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.

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.

826–850 of 9606

HighFDA (Food)·F-0767-2023·2023-05-03
Baklava from Paximadi Co recalled for undeclared soybean oil
Paximadi Co LLC is recalling Baklava manufactured on 3/29/2023 for undeclared soybean oil. Consumers with soybean allergies should not consume the product.
Product
Baklava, 2 oz. Each cardboard box contains 25 units (net wt. 50 oz). No UPC. The Ingredients statement declares: Fillo (Enriched, Non-Bromine Bleached Wheat Flour, Thiamin, Mononitrate, Riboflavin, Niacin, Iron, Folic Acid, Water, Corn Starch, Vegetable Oil (Corn or Canola)***Wal
Category
Food
Distribution
1 state
HighFDA (Food)·F-0752-2023·2023-05-03
Enriched Hot Dog Buns Recalled for Undeclared Sesame Allergen
Our Family White Hot Dog Enriched Buns are being recalled due to undeclared sesame. The recall affects approximately 28,700 units distributed in Michigan, Ohio, Indiana, and Illinois, and poses a risk to consumers with sesame allergies.
Product
Our Family White Hot Dog Enriched Buns, 8 count 12oz. retail unit UPC 0-70253-75107-3
Category
Food
Distribution
4 states
ModerateFDA (Devices)·Z-1430-2023·2023-05-03
Caspar Cervical Retractor Basket Lids Recalled for Incorrect GTIN Labeling
Aesculap Implant Systems recalls Caspar Cervical Retractor (CCR) Basket lids with incorrect GTIN labeling. The product bears GTIN #04046955299592 instead of the correct #04046955299607.
Product
Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and ME764 Casper Cervical Retractor (CCR) Basket Full System - Lid Only. A lid to a container intended to provide a suitable platform for placing/containing many medical/surgical/dental instruments. Note: The CCR basket
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0736-2023·2023-04-26
Kagome Worchester Sauce Recalled for Undeclared Soy Allergen
Kagome Worchester Sauce in 16.9 fl. oz plastic bottles is recalled because it contains soy that is not declared on the label, posing a risk to consumers with soy allergies.
Product
Kagome Worchester Sauce 16.9 fl., oz plastic bottles
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0738-2023·2023-04-26
Sheila G's Gluten Free Reese's Pieces Brownie Brittle recalled for undeclared wheat
Sheila G's Gluten Free Reese's Pieces Brownie Brittle (4 oz bags, UPC 711747 011562) is being recalled because the product may contain undeclared wheat despite its gluten-free label, creating a risk for consumers with celiac disease or wheat allergies.
Product
Sheila G's Gluten Free Reese's Pieces Brownie Brittle, 4 oz bag (Retail bag UPC 711747 011562)
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0733-2023·2023-04-26
Dietary Supplement with Unapproved COVID-19 Treatment Claims Recalled
Natural Solutions Foundation is recalling a colloidal silver dietary supplement labeled to treat COVID-19. The product violates FDA regulations prohibiting disease claims on dietary supplements.
Product
Dr. Rima Recommends The Silver Solution Immune System Support Dietary Supplement Nano Silver 10 ppm 16 fl. oz. (473 ml)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0747-2023·2023-04-26
Natural Pak Coffee Chili Rub Contains Undeclared Bacon Glaze Ingredients
Natural Pak brand Coffee Chili Rub packages contain undeclared Bacon Glaze ingredients including demerara sugar, honey granules, maple sugar, cinnamon, allspice, clove, and parsley. The affected product was distributed in Ohio.
Product
Natural Pak brand Coffee Chili Rub is packaged in 22oz (624g), white, cylindrical, plastic containers; Ingredients: Sea salt, ancho chile, brown sugar, espresso beans, hot smoked paprika, mustard, black pepper, coriander, ginger, oregano, chipotle chile, paprika. Contains: mustar
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-1391-2023·2023-04-26
KLS E-Coupling Adapter Recalled for Incorrect Product Identifier Code
Pro-Dex Inc is recalling 199 KLS E-Coupling Adapter devices due to incorrect Unique Device Identifier (UDI) and GTIN codes. The devices were distributed nationwide.
Product
KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1398-2023·2023-04-26
Pressure Therapy System Recalled for Unauthorized Deep Vein Thrombosis Prevention Claim
Compass Health Brands is recalling the REX Pressure Therapy System because the user manual incorrectly claims the device can prevent deep vein thrombosis, an indication for which the device was not FDA-cleared.
Product
REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual. Intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas. Models: DVTREX-U and DVTREX -L
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1406-2023·2023-04-26
Avanos Ballard Oral Care Swabs recalled for incorrect expiration date labeling
Avanos Medical is recalling Ballard Oral Care Swabs (codes 12241, 12243, 12251) due to incorrect expiration date labeling. The recall affects 5,475 cases distributed worldwide.
Product
Avanos Ballard Oral Care Swab, Bulk Packed, Product Codes: a) 12241, b) 12243, c) 12251
Category
Medical Device
Distribution
Distributed nationwide
CriticalUSDA FSIS·015-2023·2023-04-21
Alef Sausage Recalls Halal Meat and Poultry Sausage Due to Misbranding
Alef Sausage Inc. is recalling ready-to-eat halal meat and poultry sausage products because they lacked required refrigeration labels, posing a risk of temperature abuse.
Product
Alef Sausage — Alef Sausage Inc. Recalls Ready-To-Eat Meat and Poultry Sausage Products Due to Misbranding and Possible Temperature Abuse
Category
Food
Distribution
3 states
SevereUSDA FSIS·014-2023·2023-04-21
Abbyland Foods Recalls Frozen Turkey Sausage Patties Due to Undeclared Soy
Abbyland Foods is recalling approximately 11,800 pounds of frozen turkey meatballs mislabeled as sausage patties because they contain undeclared soy.
Product
Abbyland Foods, Inc. — Abbyland Foods Recalls Frozen Turkey Sausage Patties Products Due to Misbranding and Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
HighUSDA FSIS·013-2023·2023-04-20
Bruno Beef Strips Recalls Pepper and Garlic Snack Sticks for Undeclared Soy
Bruno Beef Strips is recalling approximately 7,452 pounds of Pepper & Garlic snack sticks because the product contains undeclared hydrolyzed soy protein, a known allergen.
Product
Bruno Beef Strips Recalls Beef Strip Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
3 states
LowFDA (Drugs)·D-0535-2023·2023-04-19
Prescription Epinephrine Kits Recalled for Incorrect NDC Number on Carton
Focus Health Group is recalling 246 kits of Epinephrine Professional nationwide due to an incorrect NDC number printed on the outer carton. The labeling error does not affect the drug's safety or effectiveness.
Product
EPINEPHRINE PROFESSIONAL — EPINEPHRINE PROFESSIONAL (EPINEPHRINE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0692-2023·2023-04-12
Sysco Imperial Caesar Dressing Recalled for Egg Allergen Labeling Discrepancy
Sysco Imperial Caesar Dressing recalled due to labeling discrepancy. The outer case label indicates the product contains eggs, but the primary product label does not list eggs as an ingredient.
Product
Sysco Imperial Caesar Dressing NET CONTENTS 1 GAL (3.78 l) INGREDIENTS: Soybean Oil, Water, Distilled Vinegar, Parmesan Cheese***High Fructose Corn Syrup, Salt, Contains less than 2% of Ground Mustard, Spice, Dried Garlic, Anchovy Paste***Sodium Benzoate***Calcium Disodium EDTA**
Category
Food
Distribution
5 states
HighFDA (Food)·F-0695-2023·2023-04-12
Shirakiku Furikake Seasoned Seaweed Flakes Recalled for Incorrect Crustacean Labeling
Wismettac Asian Foods is recalling Shirakiku Furikake Seasoned Roasted Seaweed Flakes due to incorrect crustacean identification on the label. The product was distributed to 22 states.
Product
FURIKAKE SEASONED ROASTED SEAWEED FLAKES SEAFOOD Product number: 38245 Brand name: Shirakiku Distributed by: Wismettac Asian Foods, Inc. 13409 Orden Drive Santa Fe Springs, CA 90670
Category
Food
Distribution
22 states
LowFDA (Food)·F-0696-2023·2023-04-12
Shirakiku Furikake Seaweed Flakes Recalled for Incorrect Crustacean Labeling
Wismettac Asian Foods is recalling Shirakiku Furikake Seasoned Roasted Seaweed Flakes Spicy due to incorrect crustacean labeling. The company distributed 17,517 packages across 22 states.
Product
FURIKAKE SEASONED ROASTED SEAWEED FLAKES SPICY Product #38246 Brand name: Shirakiku Distributed by: Wismettac Asian Foods, Inc. 13409 Orden Drive Santa Fe Springs, CA 90670
Category
Food
Distribution
22 states
HighFDA (Food)·F-0683-2023·2023-04-05
Seasoned Seaweed Recalled for Undeclared Sesame and Wheat Allergens
Lemonland Food Corp is recalling Seasoned Seaweed distributed in Washington due to undeclared sesame seeds and wheat. Consumers with these allergies should not consume the product.
Product
Seasoned Seaweed distributed in un-labeled plastic containers 8oz and 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
Category
Food
Distribution
1 state
HighFDA (Food)·F-0682-2023·2023-04-05
Hot Pepper in Soy Sauce Recalled for Undeclared Soy and Wheat
Lemonland Food Corp recalled Hot Pepper in Soy Sauce distributed in 12-ounce containers due to undeclared soybean and wheat allergens. Consumers with soy or wheat allergies should not consume this product.
Product
Hot Pepper in Soy Sauce distributed in un-labeled plastic containers 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
Category
Food
Distribution
1 state
HighFDA (Food)·F-0652-2023·2023-04-05
Rold Gold Original Tiny Twists Pretzels Recalled for Undeclared Soy
Frito-Lay is recalling Rold Gold Original Classic Tiny Twists Pretzels because the product contains undeclared soy lecithin, which may affect consumers with soy allergies.
Product
Rold Gold Original Classic Tiny Twists Pretzels in 16oz UPC 2840004768 packaged in a flexible bag
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-1309-2023·2023-04-05
Leksell Stereotactic System Recall: Incorrect Instructions Distributed with Devices
Elekta Instrument AB is recalling 70 Leksell Stereotactic System neurosurgical devices due to incorrect Instructions for Use being distributed with the devices. Incorrect documentation for neurosurgical equipment could impact proper device use.
Product
Instructions for Use for the following Leksell Stereotactic System and Leksell Neurosurgical Instruments: (1) Part #A2800-26, Backlund Catheter Insertion Needle Kit III; (2) Part #A2800-15, Backlund Catheter Insertion Needle Kit I; (3) Part #A2600-01, Backlund Haematoma Evac
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0662-2023·2023-04-05
Seasoned Korean Lettuce Recalled for Undeclared Fish Allergen
Lemonland Food Corp recalled Seasoned Korean Lettuce distributed in Washington due to undeclared fish (anchovy). Consumers with fish allergies should not consume this product.
Product
Seasoned Korean Lettuce distributed in un-labeled plastic containers 6oz or 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1300-2023·2023-04-05
PCRopsis Reagent RVD-RT in vitro diagnostic kit recall for misleading labels
Entopsis, Inc. is recalling PCRopsis Reagent RVD-RT diagnostic kits due to misleading label statements that could affect proper use and test interpretation.
Product
PCRopsis Reagent RVD-RT, IVD: a) 1 mL, REF 78378001; b) 25 mL, REF 78378025; c) 100 mL, REF 78378100; Extraction-free PCR at room temperature; nucleic acid extraction from a variety of biological samples
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0657-2023·2023-04-05
Radish Kimchi recalled for undeclared fish and shellfish allergens
Lemonland Food Corp has recalled Radish Kimchi distributed in Washington due to undeclared fish (anchovy, sardinella) and shrimp. Consumers with allergies to fish or shellfish should not consume this product.
Product
Radish Kimchi distributed in un-labeled plastic containers 16oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
Category
Food
Distribution
1 state
HighFDA (Food)·F-0672-2023·2023-04-05
Seasoned Garlic Stem Recalled Due to Undeclared Fish and Sesame Allergens
Lemonland Food Corp recalled Seasoned Garlic Stem products due to undeclared fish (anchovy) and sesame allergens. Affected products were distributed in Washington from February 16-23, 2023.
Product
Seasoned Garlic Stem distributed in un-labeled plastic containers 8oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
Category
Food
Distribution
1 state