The Recall Desk

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.

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.

1101–1125 of 9606

  • SevereFDA (Food)·F-1270-2022·2022-06-15

    Trader Joe's Lemony Arugula Basil Salad Kit recalled for undeclared egg and wheat allergens

    Taylor Farms is recalling Trader Joe's Lemony Arugula Basil Salad Kit for undeclared egg and wheat allergens. Affected consumers should not consume the product.

    Product
    Trader Joe's Lemony Arugula Basil Salad Kit Arugula, carrots, almonds, and parmesan cheese with a basil lemon vinaigrette NET WT. 9.75 OZ (276g)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1166-2022·2022-06-15

    Diced Potatoes Recalled Due to Undeclared Sodium Metabisulfite

    Liberty Fruit Co is recalling diced potatoes because sodium metabisulfite, a food preservative, is not declared on the product label. Food service locations in Kansas, Nebraska, Iowa, and Missouri are affected.

    Product
    POTATO 1/4" DICE 4/5# C/C (01)10886810715535(10)0016088723 71553 Best if used by: 04/06/22 Ingredients: Potato, Sodium Metabisulfite
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1237-2022·2022-06-15

    Triathlon Tritanium Tibial Components Recalled for Size-Packaging Mismatch

    Howmedica Osteonics is recalling specific lots of Triathlon Tritanium Tibial Components (knee implants) due to a potential mismatch between package labeling and the actual component size contained inside.

    Product
    Triathlon Tritanium Tibial Component (Size 6); Catalog Number 5536-B-600 Triathlon¿ Tritanium¿ Tibial Component (Size 5); Catalog Number 5536-B-500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1239-2022·2022-06-15

    Oakworks Emergency Field Bed Recalled for Incorrect Weight Capacity Label

    Oakworks has recalled 109 units of its Emergency Field Bed due to an incorrect weight capacity label. The label states 500 lbs, but the bed's actual weight limit is 400 lbs.

    Product
    Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1238-2022·2022-06-15

    Emergency relief bed recalled for missing UDI and incorrect weight limit label

    Oakworks Inc is recalling PX200 Emergency Relief Beds due to labeling defects. The product label is missing the UDI number and states an incorrect weight capacity of 500 lbs instead of the actual 400 lb limit.

    Product
    PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1154-2022·2022-06-15

    Dietary supplement gummies recalled for potential undeclared gluten

    Supple Bears Quercetin Bromelain Gummies are recalled because they are labeled as gluten-free but may contain gluten. Consumers with celiac disease or gluten sensitivity should not use this product.

    Product
    SUPPLE BEARS QUERCETIN BROMELAIN GUMMIES + Vitamin C & Zinc 60 DIETARY SUPPLEMENTS NO SOY, NO GLUTEN, NO EGGS, NO DIARY, NO NUTS, NO GELATIN, NO ARTIFICIAL COLOR, FLAVOR OR SWEETENER, NO PRESERVATIVES. Dist. & Sold Exclusively By: SuppleBears 14311 Reese Blvd STE Huntersville, No
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-1258-2022·2022-06-15

    Trader Joe's Southwestern Chopped Salad Recalled for Undeclared Pistachio Allergen

    Trader Joe's Southwestern Chopped Salad is recalled because it contains an incorrect master pack with undeclared pistachio allergen. Consumers with pistachio allergies should not consume this product.

    Product
    Trader Joe's Southwestern Chopped Salad Contains: Green Cabbage, Romaine, Cotija Cheese, Roasted Pepitas, Tortilla Strips, Green Onion, Cilantro, and a spicy Southwest Avocado Dressing Best if used by: May 26, 2022 Perishable, Keep Refrigerated Product of USA-Mexico Romaine: Sali
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1273-2022·2022-06-15

    Zydot Ultimate Blend Detox Drink Recalled for Undeclared Food Coloring and Preservatives

    Zydot Unlimited recalls its Ultimate Blend detox drink due to undeclared food colorings (Y5 and R40) and preservatives on the label. Consumers with allergies to these ingredients should not use the product.

    Product
    Zydot Ultimate Blend The Original Detox Drink Natural Orange Flavor 16 fl. oz. (473 ml) UPC packaged in plastic bottle with lid
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1271-2022·2022-06-15

    Detox drink recalled for undeclared preservatives and food coloring

    Zydot Ultimate Blend The Original Detox Drink is recalled for undeclared preservatives (potassium sorbate, sodium benzoate) and food coloring R40. The recall involves 1,150 bottles distributed in the USA.

    Product
    Zydot Ultimate Blend The Original Detox Drink Natural Cherry Flavor 16 fl. oz. (473 ml) UPC 754515281439 packaged in plastic bottle with lid
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1235-2022·2022-06-15

    Biliary Electrohydraulic Lithotripter Probe Recalled for Incorrect Product Labeling

    Northgate Technologies is recalling 55 AUTOLITH Touch 1.9F biliary lithotripter probes due to incorrect product labeling. Affected devices were distributed nationwide in Massachusetts.

    Product
    AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1131-2022·2022-06-08

    Dierbergs Kitchen spiral pasta salad mislabeled; undeclared egg allergen

    Dierbergs Kitchen Fresh Garden Spiral Pasta Salad is mislabeled as Garden Spiral Pasta but actually contains Broccoli Cheddar Pasta, which contains undeclared egg allergen. Consumers with egg allergies should not consume this product.

    Product
    Dierbergs Kitchen Fresh Garden Spiral Pasta Salad Size: 12oz and 2 lb UPC: 231145703543 Sell By May 31, 22 Sell By Date: 05/31/22 Fresh Garden Spiral Pasta Salad Size: 2LB Family Pack UPC: 231145311625 Sell By Date: 05/31/22
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1135-2022·2022-06-08

    Delta 8 Gummy Edibles Recalled for Undeclared Soy and Coconut Allergens

    TWISTED BRANDS LLC is recalling Cosmic Crunch Bites By Twisted Delta 8 edibles due to undeclared soy lecithin and coconut oil, which may pose a serious allergy risk to consumers with these allergies.

    Product
    Cosmic Crunch Bites By Twisted, Delta 8 1000mg 25 mg per piece, 40 pieces 446g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1132-2022·2022-06-08

    Cherry Coca-Cola Zero Sugar Recalled for Undeclared Phenylalanine

    Cherry Coca-Cola Zero Sugar in 12 oz cans were mislabeled as regular Cherry Coca-Cola and failed to declare phenylalanine on the label, a concern for people with phenylketonuria.

    Product
    Cherry Coca-Cola Zero Sugar Case UPC: 0 49000 04751 6 12 pack fridge pack Single 12 oz. cans if sold individually from the fridge pack.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1094-2022·2022-06-08

    Potato-Cheddar-Jalapeno Pierogi Recalled for Undeclared Milk Allergen

    Grandma's Cuisine Potato-Cheddar-Jalapeno Pierogi is recalled for containing undeclared milk, an allergen. The product was distributed to retailers and restaurants in New Jersey, Massachusetts, and Pennsylvania.

    Product
    Potato-Cheddar-Jalapeno Pierogi Grandma s Cuisine Potato-Cheddar-Jalapeno Pierogi UPC: 8 67355 00043 3 16 oz (454g) / 1 dozen
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1208-2022·2022-06-08

    Bio-Rad Sickle Cell Testing Software CD-ROM Defect Overwrites Custom Settings

    Bio-Rad is recalling Resin Update CD-ROM software (Model 250-3020) for the VARIANT nbs Sickle Cell Program because the update procedure overwrites custom laboratory settings, potentially causing incorrect pattern assignment in tested samples.

    Product
    Resin UPDATE CD-ROM, REF: 250-3020 inside VARIANTnbs Sickle Cell Program Reorder Pack, REF: 250-3000
    Category
    Medical Device
    Distribution
    24 states
  • ModerateFDA (Devices)·Z-1213-2022·2022-06-08

    Abbott FIRMap Catheter Recalled for Incorrect Product Labeling

    Abbott is recalling 40 units of FIRMap® Catheter, 60mm Basket due to incorrect product labeling. The recall affects devices distributed in Missouri, California, Ohio, Washington and internationally in Italy and Netherlands.

    Product
    FIRMap" Catheter, 60mm Basket
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1079-2022·2022-06-01

    Spicy Chicken Sauce recalled due to undeclared wheat allergen

    Joonsung Trading Inc is recalling Spicy Chicken Sauce in 1/2 gallon plastic jugs because the product contains wheat but the label does not declare it. This poses a serious risk to consumers with wheat allergies.

    Product
    Spicy Chicken Sauce packaged in 1/2 gallon plastic jug. Label read in parts "Ingredient: Soy sauce (Gluten free), Sugar, Korean hot bean paste, Garlic powder, Ginger powder, Mirin, Korean hot pepper, Sambal hot sauce"
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1088-2022·2022-06-01

    Mrs. Miller's Homemade Jam Recalled for Undeclared Soy Allergen

    Mrs. Miller's Homemade Jam Smokey BBQ Bacon Jam is being recalled because the label does not declare soy allergen. 5,315 cases were distributed across 15 states.

    Product
    Mrs. Miller's Homemade Jam Smokey BBQ Bacon Jam packaged into 9 oz glass jar 12 jars per case
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1089-2022·2022-06-01

    Mrs. Miller's Homemade Jam Spicy Chili Bacon Jam recalled for undeclared soy allergen

    Mrs. Miller's Homemade Jam Spicy Chili Bacon Jam is being recalled for undeclared soy allergen. The product was distributed across 15 U.S. states. Consumers with soy allergies should not consume it.

    Product
    Mrs. Miller's Homemade Jam Spicy Chili Bacon Jam packaged into 9 oz glass jar 12 jars per case
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Drugs)·D-0890-2022·2022-06-01

    Vegan Lip Balm Recalled Due to Active Ingredient Mislabeling

    Higher Education Make Out Ready Vegan Lip Balm is recalled due to mislabeling of active ingredients. The label does not match the product's actual sunscreen actives.

    Product
    Higher Education Make Out Ready Vegan Lip Balm, SPF 15, Net Wt. 0.15 oz (4.25 g) per tube, Active Ingredients: Oxtinoxate (7.5%), Oxybenzone (3%); Distributed by: Higher Education Skincare, 1.833.251.0388
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1123-2022·2022-06-01

    Benzphetamine tablets recalled due to label mix-up with Benzonatate

    Calvin Scott & Company recalled Benzphetamine 50mg tablets due to a labeling error where bottles labeled as Benzonatate 100mg capsules contained Benzphetamine 50mg tablets and vice versa. One physician in Alpharetta, Georgia received 13 affected bottles.

    Product
    Benzphetamine tablets, 50mg, CIII, repackaged in 30-count bottles, Distributed by Calvin Scott & Co., Inc, Albuq., NM. 87123, NDC 10702-0040-50
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0896-2022·2022-06-01

    Drug Recall: Tivicay Tablets with Incorrect Expiration Date on Label

    GlaxoSmithKline is recalling 328 bottles of Tivicay (dolutegravir) tablets nationwide due to incorrect expiration date labeling. The label shows January 2027 but the correct expiration date is September 2026.

    Product
    TIVICAY — TIVICAY (DOLUTEGRAVIR SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1125-2022·2022-06-01

    Medical device labeling error: KWIK-STIK® plus Clostridium perfringens

    Microbiologics Inc recalled 8 units of KWIK-STIK® plus Clostridium perfringens due to a labeling error. The affected lot (801-44-4) was distributed to laboratories in the United States and internationally.

    Product
    KWIK-STIK" plus: Clostridium perfringens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V384000·2022-05-27

    Ford F-Series and E-Series Vehicles Missing Tire Information on Safety Labels

    Ford is recalling certain 2022 F-Series and 2023 E-Series vehicles whose Safety Certification Labels are missing tire size, rim type, and pressure values. The missing information could lead to incorrect tire selection or pressure, increasing crash risk.

    Product
    FORD — FORD F-250 SD, E-250, E-150, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1106-2022·2022-05-25

    HeartWare Ventricular Assist Device recalled for translation errors

    Heartware, Inc. is recalling the HeartWare Ventricular Assist Device (HVAD) in Finland and Turkey due to translation errors in device displays and supporting documentation that could impair proper device operation.

    Product
    HeartWare Ventricular Assist Device (HVAD) System, Model Number 1521DE, MONITOR 1521DE EXPLORE TECH
    Category
    Medical Device
    Distribution
    0 states