Hazard

Mis Labeling recalls

9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 9,622
Critical: 163
Severe: 590
Most recent: 2026-09-24

Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (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.

8926–8950 of 9622

HighFDA (Devices)·Z-0784-2013·2013-02-13
Lansinoh Thera Pearl Breast Therapy Hot and Cold Packs Recalled for Overheating Risk
Lansinoh is recalling Thera Pearl 3-in-1 Breast Therapy packs because incorrect Spanish heating instructions may cause the product to overheat.
Product
THERA PEARL 3-in-1 BREAST THERAPY, 2 hot and cold packs in plastic box. The Thera Pearl 3-in-1 Breast Therapy is a reusable therapeutic hot and cold pack for use with pain, swelling, engorgement, plugged ducts or mastitis associated with breast feeding or to help encourage l
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0767-2013·2013-02-13
Philips Easy Diagnost Eleva DRF Recalled for Image Marker Misinterpretation
Philips Healthcare is recalling 14 Easy Diagnost Eleva DRF units because a mirror icon on images could be misinterpreted as a right lead marker in PACS systems.
Product
Phillips Easy Diagnost Eleva DRF. Model Number: 706034 Product Usage: Universal Fluoroscopic Applications
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0790-2013·2013-02-13
Remel Recalls Oxoid Aztreonam Antimicrobial Susceptibility Test Discs
Remel Inc is recalling Oxoid Aztreonam test discs because some may lack antibiotic impregnation, potentially affecting test accuracy.
Product
Oxoid Antimicrobial Susceptibility Test Discs, Aztreonam 30 ug, IVD, REF CT0264B, Oxoid Ltd., UK, [email protected] (Both Remel &amp;amp;amp;amp; Oxoid, Ltd are a part of Thermo Fisher Scientific) An antimicrobial susceptibility test disc is a device that consists of
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0765-2013·2013-02-13
Sybron Endo Lightspeed LSX Files Recalled for Incorrect Length Markings
Ormco/Sybronendo is recalling specific lots of Lightspeed LSX endodontic files because their length markings are incorrect.
Product
Sybron Endo Lightspeed: LSX Files, 25MM, Part Numbers: 835-2525; LSX Files, 25MM Assorted Kit, Part Numbers: 835-2455; LSX Files, 30MM, Part Numbers: 835-2031. An engine-driven rotary endodontic instrument used during endodontic procedures for cleaning and shaping the root ca
Category
Medical Device
Distribution
0 states
ModerateFDA (Food)·F-0977-2013·2013-02-13
Mama Tere Barley Flour Recalled for Undeclared Food Dyes
Family Food Distributor, Inc. is recalling Mama Tere Cebada Natural Barley Flour because it contains undeclared food dyes Red #3 and Red #40.
Product
Mama Tere Cebada Natural Barley Flour Net Weight /Peso Neto: 12 oz (340g) Family Food Distributors Bergen Avenue Kearny, NY 07032 UPC 7412003000259
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0983-2013·2013-02-13
Imperial Nuts and Snacks Chocolate and Peanut Platter Recalled for Undeclared Dyes
Star Snacks Co., LLC is recalling Imperial Nuts and Snacks Chocolate and Peanut Platter because it contains undeclared FD&C colors.
Product
Imperial Nuts and Snacks Chocolate and Peanut Platter. Packed By: Star Snacks CO., LLC, Jersey City, NJ 07305. Net Wt. 26 oz (737 g) UPC 5351946762.
Category
Food
Distribution
7 states
ModerateFDA (Devices)·Z-0788-2013·2013-02-13
Exactech Recalls Hip Replacement Liners Due to Labeling Error
Exactech is recalling 26 hip replacement liners because the device labeling was inadvertently transposed. The units were distributed in five states.
Product
Exactech NOVATION CROWN CUP +5mm LATERALIZED LINER, Use with Crown Cup Only, GXL UHMWPE, SN 0123456, REF 136-32-53. Exactech Hip Systems are indicated for use in surgery for hip replacement.
Category
Medical Device
Distribution
5 states
ModerateFDA (Devices)·Z-0787-2013·2013-02-13
Exactech Recalls Novation Crown Cup Hip Liners Due to Labeling Error
Exactech is recalling 26 units of Novation Crown Cup hip replacement liners because device labeling was inadvertently transposed.
Product
Exactech NOVATION CROWN CUP, NEUTRAL LINER, Use with Crown Cup Only, GXL UHMWPE, SN 0123456, REF 130-32-53. Exactech Hip Systems are indicated for use in surgery for hip replacement.
Category
Medical Device
Distribution
5 states
LowFDA (Devices)·Z-0744-2013·2013-02-13
Carestream Recalls Dental Film Due to Missing Label Symbols
Carestream Health is recalling specific lots of Kodak Insight Dental Film because the clear carton labels are missing required symbols and manufacturer information.
Product
KODAK INSIGHT DENTAL FILM in SureSoft Packets, Size 2 Single Packet Film, Model Number IP21S, REF/Catalog Number 8118226 --- COMMON/USUAL NAME: Dental Intraoral Radiographic Film -- 20 cartons of 80 packets. Product Usage: Dental intraoral radiography
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-152-2013·2013-02-13
Sandoz Recalls Syeda Oral Contraceptives for Incorrect Tablet Imprinting
Sandoz is recalling Syeda oral contraceptives because some tablets have the wrong ID imprint. Consumers should stop using the affected lot and contact a healthcare provider.
Product
Syeda (drospirenone and ethinyl estradiol), 3 mg/0.03 mg, 3 x 28 tablet blistercards, combination oral contraceptive tablet, Manufactured by Laboratorios Leon Farma S.A., Spain for Sandoz Inc., Princeton, NJ
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-144-2013·2013-02-13
Stat Rx USA Recalls Methocarbamol Tablets Due to Incorrect Expiration Date
Stat Rx USA is recalling 3 bottles of Methocarbamol 750 mg tablets distributed in Pennsylvania because they were labeled with an incorrect expiration date.
Product
Methocarbamol 750 mg Tablets, 90-count bottle, Mfg by: West-Ward Pharm. Corp., Eatontown, NJ 07724, Packaged and Distributed by: Stat Rx USA, NDC 42549-521-90.
Category
Drug
Distribution
1 state
SevereFDA (Food)·F-0944-2013·2013-02-06
Island Delights Coconut Haystack Candy Recalled for Missing Milk Labeling
Island Delights is recalling Coconut Haystack Candy because the ingredient list failed to disclose milk. The product was distributed to 14 states.
Product
Island Delights Coconut Haystack Candy Maple Natural Flavor Coconut Haystacks, NET WEIGHT 2 OZ, 4 oz and 8 oz clear plastic bags. Bags labeled in part "INGREDIENTS: SUGAR, COCONUT***NATURAL MAPLE FLAVOR***Island Delights, Inc. Seville, OH 44273"
Category
Food
Distribution
14 states
SevereFDA (Devices)·Z-0754-2013·2013-02-06
GE AdvantageSim MD Software Recall for Incorrect Series Labeling
GE Healthcare is recalling AdvantageSim MD versions 7.4 through 7.6 because incorrect series labeling may lead to under-treatment of tumors.
Product
AdvantageSim MD versions 7.4 through 7.6, Model 5160092-2 Version 7.4, 5160092-3 Version 7.5, 5160092-4 version 7.6.
Category
Medical Device
Distribution
13 states
SevereFDA (Food)·F-0963-2013·2013-02-06
Dymatize Elite Protein Bars Recalled for Peanut Allergen Mislabeling
Belmont Confections is recalling Dymatize Elite Gourmet Cookies & Cream protein bars because they contain peanuts but do not list them on the label.
Product
DYMATIZE NUTRITION ELITE Gourmet Cookies & Cream 6-LAYER HI-PROTEIN BAR Label reads in part "NET WT***INGREDIENTS: Elite Protein Blend***Distributed by: Dymatize Enterprises, Inc. 13737 N. Stemmons FWY, Dallas, TX 75234, (888) 334-LEAN or (972) 732-1990.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0948-2013·2013-02-06
Kinnikinnick Frozen Pie Crusts Recalled for Undeclared Egg Allergen
Jerusalem Manufacturing Natural Foods & Wholesalers, Inc. is recalling Kinnikinnick Foods Brand Frozen Pie Crusts because egg is not declared on the label.
Product
Kinnikinnick Foods Brand Frozen Pie Crusts, 290g/10 ounces. 2 crusts per box, 6 boxes per case
Category
Food
Distribution
0 states
HighFDA (Food)·F-0947-2013·2013-02-06
Island Delights Coconut Haystacks Recalled for Missing Milk Allergen Labeling
Island Delights is recalling specific lots of Almond Natural Flavor Coconut Haystacks because the ingredient list failed to disclose the presence of milk.
Product
Island Delights ALMOND Natural Flavor Coconut Haystacks, NET WEIGHT 2 oz, 4 oz, 8 oz and 2 lb clear plastic bags. Bags labeled in part "INGREDIENTS: SUGAR, COCONUT***COCOA***NATURAL COFFEE FLAVOR***Island Delights, Inc., Seville, OH 44273"
Category
Food
Distribution
14 states
HighFDA (Food)·F-0942-2013·2013-02-06
Food Club Chocolate Chunk Brownie Mix Recalled for Undeclared Walnuts
Gilster-Mary Lee Corp. is recalling Food Club Chocolate Chunk Brownie Mix because it contains walnuts that are not listed on the ingredient label.
Product
Food Club Chocolate Chunk Brownie Mix, packaged in 21.5-oz. boxes, UPC# 36800-13486, distributed by TOPCO Associates LLC, Skokie, IL.
Category
Food
Distribution
3 states
HighFDA (Food)·F-0946-2013·2013-02-06
Island Delights Coconut Haystacks Recalled for Undeclared Milk Allergen
Island Delights is recalling Coconut Haystacks because the ingredient list fails to declare milk, a major food allergen.
Product
Island Delights COFFEE NATURAL Natural Flavor Coconut Haystacks, NET WEIGHT 2 oz, 4 oz, 8 oz and 2 lb clear plastic bags. Bags labeled in part "INGREDIENTS: SUGAR, COCONUT***COCOA***NATURAL COFFEE FLAVOR***Island Delights, Inc. Seville, OH 44273"
Category
Food
Distribution
14 states
HighFDA (Food)·F-0945-2013·2013-02-06
Island Delights Coconut Haystacks Recalled for Missing Milk Allergen Labeling
Island Delights, Inc. is recalling specific lots of Coconut Haystacks because the ingredient list failed to disclose milk, a major food allergen.
Product
Island Delights Almond Chocolate/Almond Mix Natural Flavor Coconut Haystacks, NET WEIGHT 2 oz, 4 oz, 8 oz and 2 lb clear plastic bags. Bags labeled in part "INGREDIENTS: SUGAR, COCONUT***COCOA***NATURAL ALMOND FLAVOR***Island Delights, Inc., Seville, OH 44273"
Category
Food
Distribution
14 states
ModerateFDA (Food)·F-0939-2013·2013-02-06
The Father's Table Recalls Vanilla Mini Cake Rolls for Labeling Errors
The Father's Table, LLC is recalling Vanilla Mini Cake Rolls because the labels fail to list strawberries and specific color additives.
Product
Individual packages labeled in part: ***The Bakery baked with pride***Vanilla Mini Cake Roll***8oz**** with strawberry filling*** NETWT 8oz (226g)
Category
Food
Distribution
11 states
ModerateFDA (Food)·F-0936-2013·2013-02-06
General Mills Recalls Betty Crocker Cake Mix for Undeclared Colors
General Mills is recalling a limited quantity of Betty Crocker SuperMoist Golden Vanilla cake mix due to a labeling error involving undeclared FD&C color ingredients.
Product
Betty Croker, Super Moist Cake Mix, Golden Vanilla, NET WT 15.25 oz (432 g), UPC 0 16000 40993 4, Dist by General Mills Sales, Inc., Minneapolis, MN 55440. Case UPC code 1600040993000
Category
Food
Distribution
10 states
ModerateFDA (Food)·F-0938-2013·2013-02-06
The Father's Table Vanilla Rolls Recalled for Missing Allergen Labeling
The Father's Table LLC is recalling Vanilla Rolls because the labels fail to list strawberries and color additives. The FDA classified this as a Class III recall.
Product
Individual packages labeled in part: ***The Father's Table***Vanilla Roll***8oz**** and Master carton labeled in part: "The Father's Table***Shelf Stable*** Mini Vanilla Roll***Contains 12/8oz.***
Category
Food
Distribution
11 states
ModerateFDA (Devices)·Z-0755-2013·2013-02-06
Ortho VITROS Vapor Adsorption Cartridges Recalled for Incorrect Packaging
Ortho-Clinical Diagnostics is recalling VITROS Vapor Adsorption Cartridges because some cartons incorrectly contain Particulate Cartridges, which may bias test results.
Product
Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption Cartridge REF/CAT No. 680 0100. VITROS¿ Vapor Adsorption Cartridges are used to remove vapor contaminants that may potentially interfere with Signal Reagent used with MicroWell Assays on the VITROS¿ 3600, VI
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0746-2013·2013-02-06
Alere Cholestech LDX Multianalyte Control Recalled for HDL Errors
Alere San Diego, Inc. is recalling Alere Cholestech LDX Multianalyte Control kits because they may produce out-of-range HDL cholesterol results.
Product
Alere Cholestech LDX Multianalyte Control, 2 vial set, Catalog Number: 88769 Alere Cholestech LDX Multianalyte Control (hereafter referred to as Controls) enables users to monitor the performance of total cholesterol (TC), high density lipoprotein cholesterol (HDL), triglyceri
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0918-2013·2013-01-30
Conagra Recalls Andy Capp's Cheddar Cheese Fries Due to Unlabeled Soy
Conagra Inc is recalling Andy Capp's Cheddar Cheese Fries because they were packaged in Hot Fries bags that do not list soy as an ingredient.
Product
Andy Capp's Cheddar Cheese Fries packaged in Andy Capp's Hot Fries, 0.85-oz foil bags, snack size, Case UPC: 20-0-26200-47169-7 and Unit UPC: 00-0-26200-47168-6.
Category
Food
Distribution
8 states