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.

26–50 of 1381

HighFDA (Food)·H-0673-2026·2026-04-29
Instant horchata drink recalled nationwide for undeclared milk allergen
EL MEXICANO horchata drink is recalled for undeclared milk allergen. The voluntary recall affects products in the U.S., Canada, and Japan.
Product
EL MEXICANO horchata casera Instant Horchata Drink NET WT 14oz (396g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95138 UPC: 042743190266 Item: 102284
Category
Food
Distribution
29 states
HighFDA (Devices)·Z-1939-2026·2026-04-29
Diversatek Healthcare Viper Balloon Dilator catheter inflation tag error
Diversatek Healthcare is recalling Viper 3-Stage Wire Guided Balloon Dilators because the catheter inflation tag may contain an incorrect part number with wrong balloon diameter sizes and inflation pressures.
Product
Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 12mm-13.5mm-15mm, REF 1205-15
Category
Medical Device
Distribution
19 states
HighFDA (Devices)·Z-1941-2026·2026-04-29
Diversatek Viper Wire Guided Balloon Dilator Inflation Tag Incorrect
Diversatek Healthcare is recalling Viper 3-Stage Wire Guided Balloon Dilators because the attached inflation tag may contain an incorrect part number with wrong balloon diameter sizes and inflation pressures.
Product
Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 18mm-19mm-20mm, REF 1205-20
Category
Medical Device
Distribution
19 states
HighFDA (Devices)·Z-1940-2026·2026-04-29
Diversatek Viper Balloon Dilator Recall Due to Incorrect Inflation Specifications
Diversatek Healthcare has recalled the Viper 3-Stage Wire Guided Balloon Dilator because the inflation tag may contain incorrect balloon diameter sizes and inflation pressures. The incorrect specifications could affect proper device use during medical procedures.
Product
Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 15mm-16.5mm-18mm, REF 1205-18
Category
Medical Device
Distribution
19 states
LowFDA (Drugs)·D-0490-2026·2026-04-29
Monsel's Solution ferric subsulfate vials recalled for incorrect expiration date printing
Premier Dental Products is recalling Monsel's Solution (ferric subsulfate) 8 mL vials because the expiration date on the vial itself is printed with an extra digit (2709114 instead of 270914). The carton expiration date is correct.
Product
MONSELS SOLUTION — MONSELS SOLUTION (FERRIC SUBSULFATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0681-2026·2026-04-22
Pure Palm Medjool Dates Recalled for Coconut Allergen Mislabeling
Pure Palm Medjool Dates (UPC 852160007005, LOT PP0576D1) are being recalled because the product contains coconut but the label does not disclose this allergen, posing a risk to consumers with coconut allergies.
Product
Label is predominantly green with white lettering in a clear plastic clamshell container. Pure Palm dates- Medjool Dates Net Wt. 16OZ UPC: 852160007005
Category
Food
Distribution
0 states
ModerateFDA (Drugs)·D-0481-2026·2026-04-22
FDA Recalls Skin Rehab Hydrocortisone Balm Nationwide for Subpotency
Island Kinetics is recalling Skin Rehab Calming Skin Gel nationwide due to subpotency. The product labeled as containing 1% hydrocortisone actually contains less active ingredient than stated.
Product
Skin Rehab, Calming Skin Gel, Hydrocortisone Balm, hydrocortisone 1%, .53oz net wt. (15.3g) per bottle, Distributed By: A.C.E. Inc., DFW Intl. Airport, Texas 75261, www.RHONDAALLISON.COM. NDC 66915-531-04
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0650-2026·2026-04-15
Zarlengo's Chocolate Chocolate Chip Gelato Recalled for Undeclared Soy Allergen
Zarlengo Italian Ice is recalling Chocolate Chocolate Chip Gelato in multiple sizes because soy lecithin is listed in the ingredients but soy is not declared in the allergen statement, posing a risk to consumers with soy allergies.
Product
Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon bucket/pail and 2-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminat
Category
Food
Distribution
3 states
HighFDA (Food)·H-0651-2026·2026-04-15
Zarlengo's Chocolate Gelato recalled for undeclared soy allergen
Zarlengo's Chocolate Gelato is recalled because soy lecithin is in the product but soy is not listed in the allergen contains statement. The mislabeling affects people with soy allergies.
Product
Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1780-2026·2026-04-15
Cook Medical Tracheostomy Introducer Tray Labeled with Excessive Expiration Dates
Cook Medical is recalling 441 units of its Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray, which were labeled with expiration dates exceeding the actual shelf life. The recalled devices were distributed worldwide.
Product
COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: Reference Part Number C-PTISY-100-HC-G-NA, Order Number G57703; Reference Part Number C-PTISY-100-UNL-HC-G-NA, Order Number G57706; Reference Part Number C-PTISY-100-UNS-HC-G-NA, Order Number G57704
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1792-2026·2026-04-15
COOK MEDICAL Wayne Pneumothorax Tray: Incorrect Expiration Date Labeling
Cook Medical issued a Class II recall of 318 Wayne Pneumothorax Trays distributed worldwide because the devices were labeled with expiration dates exceeding their true shelf life.
Product
COOK MEDICAL Wayne Pneumothorax Tray: Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537; Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537; Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537; Reference Par
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1769-2026·2026-04-15
Tornier HRS Max Shoulder Implant Parts Mislabeled With Wrong System Compatibility
Tornier HRS Max orthopedic implant parts were mislabeled as compatible with the HRS Max system, but are actually compatible only with the older HRS system and will not work with HRS Max components.
Product
Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max Tuberosity Body No Coat, Small, Cat. No. ARS1041102 3. TORNIER HRS Max Trial, Cat. No. ARS10252
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0637-2026·2026-04-08
Divided Sunset Multi Collagen Peptides Missing Allergen Labeling
TG FOODS INC is recalling Divided Sunset Multi Collagen Peptides (8 oz) because the product contains eggshell membrane collagen and wild-caught marine collagen but fails to declare EGG and the specific fish species on the label.
Product
Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Pouch, UPC Code: 8 50005 60689 5
Category
Food
Distribution
28 states
HighFDA (Food)·H-0649-2026·2026-04-01
Doraditas de Azucar recalled due to missing allergen labeling
Distribuidora de Alimentos Sendero LLC is recalling Doraditas de Azucar because the product label is missing declarations for wheat and soy allergens.
Product
Doraditas de Azucar UPC 5901234123457
Category
Food
Distribution
0 states
HighFDA (Food)·H-0631-2026·2026-04-01
Favorina Chocolate Ladybugs Recalled for Undeclared Tree Nut
Lidl US is recalling Favorina Chocolate Ladybugs German-Style Nougat because the label does not specify which tree nut is contained in the product, posing a risk to consumers with tree nut allergies.
Product
Favorina Chocolate Ladybugs German-Style Nougat, Net Wt 3.52 oz (100g). UPC 2030 4492. Distributed By Lidl US, LLC, 3500 S. Clark St, Arlington, VA 22202. Product of Germany.
Category
Food
Distribution
10 states
HighFDA (Food)·H-0623-2026·2026-04-01
Pan de Bono Cheese Bread Recalled for Undeclared Soy Allergen
South Florida Food, LLC is recalling Pan de Bono (Cheese Bread) because the product contains undeclared soy, a common allergen that poses a health risk to consumers with soy allergies.
Product
Pan de Bono (Cheese Bread), 100 units per Paper Cardboard Box, Net Wt 14.4 lb. KEEP FROZEN
Category
Food
Distribution
1 state
HighFDA (Food)·H-0602-2026·2026-04-01
Bulk Colustrum Powder Missing Milk Allergen Declaration
Herbal Creations USA is recalling bulk packaged Colustrum Powder because the product label does not declare milk as an allergen ingredient, posing a risk to consumers with milk allergies.
Product
Bulk packaged Colustrum Powder. packaged with generic product label.
Category
Food
Distribution
0 states
ModerateFDA (Devices)·Z-1651-2026·2026-04-01
Embrace Drill Tower Shoulder Instruments Recalled for Incorrect Article Numbers
Waldemar Link is recalling 75 units of the Embrace Shoulder Drill Tower because the surgical technique overview contains incorrect article numbers. The individual surgical steps remain correct despite the documentation error.
Product
Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;
Category
Medical Device
Distribution
15 states
LowFDA (Devices)·Z-1618-2026·2026-04-01
Philips 3D6-2 Ultrasound Transducers Recalled for Labeling Clarification
Philips Ultrasound recalls 17 units of the Philips 3D6-2 Ultrasound Transducer to provide clarification and labeling that defines the device's useful life.
Product
Philips 3D6-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·N/A·2026-03-25
White Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
Shaman Botanicals, LLC is recalling White Vein Advanced Alkaloids Chewable Tablets because testing found the active ingredient 7-hydroxymitragynine is present in a quantity greater than the labeled specification.
Product
Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 3
Category
Food
Distribution
0 states
ModerateFDA (Devices)·Z-1574-2026·2026-03-25
Artegraft Vascular Graft recalled for incorrect lot labeling on outer packaging
LeMaitre Vascular is recalling Artegraft Vascular Graft (REF# AG740) due to a labeling mix-up where outer packaging has incorrect lot information. No illnesses or injuries have been reported.
Product
Artegraft Vascular Graft; REF#: AG740;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1548-2026·2026-03-18
Blood glucose monitor instructions recalled for unclear error code labeling
Trividia Health is recalling TRUE METRIX GO blood glucose monitor instruction manuals because the labeling fails to clearly explain what an E-5 error code means or when to seek medical help, risking delayed treatment for high blood glucose emergencies.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX GO Kit/RF4001-01BK, CVS TRUE METRIX GO Kit/RF4007-01, Meijer TRUE METRIX GO Kit/RF4019-01, Fred's Phamarcy TRUE METRIX GO Kit/R
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1546-2026·2026-03-18
Blood Glucose Meter Instructions Inadequately Label Critical E-5 Error Code
Trividia Health recalls Owner's Booklets for TRUE METRIX PRO blood glucose meters because labeling inadequately explains the E-5 error code, which can represent very high blood glucose levels. Unclear instructions could delay medical attention when users experience this critical error.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Description/Item: TRUE METRIX PRO Meter Only/RE4H01P-40, TRUE METRIX PRO Starter Kit/RE4H01P-43, PROCURE TRUE METRIX PRO Meter Only/RE4212P-00, Henry Schein TRUE MET
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1496-2026·2026-03-18
Syringe Recall: Luer Slip Syringes Incorrectly Packaged in Luer-Lok Batches
BD is recalling 204,000 units of 10mL non-sterile Luer-Lok syringes because Luer Slip syringes were mistakenly packaged in batches marked for Luer-Lok. The recall affects units distributed in California and Texas.
Product
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0554-2026·2026-03-18
Coco's Italian Market Cannoli Making Kit Missing Allergen Declarations
Coco's Italian Market Cannoli Making Kit is recalled because the label lists flour and ricotta cheese as sub-ingredients but fails to declare wheat and milk allergens. Consumers with wheat or milk allergies may be at risk if they consume the product.
Product
Coco's Italian Market Cannoli Making Kit with 6 Cannoli Shells & Cream, Net Wt. 8 oz. (227g), Keep Frozen, packaged in a plastic container, UPC 0680334992716
Category
Food
Distribution
1 state