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.

376–400 of 1381

HighFDA (Food)·F-0039-2025·2024-10-23
Lemonland Food Corp Recalls Perilla Leaves in Soybean Paste for Undeclared Wheat and Sesame
Lemonland Food Corp recalls Item FLD1000A Perilla Leaves in Soybean Paste distributed in Washington. The product label omits wheat and sesame seeds, which are present in the product.
Product
Item FLD1000A, Perilla Leaves in Soybean Paste, distributed in plastic clamshell containers, net wt. 0.315lb. The H-Mart label declares Perilla Leaves, Soybean Paste.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0121-2025·2024-10-23
Open Heart Surgical Kit Recalled for Incorrect Vessel Cannulae Model Labeling
Medline Industries is recalling 123 kits of its Open Heart Pack after discovering that model 30001 vessel cannulae were incorrectly labeled as model 30000. This labeling error could lead to use of the wrong surgical instrument during open heart procedures.
Product
MEDLINE OPEN HEART PACK, REF DYNJ66216C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0013-2025·2024-10-23
First Aid Antiseptic Ointment Recalled for Mislabeled Inactive Ingredients
Rugby Laboratories is recalling First Aid Antiseptic (Povidone-Iodine 10%) ointment because the product contains undeclared inactive ingredients not listed on the label.
Product
FIRST AID ANTISEPTIC — FIRST AID ANTISEPTIC (POVIDONE-IODINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0086-2025·2024-10-23
Leica Biosystems Cryostat lacks warning for flammable freezing spray use
Leica Biosystems Cryostat Model CM1510 S is recalled due to missing warning labels about flammable freezing sprays, which can ignite and cause serious injury. The device labeling lacked fire hazard warnings prior to 2019.
Product
Leica Biosystems Cryostat Model Number CM1510 S, Material Numbers: a) 491510C002, b) 1491510C003; for freezing and sectioning tissue samples
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0050-2025·2024-10-23
Stir Fried Dried Shrimp Recalled for Undeclared Wheat Allergen
Lemonland Food Corp recalled stir-fried dried shrimp (Item FLD1971) distributed in Washington because wheat is not declared on the label, despite being present in the product.
Product
Item FLD1971, Stir Fried Dried Shrimp, distributed in plastic clamshell containers. Net wt. 0.165lb. The H-Mart label declares: Shrimp, Sesame Oil, Soy Sauce, Corn Syrup, Salt
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0122-2025·2024-10-23
Medline Open Heart Surgical Kit Recall for Model Labeling Error
Medline Industries recalls certain open-heart surgical kits (Lot 23LBR364) due to incorrect model labeling, where model 30001 units were labeled as model 30000. The recall affects 30 units distributed nationwide.
Product
MEDLINE OPEN HEART, REF DYNJ904261B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0119-2025·2024-10-23
Medline Heart CABG Cannulae Recalled Due to Incorrect Model Labeling
Medline Industries is recalling 15 kits of MEDLINE HEART CABG DLP Vessel Cannulae due to incorrect model labeling discovered during manufacturing.
Product
MEDLINE HEART CABG CDS, REF CDS983376R
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0051-2025·2024-10-23
El Gallo Azul Processed Cheese Recalled for Non-English Labeling
El Gallo Azul Cock Brand Queso Procesado processed cheese in 300g metal cans is recalled for non-English labeling. The product was distributed in Oregon.
Product
El Gallo Azul Cock Brand Queso Procesado/Processed Cheese 300g packaged in a metal can
Category
Food
Distribution
0 states
ModerateFDA (Devices)·Z-0123-2025·2024-10-23
Medical Device Kit Incorrectly Labeled With Wrong Model Number
Medline Industries recalls MEDLINE KIT CV I II vessel cannulae kits because product for model 30001 was incorrectly labeled as model 30000 during manufacturing.
Product
MEDLINE KIT CV I II, REF DYNJ906071B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0021-2025·2024-10-16
Trevo Trak 21 Microcatheter Distributed with Incorrect Instructions and Labels
Stryker Neurovascular is recalling Trevo Trak 21 Microcatheters because Out-of-US approved instructions and labels were distributed instead of US-approved versions. Affected customers in CA and VA should contact the manufacturer.
Product
The Trevo Trak 21 Microcatheter is a single-lumen, braided shaft, variable stiffness catheter with radiopaque marker(s) on the distal end and a luer hub on the proximal end. The catheter shaft has a hydrophilic coating on the distal 100cm to reduce friction during use. The radiop
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0025-2025·2024-10-16
Coca-Cola recalls Minute Maid Zero Sugar Lemonade due to mislabeling
COCA COLA Consolidated LLC recalls Minute Maid Zero Sugar Lemonade cartons sold in Indiana, Kentucky, and Ohio. Regular Minute Maid Lemonade cans were incorrectly placed in Zero Sugar packaging.
Product
Minute Maid Zero Sugar Lemonade 12 cans carton UPC 0 25000 12115 9 CANNED UNDER THE AUTHORITY OF THE COCA-COLA COMPANY, ATLANTA, GA
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0022-2025·2024-10-16
FastPack TSH Calibrator Kit Recalled Due to Incorrect Barcode
Qualigen Inc is recalling the FastPack TSH Calibrator Kit due to an incorrect barcode linked to incorrect information. The barcode defect may allow successful system calibration, but TSH test results obtained could be higher than expected.
Product
FastPack TSH Calibrator Kit, REF: 25000024, For use in conjunction with the FastPack IP TSH Immunoassay and FastPack IP System Analyzer
Category
Medical Device
Distribution
25 states
ModerateFDA (Devices)·Z-0040-2025·2024-10-16
Inspire Respiratory Sensing Lead Model 4340 Serial Number Label Mismatch
FDA recall of 152 Inspire Model 4340 Respiratory Sensing Lead units due to a labeling error—the serial number printed on the product box does not match the actual serial number of the device inside.
Product
Inspire Model 4340 Respiratory Sensing Lead, component of the Inspire Upper Airway Stimulation (UAS) system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0024-2025·2024-10-16
iCast Covered Stent Recalled for Unique Device Identifier Labeling Error
Atrium Medical Corporation is recalling 11 iCast Covered Stents (Model 42616) due to an error in the Unique Device Identifier (UDI) printed on the distribution label. No illnesses or injuries have been reported.
Product
iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0041-2025·2024-10-16
Inspire Model 4063 Stimulation Lead Labeling Error — Serial Number Mismatch
Inspire Medical Systems is recalling 457 Model 4063 Stimulation Leads because the serial number on the shelf box does not match the serial number of the device inside, creating identification and traceability issues.
Product
Inspire Model 4063 Stimulation Lead, component of the Inspire Upper Airway Stimulation (UAS) system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0016-2025·2024-10-09
Raisin Bran Muffins Recalled for Undeclared Milk and Wheat Allergens
The Posh Bakery, Inc. is recalling Whole Grains Bakery Raisin Bran Muffins (6 oz) due to undeclared whey (milk) and wheat allergens and missing allergen labeling.
Product
Whole Grains Bakery labeled "Raisin Bran Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC "7 13583 05 104 7"
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-3207-2024·2024-10-09
Percussionaire IPV In-Line Valve Recall: Blue Cap Removal Labeling Update
Percussionaire is recalling the P5-TEE IPV in-line valve to update labeling and ensure the blue cap is removed before use and delivery of the device.
Product
Percussionaire, Inc., REF: P5-TEE, Qty: 1, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0017-2025·2024-10-09
Chocolate chip muffins recalled for undeclared milk and wheat
The Posh Bakery is recalling Whole Grains chocolate chip muffins due to undeclared milk and wheat allergens with missing allergen labeling. Those with milk or wheat allergies should not consume this product.
Product
Whole Grains Bakery labeled "Choclate Chip Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 105 4"
Category
Food
Distribution
0 states
HighFDA (Food)·F-0018-2025·2024-10-09
Blueberry muffins recalled for undeclared milk and wheat allergens
The Posh Bakery, Inc. is recalling Whole Grains Blueberry Muffins (6 oz) due to undeclared milk (whey) and wheat flour, with missing allergen labeling and nutrition facts panel.
Product
Whole Grains Bakery labeled "Blueberry Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 102 3"
Category
Food
Distribution
0 states
HighFDA (Food)·F-0015-2025·2024-10-09
Apple Cinnamon Muffins recalled for undeclared milk and wheat
The Posh Bakery is recalling Apple Cinnamon Muffins due to undeclared milk (whey) and wheat flour. The product lacks a nutrition facts panel and allergen statement, posing a risk to consumers with allergies to these ingredients.
Product
Whole Grains Bakery labeled "Apple Cinnamon Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC "7 13583 05 109 2"
Category
Food
Distribution
0 states
HighFDA (Food)·F-0020-2025·2024-10-09
Banana nut muffins recalled for undeclared milk and wheat allergens
The Posh Bakery recalls Whole Grains Bakery Banana Nut Muffins (6 oz) due to undeclared milk and wheat allergens. The muffins lack required allergen-contains statements and nutritional fact labels.
Product
Whole Grains Bakery labeled "Banana Nut Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 101 6"
Category
Food
Distribution
0 states
HighFDA (Food)·F-1836-2024·2024-10-09
Mini Raspberry Lemon Coffee Cake Recalled for Undeclared Walnuts and Wheat
Mini Raspberry Lemon Coffee Cake products in Washington were mislabeled and contain undeclared walnuts and wheat. Consumers with allergies to these ingredients should not consume the product and should return it to the store.
Product
Mini Raspberry Lemon Coffee Cake, net wt. 13.5oz. UPC 8 57297 00745 4. Made with Gluten-Free Ingredients in a Gluten-Friendly Bakery. Macrina Bakery - Kent, WA. Ingredients: CANE SUGAR, GREEK YOGURT (GRADE A PASTEURIZED CULTURED MILK, CREAM, NONFAT MILK), EGGS, RASPBERRIES, B
Category
Food
Distribution
1 state
HighFDA (Food)·F-0019-2025·2024-10-09
Whole Grains Bakery Lemon Muffins Recalled for Undeclared Milk and Wheat
The Posh Bakery is recalling Whole Grains Bakery Lemon Muffins (6 oz) due to undeclared milk and wheat allergens. The product lacks a nutrition facts panel and contains statement.
Product
Whole Grains Bakery labeled "Lemon Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC" 7 13583 05 106 1"
Category
Food
Distribution
0 states
HighNHTSA·24V327000·2024-10-05
2024-2025 BMW X5 Tire Placard May Display Incorrect Size and Pressure
BMW is recalling certain 2024-2025 X5 xDrive40i models because the tire information placard may display incorrect tire size and pressure, potentially leading to improper tire installation or inflation and increased crash risk.
Product
BMW — 2024 BMW X5
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3191-2024·2024-10-02
Custom Procedure Kit Sheath Introducers Mislabeled by Size
Merit Medical Systems is recalling Custom Procedure Kits (REF: K12T-11077) with 7F sheath introducers that are incorrectly labeled as 7.5F, a labeling discrepancy affecting 24 units distributed nationwide.
Product
Custom Procedure Kit, REF: K12T-11077
Category
Medical Device
Distribution
Distributed nationwide