Hazard

Mis Labeling recalls

9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 9,606
Critical: 160
Severe: 588
Most recent: 2026-09-09

Of the 9,606 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (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.

1051–1075 of 9606

HighFDA (Food)·F-1445-2022·2022-07-27
Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Lecithin
Chuckanut Bay Foods is recalling Dipped Cheesecake Bites Chocolate because the product label lists Sunflower Lecithin when it actually contains undeclared Soy Lecithin, a potential allergen.
Product
Item 39417-12, Chuckanut Bay DIPPED CHEESECAKE BITES Chocolate. Perishable - Keep Refrigerated. There are 4 pieces per pack and 12 packs per case. Net Wt. 3.2 oz. per package. UPC 6 03812 39417 8. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CANE SUGAR, EGGS,
Category
Food
Distribution
13 states
HighFDA (Food)·F-1447-2022·2022-07-27
Chuckanut Bay Cheesecake Bites recalled for undeclared soy allergen
Chuckanut Bay Foods is recalling Dipped Cheesecake Bites (Pumpkin) because the product contains undeclared soy lecithin. The label incorrectly lists sunflower lecithin, creating a health risk for consumers with soy allergies.
Product
Item 39408-12, Chuckanut Bay DIPPED CHEESECAKE BITES Pumpkin. Perishable - Keep Refrigerated. There are 4 pieces per pack and 12 packs per case. Net wt. 3.2 oz per package. UPC 6 03812 39408 6. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, PUMPKIN, CANE SUGAR,
Category
Food
Distribution
13 states
HighFDA (Food)·F-1437-2022·2022-07-27
Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Allergen
Chuckanut Bay Foods LLC is recalling New York Cheesecake Bites because the label declares sunflower lecithin when the product actually contains undeclared soy lecithin, posing a risk to consumers with soy allergies.
Product
Item 32001-56, Chuckanut Bay New York Cheesecake Bites (Milk Compound) BULK. Perishable - Keep Refrigerated. There are 14 pieces per pack and 56 packs per case. Item 34001-12, Chuckanut Bay Cheesecake Bites New York. Perishable - Keep Refrigerated. Net Wt. 6.4 oz. There are
Category
Food
Distribution
13 states
HighFDA (Food)·F-1446-2022·2022-07-27
Chuckanut Bay Lemon Cheesecake Bites Recalled for Undeclared Soy Lecithin
Chuckanut Bay Foods is recalling Lemon Cheesecake Bites because the label declares Sunflower Lecithin when the product actually contains Soy Lecithin. Consumers with soy allergies may unknowingly consume these products and experience allergic reactions.
Product
Item 39432-12, Chuckanut Bay DIPPED CHEESECAKE BITES Lemon. Perishable - Keep Refrigerated. There are 4 pieces per pack and 12 packs per case. Net Wt. 3.2 oz. UPC 6 03812 39432 1. Item 32032-1, Chuckanut Bay Lemon Cheesecake Bites (Dark Compound) BULK. There are 14 pieces pe
Category
Food
Distribution
13 states
HighFDA (Food)·F-1475-2022·2022-07-27
Honey Caramels Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honey Caramels Cinna Honey due to potential undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Affected products were sold at 10 retail locations in Colorado, New Mexico, and Wyoming, as well as nationwide via internet.
Product
Honey Caramels Cinna Honey. Net wt. 5.87 oz. PLU Code: 788394 12404 4. Ingredients: Honey, butter (pasteurized cream & salt), cream, nonfat dry milk, whey, cinnamon oil, beet juice (color), lecithin, algin & agar.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1448-2022·2022-07-27
Chuckanut Bay cheesecake bites recalled for undeclared soy lecithin
Chuckanut Bay Foods is recalling Dipped Cheesecake Bites (Berry) due to undeclared soy lecithin. The label incorrectly lists sunflower lecithin, potentially endangering consumers with soy allergies.
Product
Item 39421-12, Chuckanut Bay DIPPED CHEESECAKE BITES Berry. Perishable - Keep Refrigerated. There are 4 pieces per pack and 12 packs per case. Net wt. 3.2 oz per package. UPC 6 03812 39421 5. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CANE SUGAR, PASTEURIZE
Category
Food
Distribution
13 states
HighFDA (Drugs)·D-1341-2022·2022-07-27
Loud Muscle Science Recalls Unapproved Capsule Product Marketed as Aphrodisia
Loud Muscle Science is recalling Launch Sequence Aphrodisia Capsules because they were marketed without FDA approval. The product was distributed nationwide in the USA and Canada.
Product
Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC Code 661020846957.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1436-2022·2022-07-27
Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Lecithin
Chuckanut Bay Foods is recalling Cheesecake Bites that contain undeclared soy lecithin, listed on the label as sunflower lecithin. Consumers with soy allergies may face serious risk.
Product
Item 38180-12, Chuckanut Bay Cheesecake Bites New York + Chocolate. Perishable - Keep Refrigerated. There are 8 pieces per plastic clamshell pack and 12 packs per case. Net wt. per pack 6.4 oz. UPC 6 03812 38180 2. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***,
Category
Food
Distribution
13 states
HighFDA (Food)·F-1441-2022·2022-07-27
Espresso Cheesecake Bites recalled due to undeclared soy lecithin
Chuckanut Bay Foods is recalling Espresso Cheesecake Bites because the product contains undeclared soy lecithin. The label states sunflower lecithin, but soy—a major allergen—is actually present.
Product
Item 32023-56, Chuckanut Bay Espresso Cheesecake Bites (Dark Compound) BULK. Perishable - Keep Refrigerated. There are 14 pieces per pack and 56 packs per case. Item 35023-12, Espresso Cheesecake Bites. Edible brand. Distributed by Wish Foods, LLC. Perishable - Keep Refrige
Category
Food
Distribution
13 states
HighFDA (Food)·F-1503-2022·2022-07-27
Chicken Breading Recalled Due to Undeclared Wheat Allergen
Belmatt Inc is recalling Targil's Hot Tails Louisiana Crawfish House Chicken Breading (5,083 pounds, Lot 0206102202) due to undeclared wheat. The product was distributed in Louisiana and poses a risk to consumers with wheat allergies.
Product
Targil's Hot Tails Louisiana Crawfish House Chicken Breading packaged in 25lb boxes
Category
Food
Distribution
1 state
HighFDA (Food)·F-1450-2022·2022-07-27
Chocolate Cheesecake Bites Recalled for Undeclared Soy Lecithin
Chuckanut Bay Foods is recalling Chocolate Cheesecake Bites because the label lists Sunflower Lecithin when the product actually contains Soy Lecithin, an undeclared allergen. Consumers with soy allergies face a potential health risk.
Product
Item 32017-56, Chocolate Cheesecake Bites BULK. Perishable - Keep Refrigerated. There are 14 pieces per pack and 56 packs per case. Firm did not provide label.
Category
Food
Distribution
13 states
ModerateFDA (Devices)·Z-1386-2022·2022-07-27
Stryker Trevo Trak 21 Microcatheter recalled for missing carton product illustration
Stryker Neurovascular is recalling 71 Trevo Trak 21 Microcatheter units because the product carton label is missing the required product drawing or illustration.
Product
Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK - CE, REF: 91413; TREVO NXT 4X41+TRAK21 2-PACK - CE, REF: 91414; TREVO NXT 6X37+TRAK21 2-PACK - CE, REF: 91415; TREVO NXT 4X28+TRAK21+CAT6 3-PACK - CE, REF:
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1393-2022·2022-07-27
NeuRx Diaphragm Pacing System Labeling Revised for Storage Clarity
Synapse Biomedical revised labeling for the NeuRx Diaphragm Pacing System to clarify that temperature range symbols indicate storage conditions, not transport or package conditions. The revision affects 71 units distributed in the United States.
Product
NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036 NeuRx Diaphragm Pacing System, Patient Kit, SCI 20-0028 NeuRx DPS Surgical Kit, HDE 20-0040 NeuRx Diaphragm Pacing S
Category
Medical Device
Distribution
19 states
HighNHTSA·22V532000·2022-07-22
Thomas Built Buses Minotour Recalled for Incorrect Tire Labeling
Daimler Trucks North America is recalling 2019-2023 Thomas Built Buses Minotour school buses because tire labels list the wrong size, potentially affecting vehicle stability.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR SRW
Category
Vehicle
Distribution
Distributed nationwide
ModerateNHTSA·22V521000·2022-07-21
Cruiser Recalls 2022 Shadow Cruiser Travel Trailers Due to Incorrect Weight Label
Cruiser RV is recalling 2022 Shadow Cruiser travel trailers because the federal certification label displays the incorrect Gross Axle Weight Rating, which may allow the vehicle to be overloaded.
Product
CRUISER RV — CRUISER RV SHADOW CRUISER
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1188-2022·2022-07-20
Morphine Sulfate Extended-Release Tablets Recalled for Strength Label Mix-up
Bryant Ranch Prepack has recalled Morphine Sulfate extended-release tablets due to a label mix-up where bottles may contain the wrong strength. Contact your pharmacy to verify your correct dose.
Product
Morphine Sulfate extended-Release Tablets, USP; 60 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories Inc., NJ; Relabeled by: Bryant Ranch Prepack, Inc, CA, NDC 63629-1089-01
Category
Drug
Distribution
1 state
SevereUSDA FSIS·022-2022·2022-07-20
Knorr Curry Chicken and Rice Soup Mix Recalled for Undeclared Milk
MSI Express Inc. is recalling Knorr Curry Chicken and Rice Soup Mix because it contains undeclared milk, a known allergen.
Product
MSI Express Inc. Recalls Unilever Food Solutions U.S. Knorr Curry Chicken and Rice Soup Mix Products Due to Misbranding and Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1187-2022·2022-07-20
Morphine Sulfate Tablets Recalled for Label Mix-up Dosage Error
Morphine Sulfate extended-release tablets (30 mg) distributed in Alabama were recalled due to a critical label mix-up where bottles labeled as 60 mg contain 30 mg, and bottles labeled as 30 mg may contain 60 mg.
Product
Morphine Sulfate extended-Release Tablets, USP; 30 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories Inc., New Brunswick NJ 08901 USA; Relabeled by: Bryant Ranch Prepack, Inc., Burbank, CA, 91504 USA, NDC: 63629-1088-01.
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-1384-2022·2022-07-20
Anti-FITC-AP CISH Kit Label Bears Incorrect Expiration Date
Agilent Technologies is recalling 63 Anti-FITC-AP CISH Accessory Kits due to incorrect expiration dates on substrate vial labels, which may result in the use of expired materials.
Product
Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-21 Vial Labels: Mat. No K589911-21512
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1361-2022·2022-07-20
Medical device manufacturer recalls mislabeled interference screws nationwide
SCIENCE & BIO MATERIALS has recalled ComposiTCP 30 Interference screws due to mislabeling. The recall affects 72 units distributed nationwide in the US.
Product
ComposiTCP 30 Interference screw D 7- L:25 mm, REF 110004605
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1338-2022·2022-07-13
Rayner RayOne Intraocular Lens Systems Mislabeled with Incorrect Lens Strength
Rayner is recalling RayOne intraocular lens injection systems because the outer package is mislabeled and contains a different lens strength than indicated. Approximately 162 devices were distributed in 13 US states.
Product
RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one MICS injection system with Intraocular Lens: (1) Outer carton labeled as Rayner RayOne EMV US, REF RAO200E, SE: +19.00D, Sph: +19.00D; and (2) Inner primary device packaging labeled as Rayner RayOne EM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1323-2022·2022-07-13
EIT CIF Cage Intervertebral Fusion Device Carton Labeling Mismatch Recall
DePuy Spine is recalling 61 units of the EIT CIF cage spinal fusion device due to a labeling mismatch. The outer carton label does not match the labels on the blister packages and patient information labels.
Product
EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD). Part Number: CUI8060L
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-07122022-01·2022-07-12
Trader Joe's Caesar Salad with Chicken Alert for Undeclared Egg Allergen
USDA issued a public health alert for Trader Joe's Caesar Salad with Chicken because the dressing packets contain undeclared egg. No illnesses have been reported.
Product
F&S Produce West LLC — FSIS Issues Public Health Alert for Ready-to-Eat Caesar Salad with Chicken Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-07072022-01·2022-07-07
USDA Issues Public Health Alert for Uninspected Rendered Pork Fat Products
USDA FSIS issued a public health alert for Don Panchito rendered pork fat produced without federal inspection. No illnesses have been reported, but consumers should discard the product.
Product
FSIS Issues Public Health Alert for Rendered Pork Fat Products Produced without the Benefit of Federal Inspection
Category
Food
Distribution
1 state
HighFDA (Food)·F-1387-2022·2022-07-06
PurAqua Belle Vie Sparkling Water Recalled for Undeclared Caffeine
PurAqua Belle Vie Sparkling Water with Ashwagandha contains undeclared caffeine. The product was distributed to 17 states and poses potential risk for caffeine-sensitive consumers.
Product
PurAqua Belle Vie SPARKLING WATER wellness RELAX 100mg ASHWAGANDHA PER 12 FL OZ STRAWBERRY CUCUMBER FLAVORED SPARKLING WATER WITH OTHER NATURAL FLAVORS 12 FL OZ (355mL) CAN UPC: 4099100315622
Category
Food
Distribution
17 states