Hazard

Mislabeling recalls

256 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 mislabeling 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.

26–50 of 256

HighFDA (Food)·H-0648-2025·2025-09-24
Charge-Up Chilaquiles Recalled for Undeclared Yellow Food Dyes
Itacate Foods LLC is recalling 566 packages of Charge-Up Chilaquiles due to undeclared Yellow #5 and Yellow #6 dyes. Consumers with sensitivities to these food additives should not consume the product.
Product
CHARGE-UP CHILAQUILES Traditional Mexican breakfast consisting of tortilla chips smothered in a spicy tomatillo salsa and beans, topped with egg and cheese. NET WT 3.5 OZ (100G) INGREDIENTS: *** VEGETABLE FLAVOR BASE (SALT, SUGAR, SOYBEAN OIL, ONION POWDER, CORN STARCH, MALTODEXT
Category
Food
Distribution
26 states
LowFDA (Food)·H-0594-2025·2025-09-24
Dietary Supplement Quercetin Recalled for Unapproved Drug Claims
Hi-Tech Pharmaceuticals is recalling Quercetin dietary supplements (Lot C1612) due to unapproved drug claims and misbranding.
Product
HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM SUPPORTS RESPIRATORY HEALTH SUPPORTS CARDIOVASCULAR HEALTH 120 TABLETS DIETARY SUPPLEMENT UPC 8 11836 02491 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
Category
Drug
Distribution
50 states
ModerateFDA (Drugs)·D-0642-2025·2025-09-17
Amphetamine prescription tablets recalled for strength mislabeling error
Lannett Company recalls amphetamine tablets for strength labeling errors. Two bottles in Ohio were found to contain 5mg tablets instead of the labeled 10mg.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
1 state
HighFDA (Food)·H-0567-2025·2025-09-10
Pecan Toffee Clusters Recalled Due to Undeclared Tree Nut Allergen
The Candy Barn recalls Pecan Toffee Clusters (5oz packages) because pecan allergen was not declared on the label. Consumers with tree nut allergies face risk of allergic reaction.
Product
Pecan Toffee Clusters, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 5oz, flexible plastic bag
Category
Food
Distribution
1 state
HighFDA (Food)·H-0558-2025·2025-09-10
Hans Kissle Red Bliss Potato Salad Recalled for Undeclared Wheat
Hans Kissle Red Bliss Potato Salad is being recalled because units labeled as potato salad actually contain pasta salad with undeclared wheat, posing a health risk to individuals with wheat allergies.
Product
Hans Kissle Red Bliss Potato Salad
Category
Food
Distribution
5 states
HighFDA (Drugs)·D-0597-2025·2025-09-03
Enoxaparin Sodium injection recalled for mislabeled dosage concentration
Bags of Enoxaparin Sodium Injection labeled as 80 mg/0.8 mL contained the 30 mg/0.3 mL concentration. This mislabeling could lead to incorrect dosing if providers or patients rely on the outer bag label.
Product
ENOXAPARIN SODIUM — ENOXAPARIN SODIUM (ENOXAPARIN SODIUM)
Category
Drug
Distribution
1 state
HighFDA (Devices)·Z-2479-2025·2025-09-03
Medline Surgical Kits Recalled for Incorrect Foley Tray Information
Medline surgical kits containing BD SureStep Foley Tray Systems have been recalled due to incorrect product information insert sheets that could lead to patient injury, including infection or allergic reaction.
Product
Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTIC DYNJG001004A LAVH MINOR DYNJG901001B CRANIOTOMY DYNJ908819B KIT CRANIOTOMY (only units from SKU DYNJG001004A LAVH MINOR were distributed)
Category
Medical Device
Distribution
2 states
HighFDA (Food)·H-0454-2025·2025-08-20
Soda Biscuits Recalled for Undeclared Milk and Wheat Allergens
Shang Hao Jia, Inc. is recalling soda biscuits that do not declare all allergen ingredients (milk powder and wheat). People with milk or wheat allergies could be affected.
Product
Soda Biscuit (Sea Salt Fresh Milk Flavor), Net Wt: 360g/12.07oz; Shelf life: 10 months; Manufacturer: Zhejiang Dinggian Industrial Co., Ltd. Importer: Shang Hao Jia., Inc. UPC: 6 970425 865031
Category
Food
Distribution
0 states
ModerateFDA (Food)·H-0445-2025·2025-08-20
Lithium Orotate Supplement Recalled Due to Below-Labeled Potency
Enjoy Nutrition, LLC is recalling Lithium Orotate 10MG supplements that fail to meet labeled potency due to a supplier ingredient issue. Approximately 159,926 units were distributed nationwide through Amazon and other retailers.
Product
Lithium Orotate, 10MG, Distributed by Enjoy Nutrition, LLC. UPC#: 702730894033, 702730894057
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0381-2025·2025-08-06
Sweetener bottles mislabeled as Pure Monk Fruit contain Stevia powder
NuNaturals Inc is recalling 78 bottles of Pure Monk Fruit Sweetener nationwide due to mislabeling; the bottles actually contain Stevia powder. Consumers should stop using this product.
Product
Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187 6. Product is packaged in a plastic bottle with white cap. Ingredient: Monk Fruit (Luo Han Guo) Extract. Monk Fruit is so much sweeter than sugar, a pinch is all you need. Suggested Use: Add to sweeten your food or be
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0542-2025·2025-08-06
Amlodipine Besylate and Benazepril Capsules Recalled for Incorrect Expiration Date Label
Lupin Pharmaceuticals is recalling 7,668 bottles of Amlodipine Besylate and Benazepril Hydrochloride capsules distributed nationwide due to incorrect expiration dates on the label.
Product
AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE — AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE (AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2074-2025·2025-07-09
BD Heyman Follower Straight Tip Catheters Recalled for Incorrect Size Labeling
C.R. Bard Inc is recalling BD Heyman Follower Straight Tip catheters due to packaging that may contain incorrect French size information. The recall affects units distributed nationwide in the US and Canada.
Product
BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0079-2025·2025-07-02
Nature Mills Horsegram Soup Recalled for Undeclared Wheat Allergen
NatureMills US Incorporated is recalling Nature Mills Horsegram Soup due to undeclared wheat allergens. The product may contain wheat not declared on the label, posing a risk to consumers with wheat allergies.
Product
Nature Mills Horsegram Soup, 100g
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-2009-2025·2025-07-02
Shoulder Replacement Screws Recalled for Package Size Mislabeling
Encore Medical is recalling Altivate Reverse Torx Peripheral Screws used in shoulder replacement surgery because the package labeling indicates a different size than the product it contains.
Product
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 22mm Model/Catalog Number: 506-04-122 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-1976-2025·2025-06-25
Hearing Aid Labeling Error and UDI Non-Compliance Recall
AcoSound hearing aid models are being recalled due to labeling errors and incomplete UDI (Unique Device Identification) information. Affected units have incorrect manufacturer information and missing required compliance documentation.
Product
AcoSound. Model Number: LW12-BTE-M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0017-2025·2025-06-18
Rocky Road Ice Cream Recall: Undeclared Almonds and Conflicting Labels
Rocky Road Ice Cream (1.5 qt) is being recalled due to conflicting allergen labeling. The tub states 'may contain tree nuts' but the lid declares almonds as an ingredient, creating a hazard for consumers with tree nut allergies.
Product
Rocky Road Ice Cream packaged in a Breyer Chocolate Truffle Tub that says "may contain tree nuts" with a Breyers Rocky Road Ice Cream Lid that declares almonds as an ingredient. 1.5 qt
Category
Food
Distribution
0 states
HighFDA (Food)·F-0937-2025·2025-06-18
Vern's Foods frozen geoduck chowder recalled for undeclared fish allergen
Vern's Foods & Farm is recalling Taylor Shellfish Farms Geoduck Chowder Base because the product contains fish (anchovies) not declared on the label. Consumers with fish allergies should not consume this product.
Product
Taylor Shellfish Farms Geoduck Chowder Base, frozen, Ingredients: Potatoes, Clam (Geoduck) ***Butter (Cream, Salt), Fish Sauce Ka Me***CONTAINS: MILK, CLAMS. Product is packed in rigid plastic tubs. Net wt. 16 oz. Produced with local, farm fresh ingredients by: Vern's Foods &
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-0936-2025·2025-06-18
NOW Nutritional Yeast Powder Recall: Regular Yeast Packaged Incorrectly
NOW Foods is recalling 18,658 units of NOW Nutritional Yeast Powder because regular yeast was inadvertently packaged in the product. Affected lot numbers are 3372888 and 3320523.
Product
NOW Nutritional Yeast Powder, Nt. Wt. 10oz. UPC 7 33739 02460 2
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0825-2025·2025-06-11
Gluten-free sourdough bread recalled for undeclared egg allergen
NEW GRAINS GLUTEN FREE BAKERY is recalling approximately 42 units of its Artisan Sourdough Bread (32 oz) distributed in Utah due to printing defects that render the egg allergen declaration illegible.
Product
Artisan Sourdough Bread: Gluten-free sourdough bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Eggs, Tapioca flour, Sugar, Potato flour, Palm fruit oil, Yeast, Psyllium husk powder, Vinegar, Sea salt, Xanthan gum, Powdered sugar.
Category
Food
Distribution
0 states
HighFDA (Drugs)·D-0458-2025·2025-06-11
Hand Sanitizer Recalled for Subpotent Ethyl Alcohol Content
Spectrum Advanced Gel Hand Sanitizer is recalled because it contains less ethyl alcohol than the labeled 70%. The product also displays a cloudy appearance, indicating a potential quality issue.
Product
HAND SANITIZER — HAND SANITIZER (ETHYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1817-2025·2025-06-04
Surgical stem implant mislabeled with 15mm diameter instead of 13mm
Onkos Surgical is recalling 23 ELEOS Collar Stem implants (model HC-13120-03M) mislabeled with 15mm diameter instead of 13mm. The affected implants were distributed in California, Kentucky, and Wisconsin.
Product
ELEOS COLLAR STEM, CEMENTED, FLUTED, 13MM X 120MM. Model Number: HC-13120-03M. Component of Limb Salvage System with BioGrip.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0813-2025·2025-06-04
Hummingbird Organic Roasted Salted Cashews Recalled for Undeclared Hazelnut
Hummingbird Organic Roasted Salted Cashews in 6-oz packages have been recalled for containing undeclared hazelnut. The product was distributed in California, Oregon, and Washington.
Product
Kraft package is labeled as Hummingbird Organic Roasted Salted Cashews, net wt. 6oz.
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1818-2025·2025-06-04
ELEOS Collar Stem Implants Recalled for Size Mislabeling in Package
Onkos Surgical recalls 23 ELEOS Collar Stem implants with incorrect sizing labels. Packages marked for 13mm implants contained 15mm diameter implants, risking surgical complications.
Product
ELEOS COLLAR STEM, CEMENTED, FLUTED, 15MM X 120MM. Model Number: HC-15120-03M. Component of Limb Salvage System with BioGrip.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0804-2025·2025-05-21
Blueberry Lemon Scones Recalled for Undeclared Soy Allergen
Blueberry Lemon Scones sold at a Tennessee retailer are recalled for an undeclared soy allergen. Consumers with soy allergies should not consume this product.
Product
Blueberry Lemon Scones, bulk packaged in bakery boxes. Products are sold at retail in pastry cases and not individually labeled.
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-1745-2025·2025-05-21
Meddev Contour Gold Eyelid Weight recalled for mislabeling
Meddev Corp is recalling 34 Contour Gold Eyelid Weight implants (Model LL3012, Lot 7228) due to mislabeling. The recall affects units distributed nationwide across 17 states.
Product
Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3012 Product Description: Contour Gold Eyelid Weight, 1.2 gm MedDev Contour and ThinProfile Eyelid Weight Implants are designed for the gravity-assisted treatment of protracted permanent
Category
Medical Device
Distribution
Distributed nationwide