Hazard

Mislabeling recalls

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

What the numbers show

Total: 395
Critical: 20
Severe: 45
Most recent: 2026-07-22

Of the 395 mislabeling recalls we have scored against our rubric, 20 (5%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 45 (11%) 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 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.

326–350 of 395

HighFDA (Food)·F-1687-2022·2022-09-14
Charlie's Brand Spinach Salad With Honey Dijon Dressing Recalled for Undeclared Fish Allergen
Charlie's brand Spinach Salad With Honey Dijon Dressing is recalled due to undeclared fish (anchovy) in the Worcestershire sauce dressing. Consumers with fish allergies are at risk.
Product
Charlie's brand perishable and refrigerated Spinach Salad With Honey Dijon Dressing, item # 028-09048, packaged in a clear hinged container, net weight per container: 6 oz. UPC 0 45009 85415 5. There are 8/6oz. Spinach Salad With Honey Dijon Dressing containers in the Spinach S
Category
Food
Distribution
4 states
ModerateFDA (Devices)·Z-1572-2022·2022-08-31
SteriSpine PS surgical screws recalled for patient label mislabeling
FDA recalls 8 SteriSpine PS multi-axial fenestrated screw kits distributed in Maryland due to incorrect labeling on patient documentation. The patient labels list the wrong screw type, though other labeling and the devices themselves are correct.
Product
SteriSpine PS kit of 2 Multi-Axial Fenestrated Screws, model numbers/REF numbers KITM640, KITM645, and KITM740.
Category
Medical Device
Distribution
1 state
ModerateFDA (Food)·F-1578-2022·2022-08-31
PICS Ground Cinnamon Recalled Due to Mislabeling as Cumin
PICS Ground Cinnamon distributed to Price Chopper stores in Massachusetts is being recalled because the product actually contains cumin but is mislabeled as cinnamon.
Product
PICS Ground Cinnamon NET WT 16 OZ (453g) UPC 4173505270
Category
Food
Distribution
1 state
HighNHTSA·22V643000·2022-08-26
2023 Forest River fifth wheels have incorrect axle rating on placard
Forest River is recalling 2023 Flagstaff and Rockwood fifth wheels because the Federal Placard lists an incorrect axle rating (5,200 lbs instead of 5,000 lbs), which could lead to vehicle overloading and increased crash risk.
Product
FOREST RIVER — FOREST RIVER FLAGSTAFF, ROCKWOOD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1548-2022·2022-08-24
Medical dressing tray mislabeled as latex-free but contains natural rubber latex
Trinity Sterile's IV catheter dressing trays are mislabeled as latex-free despite containing natural rubber latex in component 94-7002, risking allergic reactions in latex-sensitive users.
Product
Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1549-2022·2022-08-24
Medical Dressing Kit Recalled for Mislabeled Latex Content
Wolf-Pak Premium Dressing Kits labeled latex-free are being recalled because a component contains natural rubber latex, posing a risk to people with latex allergies.
Product
Wolf-Pak Premium Dressing Kit with GuardVA Cs/30 Ref: DC5030LF
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1515-2022·2022-08-10
FDA Recalls Vital Honey Supplement Containing Undeclared Tadalafil
The FDA has recalled Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder due to undeclared Tadalafil. The product was distributed in seven states and poses serious health risks.
Product
Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder; 12 sachets-15g
Category
Food
Distribution
7 states
ModerateFDA (Devices)·Z-1491-2022·2022-08-10
Boston Scientific Recalls EkoSonic Endovascular Device Kit for Mislabeling
Boston Scientific is recalling 10 EkoSonic Endovascular Device Kits due to mislabeling. The affected kits were distributed to healthcare facilities in 10 U.S. states.
Product
EkoSonic Kit 135cm, 12cm TZ The EkoSonic Endovascular Device is packaged as a kit that includes both the USC and IC components. They are placed into the respective trays and sealed in a Tyvek pouch. The sealed pouches are placed inside the kit carton (box) and the product la
Category
Medical Device
Distribution
10 states
HighFDA (Food)·F-1438-2022·2022-07-27
Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Allergen
Chuckanut Bay Foods LLC is recalling chocolate cheesecake bites because the label declares sunflower lecithin but the product contains undeclared soy lecithin, a major allergen. Consumers with soy allergies could experience allergic reactions.
Product
Item 34017-12, Chuckanut Bay Cheesecake Bites Chocolate. Perishable - Keep Refrigerated. There are 8 pieces per pack and 12 packs per case. Net wt. per pack 6.4 oz. UPC 6 03812 34017 5. Item 35017-12, Chocolate Cheesecake Bites. Edible brand. Distributed by Wish Foods, LLC. P
Category
Food
Distribution
13 states
HighFDA (Food)·F-1483-2022·2022-07-27
Honeymoons Milk Chocolate Almond Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honeymoons Milk Chocolate Almond candy due to undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. The product was distributed in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Honeymoons Milk Chocolate Almond. PLU Code: 788394 14756 2.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1443-2022·2022-07-27
Cheesecake Bites Recalled for Undeclared Soy Lecithin Allergen
Chuckanut Bay Cheesecake Bites Lemon are being recalled due to undeclared soy lecithin in the product. The label incorrectly lists sunflower lecithin as an ingredient, posing a risk to consumers with soy allergies.
Product
Item 34032-12, Chuckanut Bay Cheesecake Bites Lemon. Perishable - Keep Refrigerated. There are 8 pieces per pack and 12 packs per case. Net Wt. 6.4 oz. UPC 6 03812 34032 8. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CHOCOLATE COMPOUND (sunflower lecithin**
Category
Food
Distribution
13 states
HighFDA (Food)·F-1449-2022·2022-07-27
Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Allergen
Chuckanut Bay Foods LLC is recalling Sharis Strawberry Cheesecake Bites (Lot Code 2C159A2) due to undeclared soy lecithin. The label lists sunflower lecithin when the product actually contains soy lecithin, posing a risk to consumers with soy allergies.
Product
Item 81109-12, Chuckanut Bay Sharis Strawberry Cheesecake Bites. Perishable - Keep Refrigerated. There are 9 pieces per pack and 12 packs per case. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CANE SUGAR, PASTEURIZED CULTURED MILK INGREDIENTS: CANE SUGAR, CR
Category
Food
Distribution
13 states
LowFDA (Devices)·Z-1390-2022·2022-07-27
Erythropoietin Control Product Instructions Contain Incorrect CE Marking
R & D Systems is replacing Instructions for Use (IFU) for Quantikine IVD Erythropoietin Human Serum Controls due to an incorrect CE marking designation that should not appear on the self-certified product.
Product
Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations in human serum and plasma. IFU, Part Number 750095
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1191-2022·2022-07-20
CVS Hydrogen Peroxide Bottles Contain Isopropyl Alcohol Due to Label Mix-Up
CVS Hydrogen Peroxide Topical Solution bottles contain 70% isopropyl alcohol instead of the labeled hydrogen peroxide. The labeling error could lead to misuse and potential harm if consumers use the product as labeled.
Product
HYDROGEN PEROXIDE — HYDROGEN PEROXIDE (HYDROGEN PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1300-2022·2022-07-06
Orthopedic Plates Recalled Due to Incorrect Etching and Mislabeling
One lot of DVR Anatomic distal radius orthopedic plates was incorrectly etched during manufacturing and may have been placed into kits labeled as a different plate model. The affected plates were distributed to healthcare facilities nationwide.
Product
DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anatomical Plate System used for the fixation of fractures and osteotomies involving the distal radius.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1355-2022·2022-06-29
Frozen Giai Phat Shrimp Balls Recalled for Undeclared Egg Allergen
Giai Phat Shrimp Ball packages may contain undeclared egg allergen, posing a risk to consumers with egg allergies. The FDA Class I recall affects 335,401 bags distributed to California, Illinois, and Idaho.
Product
Giai Phat Shrimp Ball NET Wt. 7 oz. (198g) Keep Frozen Open Packaging Before Thawing Item #30108 Ingredients: Shrimp (surimi), Water, Tapioca Flour, Salt, Sugar, Monosodium, Glutamate, Garlic Powder, White Pepper, Baking Powder, Spice, Sesame Oil, and Red #40 Food Color Manu
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1306-2022·2022-06-22
Blue Moose Spinach Artichoke Dip Recalled: Undisclosed Cashew and Soy Allergens
Blue Moose of Boulder, LLC is recalling Blue Moose Spinach Artichoke Parmesan Dip because it contains cashews and soy, which are not listed on the label. Consumers with allergies to these ingredients face serious health risks.
Product
Blue Moose Spinach Artichoke Parmesan Dip, 7 oz. (198g), packed in a square, clear plastic container, six units in a pack, UPC 8 47847 00467 5, Blue Moose of Boulder, LLC, 1733 Majestic Dr., Lafayette, CO 80026. Store under refrigeration 33 - 41 degrees F.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1307-2022·2022-06-22
Butter Buds Non-Dairy Food Ingredient Recalled for Undeclared Milk Allergen
Butter Buds Inc voluntarily recalled Butter Buds 8X Non-Dairy food ingredient due to undeclared milk, which poses a risk to consumers with milk allergies. The product was distributed in seven U.S. states and internationally.
Product
Butter Buds Food Ingredients. Butter Buds 8X Non-Dairy LD, Item 49380. Sample Jars are 8 oz. and l lb. sized. White poly jar with yellow cap
Category
Food
Distribution
7 states
HighFDA (Food)·F-1312-2022·2022-06-22
Pedialyte Strawberry Lemonade Powder Recalled for Undeclared Wheat Allergen
Abbott Laboratories recalls one lot of Pedialyte Strawberry Lemonade powder because dextrose derived from wheat was not declared on the label. Lot code 287112S00.
Product
Pedialyte***Replaces Electrolytes***Great for Kids and Adults***Strawberry Lemonade Natural Flavor with Other Natural Flavor*** 6 0.6 OZ (17g) PACKETS/NET WT. 3.6 OZ (102g)***INGREDIENTS: ANHYDROUSE DEXTROSE, CITRIC ACID, POTASSIUM CITRATE***Manufactured for: Abbott Nutrition, Ab
Category
Food
Distribution
12 states
ModerateFDA (Devices)·Z-1228-2022·2022-06-15
JOBST Compri2 Compression Bandages Recalled for Folding Box Mislabeling
BSN Medical Inc is recalling JOBST Compri2 and Compri2 lite compression bandages because the folding boxes containing the products are mislabeled. The actual products and immediate packaging are correctly labeled.
Product
(1) JOBST Compri2, REF 76271-01, containing 2 components, one plastic-wrapped padding and one plastic-wrapped compression bandage with compression of approximately 40 mmHg packaged into a pouch and then both components are packaged into a folding box. Shipping case contains 10 f
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1133-2022·2022-06-01
INTERTAN 1.5 nail orthopedic implants recalled due to reversed left-right labeling
Smith & Nephew is recalling INTERTAN 1.5 nails because right nails were marked and labeled as left nails, and vice versa. This mislabeling could lead to incorrect surgical placement.
Product
INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1124-2022·2022-06-01
HydroMARK Breast Biopsy Marker Label Mismatch on Patient Documentation
Devicor Medical Products is recalling 90 HydroMARK Breast Biopsy Markers due to mismatched patient labels that incorrectly identify the product model. The small patient label identifies the device as model 4010-05-08-T3, while the correct model is 4010-05-08-T4.
Product
HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0909-2022·2022-04-06
Schwan's Spinach & Artichoke Dip recalled due to product mislabeling
Fairmont Foods is recalling Schwan's Spinach & Artichoke Dip because cartons may contain Chicken & Broccoli instead, creating potential allergen risks.
Product
Schwan's Spinach & Artichoke Dip. Item Number 061353, UPC 10038-68192. Net Wt. 24 oz. (1 lb. 8 oz.) 680g. Contains: 2 Bowls. Keep Frozen. Cook Thoroughly. Spinach and Artichokes blended with cream cheese and sour cream with Parmesan, Mozzarella, and Romano Cheeses. Dist
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0844-2022·2022-04-06
Medical Device Manufacturer Recalls Quality Control Panel for Incorrect Shelf-Life
Microbiologics Inc recalls the Pneumonia (33 Targets) Control Panel due to a shelf-life discrepancy. The product's shelf-life was determined to be 6 months instead of the labeled 18 months.
Product
Pneumonia (33 Targets) Control Panel, unassayed quality control material, containing: Positive Control 1 - Semi-Quantitative Bacteria Positive Control 2 - Viruses and Atypical Bacteria
Category
Medical Device
Distribution
8 states
SevereFDA (Food)·F-0907-2022·2022-03-30
Sprouts Dark Chocolate Covered Cherries Recalled for Undeclared Tree Nuts
Sprouts Farmers Market Dark Chocolate Covered Cherries may contain undeclared almonds. The FDA issued a Class I recall for this undeclared tree nut allergen.
Product
Sprouts Farmers Market Dark Chocolate Covered Cherries; Dried Cherries covered in Rich Dark Chocolate. Net Wt. 12 oz (340g) Item # 638-011 UPC: 6 46670 46342 6 Processed in a facility that processes on shared equipment with peanuts, tree nuts, wheat and milk. Distribu
Category
Food
Distribution
6 states