The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 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.

2926–2950 of 9607

  • HighFDA (Food)·F-1189-2019·2019-03-20

    Hikari Miso Recalled for Missing English Soy Allergen Labeling

    Hikari Miso International is recalling Hikari Enjuku Koji Miso Mutenka because the product lacks English labeling, failing to declare soy as an allergen.

    Product
    Hikari Enjuku Koji Miso Mutenka; 26.6 oz. plastic tub with lid. UPC 4 905663 003007
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1216-2019·2019-03-20

    JOY Tamarind and Dates Chutney Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling Tamarind and Dates Chutney because it contains undeclared sulfites. The product was distributed in Connecticut, New York, and New Jersey.

    Product
    JOY Tamarind and Dates Chutney (SWEET N' SOUR SAUCE), NET WT 8 OZ (228g), UPC: 6 80617 60437 4 and NET WT: 16 OZ (456g), UPC: 6 80617 60438 1 and NET WT 32 OZ (907g), UPC: 6 80617 60022 2
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1005-2019·2019-03-20

    Zimmer NexGen Trabecular Metal Tibial Augment Recall for Label Mismatch

    Zimmer Trabecular Metal Technology is recalling 24 units of NexGen Tibial Half Block Augments because the product in the box may not match the label.

    Product
    NexGenTrabecular Metal Tibial Half Block Augment, Right Lateral/Left Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800426 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the kne
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1000-2019·2019-03-20

    Ossur CB Resolve Halo System Recalled for Labeling and Testing Issues

    Ossur Americas is recalling 656 units of CB Resolve Halo system products due to a labeling error and the need for confirmatory safety testing.

    Product
    Ossur CB Resolve, Sterile, Part/ Description: 505300C/ CB RESOLVE STERILE UNIT SML; 505400C/ CB RESOLVE STERILE UNIT STD; 505500C/ CB Resolve Sterile Unit LRG; 515300C/ CB RESOLVE RING KIT SM-No App; 515400C/ CB RESOLVE RING KIT STD-No App; 515500C/ CB RESOLVE RING KIT
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1003-2019·2019-03-20

    Ossur ReSolve Halo Vest Recalled for Labeling and Safety Testing Issues

    Ossur Americas is recalling 381 ReSolve Halo Vests because the titanium pin label incorrectly lists a ceramic tip and the products require confirmatory safety testing.

    Product
    Ossur, ReSolve Halo Vest, Part/ Description: 545700K/ ReSolve Halo Vest-shrt kodel; 545700L/ ReSolve Halo Vest-shrt lmbwool; 545800K/ ReSolve Halo Vest-tall kodel; 545800L/ ReSolve Halo Vest-tall lmbwool
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Drugs)·D-1012-2019·2019-03-20

    Medtech Recalls Little Remedies New Baby Essentials Kit for Labeling Errors

    Medtech Products is recalling 4,716 Little Remedies New Baby Essentials Kits because the cartons contain incorrect labeling for two of the five items inside.

    Product
    Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following products: Little Remedies Infant Fever Reducer (acetaminophen 150mg) 2 fl. oz. bottle, Little Remedies Saline Spray/Drops (sodium chloride) 0.5 fl oz., Little Remedies Gripe Water (zingiber officin
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1001-2019·2019-03-20

    Ossur Halo System Ring Kits Recalled for Labeling and Safety Testing

    Ossur Americas is recalling 182 units of Halo system ring kits due to a labeling error and the need for confirmatory safety testing.

    Product
    Ossur, Sterile, Part/ Description: 505300T/ CB RING KIT TI SM; 505300V2/ OB V2 RING KIT TI SM; 505400T/ CB RING KIT TI STD; 505400V2/ OB V2 RING KIT TI STD; 505500T/ CB RING KIT TI LG; 505500V2/ OB V2 RING KIT TI LG; 515300V2/ OB V2 RING KIT TI SM-No App; 515400V2/ OB
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1004-2019·2019-03-20

    Ossur LIL Angel Vest Recalled for Labeling and Safety Testing Issues

    Ossur Americas is recalling 45 LIL Angel Vests because the titanium pin labels incorrectly list ceramic tips and require confirmatory safety testing.

    Product
    Ossur, LIL Angel Vest, Part/ Description: 545100K/ LIL ANGEL VEST P2 KODEL; 545100L/ LIL ANGEL VEST P2 LAMBSWOOL; 545100S/ LIL ANGEL VEST P2 SORBATEX; 545150K/ LIL ANGEL VEST P3 KODEL; 545150L/ LIL ANGEL VEST P3 LAMBSWOOL; 545150S/ LIL ANGEL VEST P3 SORBATEX
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1002-2019·2019-03-20

    Ossur J Tong Sterile Medical Device Recall for Labeling Error

    Ossur Americas is recalling 138 units of J Tong sterile medical devices because the titanium pin label incorrectly lists a ceramic tip.

    Product
    Ossur, J Tong, Sterile, Part/ Description: JT-115/ J TONG MED/LGE-No App; JT-200/ J TONG ASSEMBLY SML/MED; JT-210/ J TONG ONLY SML/MED; JT-400/ J TONG COMPONENT TRAY
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-0998-2019·2019-03-20

    Ossur Skull Pin Recall for Labeling Error and Safety Testing

    Ossur Americas is recalling 824 sterile skull pins due to a label error and pending safety testing.

    Product
    Ossur Skull Pin, Sterile Ceramic Tip Pin, Part/ Description: 516CS/ Skull Pin 2-1/4in CT Sterl 1PK; 516DS/ Skull Pin 3in CT Sterl 1PK; 517CS/ Skull Pin 2-1/4in CT Sterl 4PK; 517DS/ Skull Pin 3in CT Sterl 4 PK; 522CS/ Skull Pin 2-1/4in CT Sterl 6PK; 522C/ SKULL PIN 2-1/4
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-0997-2019·2019-03-20

    Ossur Skull Pin Recall Due to Labeling Error and Safety Testing

    Ossur Americas is recalling 372 sterile titanium skull pins because the label incorrectly lists a ceramic tip and the products require confirmatory safety testing.

    Product
    Ossur Skull Pin, Sterile Titanium Pin, Part/Description: 516TS/ Skull Pin 2-1/4in TI Sterl 1PK; 516V2S/ Skull Pin 3in TI Sterl 1PK; 520TS/ Skull Pin 2-1/4in TI Sterl 5PK; 520V2S/ Skull Pin 3in TI Sterl 5 PK
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-0999-2019·2019-03-20

    Ossur OB Resolve Sterile Ring Kits Recalled for Labeling Errors

    Ossur Americas is recalling 342 units of OB Resolve sterile ring kits due to a labeling error on titanium pins and pending safety testing.

    Product
    Ossur OB Resolve, Sterile, Part/ Description: 505300D/ OB RESOLVE STERILE RING SML; 505400D/ OB RESOLVE RING KIT STD; 505500D/ OB RESOLVE RING KIT LRG; 515300D/ OB RESOLVE RING KIT SM-No App; 515400D/ OB RESOLVE RING KIT STD-No App; 515500D/ OB RESOLVE RING KIT LG-No Ap
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Food)·F-1143-2019·2019-03-13

    Meijer Recalls Chocolate Mint Chip Cookies Due to Undeclared Soy

    Meijer is recalling specific lots of Ultimate Chocolate Mint Chip Cookies because they contain undeclared soy. The recall covers products sold in Meijer stores nationwide.

    Product
    Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic clamshell 12 count UPC 4125014563 20 count UPC 4125014564
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1147-2019·2019-03-13

    Good Neighbor Pharmacy Vitamin D Supplement Recalled for Mislabeling

    Twenty-First Century Healthcare is recalling Good Neighbor Pharmacy Vitamin D 2000 IU tablets because they are mislabeled and may contain Co Q10.

    Product
    Good Neighbor Pharmacy, D 2000 IU, Dietary Supplement, UPC: 0-87701-40751-2, 30 tablets.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1152-2019·2019-03-13

    Gasco Golden Egg Yellow Food Color Recalled for Undeclared Ingredients

    Gasco Industrial is recalling Golden Egg Yellow Shade Food Color because the label fails to declare Yellow #5 and potassium sorbate.

    Product
    Gasc¿ Golden Egg Yellow Shade Food Color, Contains: 32 fl. oz. (946 mL)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1146-2019·2019-03-13

    Good Neighbor Pharmacy Co Q10 Capsules Recalled for Mislabeling

    Twenty-First Century Healthcare is recalling Good Neighbor Pharmacy Co Q10 200mg capsules because they are mislabeled and may contain Vitamin D.

    Product
    Good Neighbor Pharmacy, Co Q10 200mg Capsule, Dietary Supplement, UPC: 0-87701-40817-5, 30 capsules.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0982-2019·2019-03-13

    Cepheid Respiratory Control Panel Recalled for Reduced Expiration Date

    Microbiologics Inc is recalling Cepheid Respiratory Control Panels because the expiration date was reduced from 24 months to 13 months.

    Product
    Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1153-2019·2019-03-13

    Gasco Tomato Red Food Color Recalled for Undeclared Yellow #6

    Gasco Industrial is recalling Tomato Red Food Color because it fails to declare Yellow #6, a food additive.

    Product
    Gasc¿ Tomato Red Food Color, Net Contents: 5 gal (640 fl. oz)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0980-2019·2019-03-13

    Stryker Recalls T2 Basic Long Instrument Sets Due to Mislabeling

    Stryker GmbH is recalling 17 T2 Basic Long Instrument Sets because faceplates may incorrectly identify them as T2 Basic Short sets.

    Product
    Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Drugs)·D-0994-2019·2019-03-13

    Petra Hygienic Systems Recalls Athleticare Hand Soap Due to Triclosan

    Petra Hygienic Systems is recalling Athleticare Anti-Bacterial Hand Soap because it contains triclosan, an ingredient no longer permitted in over-the-counter antiseptic wash products.

    Product
    ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan), 0.25%, 4 litres/1.1 US Gallon bottles, packaged in 4 x 4 Litres/1.1 US gallons per case, Petra Hygienic Systems, Concord, ON L4K 4RS/ Reno, NV 89511, NDC 42326-550-01, UPC 0 65936 10335 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·028-2019·2019-03-12

    North Country Smokehouse Recalls Pork Sausage Due to Gluten Misbranding

    North Country Smokehouse is recalling approximately 9,000 pounds of pork banger sausage because the product contains wheat despite a gluten-free claim.

    Product
    North Country Smokehouse — North Country Smokehouse Recalls Pork Sausage Products Due to Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·027-2019·2019-03-12

    Carnivore Meat Company Recalls Beef and Pork Sausage Due to Undeclared Soy

    Carnivore Meat Company is recalling approximately 379 pounds of raw beef and pork sausage products because they contain undeclared soy, a known allergen.

    Product
    LSI Specialty Meats — Carnivore Meat Company, LLC Recalls Beef and Pork Sausage Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • CriticalUSDA FSIS·026-2019·2019-03-11

    Choice Canning Recalls Chicken Fried Rice for Undeclared Milk Allergen

    Choice Canning Company is recalling approximately 35,459 pounds of FUSIA Chicken Fried Rice products because they contain milk, a known allergen, that is not declared on the label.

    Product
    Choice Canning Company Inc. — Choice Canning Company, Inc. Recalls Chicken Fried Rice Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    9 states
  • SevereUSDA FSIS·025-2019·2019-03-09

    Conagra Recalls Chef Boyardee Bowls Due to Undeclared Allergens and Misbranding

    Conagra Brands is recalling specific Chef Boyardee rice bowls that contain undeclared milk and wheat allergens and are mislabeled as beef ravioli.

    Product
    Hometown Food Company — Conagra Brands, Inc. Recalls Chicken and Rice Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states