The Recall Desk

Hazard

Mis Labeling recalls

1,381 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

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.

251–275 of 1381

  • HighFDA (Food)·H-0012-2025·2025-06-11

    Dr. Pepper Zero Sugar Recalled: Mislabeled Cans Contain Full Sugar

    Dr. Pepper Zero Sugar beverages sold in Florida, Georgia, and South Carolina are recalled because cans labeled 'Zero Sugar' actually contain full-sugar product. Consumers should discontinue use immediately.

    Product
    Dr. Pepper, ZERO SUGAR, 12 FL OZ (355 mL) ALUMINUM CAN packaged and sold as 12 packs and 24 packs cartons cases. PRODUCED UNDER THE AUTHORITY OF CB Manufacturing Company, Inc., 5829 Pepsi Pl., Jacksonville, Florida, United States of America, 32216 - 904-443-0763 who is licensed t
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1890-2025·2025-06-11

    FoundationOne Companion Diagnostic Reports Contain Incorrect Claims

    Two FoundationOne Companion Diagnostic reports contained incorrect negative claims on the claims page, though tumor profiling data displayed correctly. No patient harm reported.

    Product
    FoundationOne Companion Diagnostic (F1CDx)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0840-2025·2025-06-11

    Nordic Naturals Kids Multivitamin Gummies Recalled Due to Mislabeling

    Nordic Naturals is recalling 1,164 bottles of its Zero Sugar Kids Multivitamin Supplement Gummies (Lot 244423) because the product is mislabeled.

    Product
    Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case
    Category
    Drug
    Distribution
    20 states
  • HighFDA (Devices)·Z-1876-2025·2025-06-04

    VITROS Chemistry CRP Slides Recalled for Incorrect Generation Labeling

    VITROS Chemistry CRP Slides were labeled with incorrect generation designation (GEN 88 instead of GEN 83). This labeling error could lead to improper device usage and diagnostic errors.

    Product
    VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges, of 18 slides per cartridge, for a total of 90 slides.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1861-2025·2025-06-04

    Straumann Plus Initial Drill Recalled for Missing Laser Engraving

    Straumann USA is recalling 288 units of Plus Initial Drill due to missing laser engraving on the 7 mm component. The defect may affect product identification.

    Product
    Plus Initial Drill, Article Number: 103.170;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0806-2025·2025-05-28

    Yellowstone Baked Beans Recalled for Undeclared Soy Allergen

    Yellowstone Brown Sugar Molasses Baked Beans are being recalled due to mislabeling. The product is labeled as Brown Sugar Molasses Baked Beans but actually contains Beef and BBQ Baked Beans with undeclared soy.

    Product
    Yellowstone Brown Sugar Molasses Baked Beans, NET WT. 15 OZ (425g), packaged in cans, packed 12 cans per case. UPC: 071846187071; Packaged by: Vietti Foods Inc. Nashville, TN 37203
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·F-0770-2025·2025-05-21

    Yogurt Parfait Recalled for Undeclared Almond Allergen

    Knockroe Inc has recalled Bonya Pineapple Yogurt Parfait products containing undeclared almonds. The recall affects 3,912 units distributed to New York, Pennsylvania, Massachusetts, and New Jersey.

    Product
    Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0763-2025·2025-05-21

    Yogurt Parfait Recalled for Undeclared Almond Allergen

    Knockroe Inc recalls Bonya Strawberry Yogurt Parfait due to undeclared almonds. The product was distributed to NY, PA, MA, and NJ; consumers with almond allergies should not consume it.

    Product
    Bonya Strawberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1754-2025·2025-05-21

    BIB Balloon in Balloon Dilatation Catheter Recall Due to Swapped Labels

    Numed Inc is recalling BIB Balloon in Balloon Dilatation Catheter Model 420 due to incorrect labeling of balloon extension lumens. The inner and outer balloon inflation hubs are labeled backwards, creating risk of incorrect balloon inflation during procedures.

    Product
    BIB Balloon in Balloon Dilatation Catheter. Model Number: 420
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0802-2025·2025-05-21

    Beijing Soybean Paste recalled for undeclared wheat allergen

    May Flower International Inc is recalling Beijing Soybean Paste due to undeclared wheat. The product may cause allergic reactions in consumers with wheat sensitivities.

    Product
    Beijing Soybean Paste, packaged in 8.82 ounce/250g red and white packages; Ingredients Soybean, Flour, Salt, Water, Potassium Sorbate; UPC: 6917799000385
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-1691-2025·2025-05-07

    Automated External Defibrillators Model DDU-2200 Missing Required Italian Language Instructions

    Defibtech Automated External Defibrillators (Model DDU-2200) distributed in Switzerland lack Italian language instructions, violating Swiss Medical Devices Ordinance requirements for three-language labeling.

    Product
    Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual language), DCF-E2210-F3/1¿(French/English dual language)
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-1690-2025·2025-05-07

    Semi-automated external defibrillators lack required Italian language instructions

    Defibtech semi-automated external defibrillators distributed to Switzerland lack required Italian translations of product information and instructions for use, violating Swiss Medical Devices Ordinance requirements for multilingual labeling.

    Product
    Semi-Automated External Defibrillators; Models: DDU-100 and DDU-100E. Item numbers: DCF-E110SG-DE/1 (German language), DCF-E110SG-FR/1 (French language), DCF-E110SG-IT/1 (Italian language)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1671-2025·2025-04-30

    Dental Implant Abutments Recalled for Incorrect Blister Labelling

    Straumann USA LLC is recalling WB XL Anatomic Healing Abutment XC dental implant abutments worldwide due to incorrect blister labelling that could compromise product identification.

    Product
    WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1647-2025·2025-04-30

    Zimmer Biomet Hip Prosthesis Ceramic Head Lacks Compatibility Information

    Zimmer, Inc. is recalling ceramic hip prosthesis heads (22.2 mm diameter) because product labeling does not adequately specify compatibility 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
  • HighFDA (Food)·F-0710-2025·2025-04-23

    Panaderia Salvadorena Quesadilla de Queso recalled for undeclared milk

    Panaderia Salvadorena Ii is recalling Quesadilla de Queso products for undeclared milk content. Affected products distributed in Massachusetts and Rhode Island may pose a risk to consumers with milk allergies.

    Product
    PANADERIA/BAKERY Salvadorena; Quesadilla de Queso; Ingredients: Rice, Wheat Flour, soy, eggs, sugar, butter, baking powder, salt, water, sour cream, sesame seeds; UPC 0 21651 16499 6; NET WEIGHT APPROX 14 OZ
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0708-2025·2025-04-23

    Arepas de Chocolo recalled due to undeclared soy allergen

    Delicias de la Abuela Inc is recalling Arepas de Chocolo due to undeclared soy lecithin. The product poses a health risk to consumers with soy allergies.

    Product
    Arepas de Chocolo, Abuelas Food Company, Delicias de la Abuela's, Net Weight: 22.5oz. (638g), 5 units per package, Vacuum seal packages and twist tie bags, KEEP REFRIGERATED. UPC 850283002037
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1569-2025·2025-04-23

    Hip Implant Liner Mislabeled as Standard Instead of Hooded Design

    A total of 16 acetabular liners for the Cordera Hip System were mislabeled—packaged as hooded liners but labeled as standard models. The recall affects devices from Lot 1788258 distributed in CA, FL, NV, and TN.

    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-0718-2025·2025-04-16

    Victor Packing Dried Cranberries Recalled for Carbohydrate Content Misbranding

    Victor Packing Inc. is recalling Dried Cranberries because the product label incorrectly states 2g total carbohydrates instead of the actual 27g. The affected products were distributed across multiple states.

    Product
    Dried Cranberries (21.75 lb/case; 300 - 1.16 oz packages/case)
    Category
    Food
    Distribution
    9 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-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-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
  • 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