared on the label. The product was distributed across multiple states.

    Product
    BaiWei ShanZhuang, Dried Seedless Plum Candy, 9.16 oz. (260g), plastic bags, 30 bags per case.
    Category
    Food
    Distribution
    11 states
  • HighNHTSA·25V265000·2025-04-21

    Highland Ridge Recalls 2025 GO Play Travel Trailers for Label Errors

    Highland Ridge RV is recalling 2025 GO Play travel trailers because incorrect weight and tire labels may lead to overloading and crashes.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT GO PLAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0699-2025·2025-04-16

    Lillie's Q Buffalo Wing Sauce recalled for undeclared milk allergen

    OLD WORLD SPICES & SEASONING, INC is recalling Lillie's Q Buffalo Wing Sauce (13.5 oz bottles, Lot #002125 and others) because milk, present as a sub-ingredient in butter, is not declared on the label or in the "Contains" statement.

    Product
    Lillie's Q Buffalo Wing Sauce. Net wt. 13.5 oz, UPC 810069510972, Case label: Lillie's Q Buffalo Wing Sauce, Item # FGLOL422 Lot # 002125, 6/13.5 oz, UPC 10810069510979, BEST BY: JAN/21/2026
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-0698-2025·2025-04-16

    MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement recall undeclared soy

    MTN OPS, LLC is recalling MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement (60 capsule bottles) because they contain undeclared soy flour, which poses a risk to consumers with soy allergies.

    Product
    MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement, 60 Capsule Bottle (30 Serving). Manufactured exclusively for MTN OPS, LLC, 251 S Mountain Rd., Fruit Heights, UT. UPC 8 40359 40458 2
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0718-2025·2025-04-16

    Dried Cranberries Recalled for Incorrect Carbohydrate Labeling

    Victor Packing Inc. is recalling dried cranberries because the label lists 2g total carbohydrates instead of the correct 27g. The mislabeling affects 34,500 cases distributed across multiple states.

    Product
    Dried Cranberries (21.75 lb/case; 300 - 1.16 oz packages/case)
    Category
    Food
    Distribution
    9 states
  • HighNHTSA·25T006000·2025-04-15

    Goodyear Recalls Cooper Tires Missing Identification Codes

    Goodyear is recalling specific Cooper Discoverer Stronghold AT tires because they lack the required week and year code. This prevents owners from determining the tire's age or recall status.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0676-2025·2025-04-09

    Choshiya Aokappa Zuke Prepared Mix Vegetables Recalled for Missing Refrigeration Label

    AKT Trading Inc. is recalling Choshiya branded Aokappa Zuke Prepared Mix Vegetables because the product label lacks a 'Keep Refrigerated' statement, risking improper storage of non-shelf-stable vegetables.

    Product
    Choshiya branded "AOKAPPA ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535135
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0678-2025·2025-04-09

    Packaged Vegetables Recalled for Missing Refrigeration Label Statement

    AKT Trading Inc. is recalling Choshiya branded Soft Tsubozuke Prepared Mix Vegetables due to missing "Keep Refrigerated" statement on labels. Non-shelf stable vegetables lacking this statement may spoil or develop harmful bacteria if stored improperly.

    Product
    Choshiya branded "SOFT TSUBOZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535159
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0680-2025·2025-04-09

    Choshiya Prepared Bamboo Shoots Recalled Due to Missing Keep Refrigerated Label

    Choshiya branded menma (prepared bamboo shoots) are being recalled because the label fails to include the required 'Keep Refrigerated' statement. Improper storage of this non-shelf-stable product could lead to foodborne illness.

    Product
    Choshiya branded "MENMA AJITSUKE PREPARED BAMBOO SHOOTS" UPC# JANCODE 4983673527325
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0677-2025·2025-04-09

    Choshiya Prepared Vegetables Recalled for Missing Refrigeration Label

    AKT Trading Inc. is recalling Choshiya branded Fukushin Zuke Prepared Mix Vegetables due to a labeling deficiency. The non-shelf-stable product is missing the required "Keep Refrigerated" statement.

    Product
    Choshiya branded "FUKUSHIN ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535142
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0675-2025·2025-04-09

    Choshiya Shiba Zuke Prepared Mix Vegetables Recalled for Missing Refrigeration Label

    AKT Trading Inc. is recalling Choshiya branded Shiba Zuke Prepared Mix Vegetables (1,000 cases) because they are missing the required "Keep Refrigerated" statement on the label. Non-shelf stable vegetables could be improperly stored without this critical labeling information.

    Product
    Choshiya branded "SHIBA ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535128
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0679-2025·2025-04-09

    Choshiya Rakkyo Zuke Prepared Vegetables Recalled for Missing Refrigeration Label

    Choshiya brand rakkyo zuke prepared vegetables are being recalled due to missing 'Keep Refrigerated' label statements. These non-shelf-stable vegetables may spoil if not properly refrigerated.

    Product
    Choshiya branded "RAKKYO ZUKE PREPARED VEGETABLES" UPC# JANCODE 4983673526021
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0686-2025·2025-04-09

    Turkey BLT Sandwiches Recalled for Undeclared Peanut Allergen

    The Coastal Companies is recalling Turkey BLT on Sourdough sandwiches because some packages contain incorrectly labeled Peanut Butter & Jelly sandwiches instead, exposing consumers to an undeclared peanut allergen.

    Product
    Turkey BLT on Sourdough Net Wt. 8.94 OZ (253g) in plastic clamshell
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0692-2025·2025-04-09

    Panang Curry Tofu Vegan GF recalled for undeclared soy allergen

    Seattle Homemade Thai LLC is recalling Panang Curry Tofu Vegan GF because the label declares tofu but does not declare soy as an allergen, creating risk for consumers with soy allergies.

    Product
    Panang Curry Tofu Vegan GF is a refrigerated and ready to eat product, packaged in plastic box, net wt. 13.5oz. UPC 88581 149928. Label declares ingredients as Tofu, Panang Curry Paste, Carrots and Peas, Coconut Milk, Kaffir Lime Leaves.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1502-2025·2025-04-09

    Diagnostic reagent recalls incorrect ISI value on Pacific Hemostasis Thromboplastin-D

    Fisher Diagnostics is recalling Pacific Hemostasis Thromboplastin-D due to an incorrect International Sensitivity Index (ISI) value printed on the outer box label. The error could affect interpretation of prothrombin time test results.

    Product
    Pacific Hemostasis Thromboplastin-D, 4 ml. Used in performing one-stage prothrombin time test and factor assays.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0666-2025·2025-04-02

    Our Family Traverse City Cherry Ground Coffee Recalled for Mislabeling

    Our Family Traverse City Cherry Ground Coffee (12 oz) has been recalled due to mislabeling. A portion of production was labeled as decaffeinated when it contains regular caffeine.

    Product
    COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ (340g) UPC 0 70253 11080 1 DISTRIBUTED BY THE SPARTANNASH COMPANY GRAND RAPIDS, MI 49518
    Category
    Food
    Distribution
    15 states