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.

51–75 of 256

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
ModerateFDA (Devices)·Z-1723-2025·2025-05-14
Ambu aScope 5 Broncho HD Bronchoscope Sampler Set Labeling Error
Ambu aScope 5 Broncho HD Sampler Set units have incorrect front label specifications. The front label lists 5.0/2.2 while the device is actually 5.6/2.8 as correctly labeled on the back.
Product
Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0732-2025·2025-04-30
MO-CHA Premium Non-Dairy Creamer Recalled for Undeclared Milk Allergen
MO-CHA brand Premium Non-Dairy Creamer is being recalled because the label does not declare milk, a major allergen. The product contains whey powder and casein but is missing allergen labeling required for consumer safety.
Product
MO-CHA brand Premium Non-Dairy Creamer; INGREDIENTS Glucose syrup, Refined vegetable oil, Whey powder, Sugar, Casein, Emulsifier (471, 481i), Stabilizer(340ii, 452i), Anti-caking agent(551), Food flavor; Shelf Life: 24 months; Net Weight (NET WT): 2.2 lbs (1kg); IMPORTED BY Momo
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1651-2025·2025-04-30
Stryker Latitude EV Humeral Stem Trial recalled for incorrect marking
A Stryker Latitude EV Humeral Stem Trial is recalled because the laser marking specifies incorrect specifications—150mm Large / Right instead of the actual 150mm Medium / Left, which could lead to wrong prosthesis implantation.
Product
stryker Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side: RIGHT, REF 9030103; Prosthesis, Elbow, Semi-Constrained, Cemented
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0716-2025·2025-04-23
Golden Crop Candy Recalled for Undeclared Food Coloring
Blooming Import Inc. is recalling Golden Crop Candy due to undeclared and unallowed food colors including Blue 1, Red 40, and Acid Red 18. The recalled candy was distributed across eight states.
Product
Golden Crop Candy (10 oz. (283g) wrapped candies)
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1509-2025·2025-04-09
BD Connecta Stopcocks Recalled for Non-U.S. Instructions Shipped to U.S. Market
BD Connecta Luer-Lok 360 stopcocks were distributed with non-U.S. instructions for use. Healthcare facilities should verify they have the correct U.S. instructions before using affected lot numbers.
Product
BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and hemodynamic pressure monitoring.
Category
Medical Device
Distribution
35 states
HighFDA (Food)·F-0667-2025·2025-04-02
Favorite Day Gourmet Cheesecake Recalled for Undeclared Pecan
Favorite Day Gourmet New York-Style Cheesecake is recalled for containing undeclared pecan, a tree nut allergen not listed on the product label. The product was distributed to California, Florida, Iowa, Ohio, and Texas.
Product
favorite day gourmet New York-Style CHEESECAKE 2 SLICES NET WT 6OZ (170 g) UPC 0 85239 09690 1 Target Brands, Inc.
Category
Food
Distribution
5 states
ModerateFDA (Devices)·Z-1432-2025·2025-04-02
Orthofix Pillar SA Ti Spacer System Mislabeled for Anterior Height
Orthofix is recalling Pillar SA Ti Spacer System spinal implants because the product label lists an incorrect anterior height of 10mm, while the actual device measures 10.5mm. This labeling discrepancy could affect surgical planning during implantation.
Product
Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device, sterile, implant grade titanium alloy: (1) REF 82-3300SP, 33mm W x 24mm D x 10mm H, 7 degrees; (2) REF 82-3700SP, 37mm W x 28mm D x 10mm H, 7 degrees; and (3) REF 82-4000SP, 40mm W x 32mm D x 10mm
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0302-2025·2025-04-02
Topical Hydrogen Peroxide Solution Recalled for Incorrect Back Label
Consumer Product Partners is recalling Hydrogen Peroxide Topical Solution bottles with incorrect back labels indicating 91% Isopropyl Alcohol. The labeling mixup affects 25,932 bottles distributed in Virginia.
Product
HYDROGEN PEROXIDE — HYDROGEN PEROXIDE (HYDROGEN PEROXIDE)
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-1434-2025·2025-04-02
Prelude IDEAL 4F Hydrophilic Sheath Introducer contains incorrect 5F dilators
Merit Medical Systems is recalling Prelude IDEAL 4F Hydrophilic Sheath Introducer units (Lot H3082668) that contain 5F dilators instead of the labeled 4F dilators, which may result in procedure delay.
Product
Prelude IDEAL 4 F Hydrophilic Sheath Introducer, REF: PID4F16021PW/D
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1271-2025·2025-03-12
Dental implant abutments recalled for incorrect packaging labels
Hiossen has recalled ET Rigid Abutment dental implant components because stickers in the packaging mislabel whether products are Mini or Regular versions. Incorrect identification could affect proper implant installation.
Product
ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. GA4515MP Model/Catalog Number: ETRGA4515MP
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1275-2025·2025-03-12
ET Rigid and Multi Dental Abutments Recalled for Incorrect Identification Stickers
Hiossen recalled ET Rigid and Multi dental abutments for incorrect identification stickers in packaging that misidentify product versions, risking improper placement during installation.
Product
ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4524MP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0533-2025·2025-02-12
Seasoned Bread Crumbs Recalled Due to Undeclared Sesame Allergen
La Fiesta Food Products is recalling seasoned bread crumbs because they contain undeclared sesame, an allergen not listed on the label. The product was distributed nationwide.
Product
La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned, NET WT 8 OZ. (227g), UPC# 032327000887
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1075-2025·2025-02-12
Levofloxacin Antimicrobial Susceptibility Discs Recalled Due to Packaging Mislabeling
Oxoid Limited is recalling 1,406 units of Lev5 Levofloxacin susceptibility discs because packaging may contain Norfloxacin discs instead, which could affect laboratory test results.
Product
Lev5, REF CT1587B, 50 Susceptibility discs Levofloxacin 5 ug, IVD, CE 2797
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-0982-2025·2025-01-29
Stryker 3.0MM Neuro Precision Head Recalled for Package Labeling Mismatch
Stryker is recalling the 3.0MM Precision Neuro Match Head due to a packaging discrepancy where the device may not match the product label. Approximately 1,489 units distributed worldwide are affected, including lot numbers 22179047, 22179027, and 22160017.
Product
stryker 3.0MM Precision Neuro Match Head, REF 5820-107-530, used to cut bone and bone cement during neurosurgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0419-2025·2025-01-29
Butter Toffee Almonds recalled for undeclared milk allergen
Cal Yee Farm LLC recalls Butter Toffee Almonds for undeclared milk. Products affected: Cal Yee's (8-oz, 1-lb bags) and Boa Vista (6-oz bag). Distribution: 2 California retail stores and online/phone orders to California and Pennsylvania.
Product
Cal Yee's Butter Toffee Almonds (8-oz, 1-lb plastic bags) Boa Vista Butter Toffee Almonds (6-oz plastic bag)
Category
Food
Distribution
2 states
HighFDA (Drugs)·D-0104-2025·2024-12-11
Sunitinib Malate Capsules Recalled Due to Label Mix-Up
AvKARE is recalling Sunitinib Malate 25 mg capsules nationwide due to a label mix-up in lot 100049501. The FDA has classified this as a Class II recall.
Product
SUNITINIB MALATE — SUNITINIB MALATE (SUNITINIB MALATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0346-2025·2024-11-20
Cook Approach CTO Micro Wire Guide recalled for incorrect expiration date labels
Cook Incorporated is recalling Approach CTO Micro Wire Guide devices due to incorrect expiration dates on affected lot labels. The recall affects 2,005 units in the US and 1,145 units overseas.
Product
Approach CTO Micro Wire Guide, Guide Wire, Catalog Prefix CMW; Reference Part Numbers: CMW-14-190-12G CMW-14-190-18G CMW-14-190-25G CMW-14-190-6G CMW-14-300-12G CMW-14-300-18G CMW-14-300-25G CMW-14-300-6G
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0037-2025·2024-10-23
Nuts.com recalls S'mores Bites for undeclared milk allergen
Nuts.com is recalling S'mores Bites due to undeclared milk allergen. Milk chocolate was listed in the product description but omitted from the ingredient list, creating a labeling mismatch.
Product
S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranford, NJ, 07016
Category
Food
Distribution
36 states
HighFDA (Food)·F-0028-2025·2024-10-23
Premium Pistachio Grapenut Ice Cream Recalled for Undeclared Yellow 5 and Yellow 6 Dyes
Today's Frozen Desserts, Inc. is recalling Premium Pistachio Grapenut ice cream sold in Florida because it contains undeclared Yellow 5 and Yellow 6 dyes. People sensitive to these food colorings should not consume the product.
Product
Premium Pistachio Grapenut, packaged in paper and plastic containers in sizes 3 Gallons, half gallons, and quarts. Keep Frozen
Category
Food
Distribution
0 states
HighFDA (Food)·F-0034-2025·2024-10-23
Bevi Flavor#115 Electrolytes Recalled: Mislabeled, Contains Caffeine
Hydration Labs Inc. is recalling Flavor#115 Electrolytes (3.78L BIB units) distributed nationwide and in Canada because the product is labeled as electrolytes but actually contains caffeine.
Product
Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN barcode 00850010449043. Product is packaged as a Bag In Box (BIB) single unit for use in Bevi Smart Water Cooler machines dispensing flavored waters.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0120-2025·2024-10-23
Medline Heart Overhead Table Pack recalled for incorrect model labeling
Medline Industries recalls Heart Overhead Table Packs due to incorrect labeling. Some kits were marked as model 30000 when they should be model 30001.
Product
MEDLINE HEART OVERHEAD TABLE PACK, REF DYNJ0778508J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3190-2024·2024-10-02
Prelude Sheath Introducer 7.5F devices recalled due to labeling error
Merit Medical Systems is recalling 1,892 Prelude Sheath Introducer devices due to a labeling error: devices labeled as 7.5F are actually sized as 7F. The dimensional mislabeling could result in incorrect device selection during medical procedures.
Product
Prelude Sheath Introducer 7.5F, REF: PSI-7F-11-038 Version F (PSI-7F-11-038/F)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3171-2024·2024-09-25
K-Wire Packaging Error Recall by Smith & Nephew
Smith & Nephew issued a voluntary recall of K-Wire bone fixation fasteners due to a packaging error where packages contained the wrong wire diameter than labeled.
Product
DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-3133-2024·2024-09-18
Biolox Taper Sleeve Mislabeling: Wrong Component Size in Hip Replacement
Zimmer GmbH is recalling Biolox Option Taper Sleeves due to mislabeling where packaging labels one neck size but contains the opposite size. These components are used in hip replacement surgery.
Product
Biolox Option Taper Sleeve, Type 1 Taper, -6mm Neck - Indicated for use in total hip replacement with cemented or non-cemented femoral and acetabular components. Item Number: 650-1064
Category
Medical Device
Distribution
Distributed nationwide