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.

76–100 of 9606

  • ModerateFDA (Devices)·Z-2700-2026·2026-07-15

    EMPOWR 3D Knee surgical device recalled due to packaging discrepancy

    Encore Medical, LP is recalling EMPOWR 3D KNEE surgical devices due to a packaging discrepancy where incorrect product sizes were mixed up in packaging.

    Product
    Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product Description: Enovis knee devices are intended for knee arthroplasty.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-2653-2026·2026-07-08

    Covidien Shiley Disposable Decannulation Plug product labeling error

    Covidien LLC is recalling Shiley Disposable Decannulation Plug devices because the product labeling incorrectly indicates the product does not contain DEHP, when in fact the product contains 30 to 35% DEHP.

    Product
    Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the Covidien Shiley Disposable Decannulation Plug are: Product Number / UDI-DI code 4DCFN 10884522006576 4DCFS 10884522006583 4DFEN 10884522006606 6DCFN 10884
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1131-2026·2026-07-01

    Boichik Bagels Whitefish Salad Recalled for Missing Egg Allergen Label

    Boichik Bagels, Inc. is recalling Whitefish Salad because the product labels fail to declare eggs in the allergen statement, despite eggs being present in the mayonnaise ingredient. Consumers with egg allergies who rely on the label may be at risk.

    Product
    boichik bagels Whitefish Salad Ingredients: Smoked whitefish, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-1132-2026·2026-07-01

    Boichik Bagels Tuna Salad recalled for missing egg allergen declaration

    Boichik Bagels Tuna Salad is recalled because the product contains eggs in the mayonnaise ingredient, but the allergen label does not declare eggs as a "contains" allergen.

    Product
    boichik bagles Tuna Salad Ingredients: albacore tuna, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·H-1111-2026·2026-07-01

    Roast beef sandwich incorrectly labeled as turkey and cheddar product

    Produce Innovations is recalling roast beef and cheddar closed-face sandwiches that are labeled as turkey and cheddar. The mislabeling may pose a risk to consumers with turkey allergies.

    Product
    Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhesive label. The label reads in part as "***Lunch Box Kitchen*** Premium Convenience***Turkey & Cheddar Sub***BEST BY 06/14/26 Lot no. 26 134 NET WEIGHT: 6.1oz***KEEP REFRIGERATED*** Produced
    Category
    Food
    Distribution
    4 states
  • ModerateNHTSA·26V411000·2026-06-29

    Jayco Recalls 2024 Alante and Vision RVs for Incorrect Weight Labels

    Jayco is recalling 2024 Alante and Entegra Vision recreational vehicles because the occupant and cargo capacity labels may list incorrect weights, potentially leading to vehicle overloading.

    Product
    JAYCO — JAYCO, ENTEGRA ALANTE, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0951-2026·2026-06-24

    Fairhope Cold Brew Coffee Concentrate Recall Over Missing Refrigeration Label

    Fairhope Roasting Company is recalling its Cold Brew Coffee Concentrate distributed in Alabama for food service because the label is missing a required "Keep Refrigerated" statement.

    Product
    Fairhope Roasting Company Cold Brew Coffee Concentrate, packaged in 1-gallon plastic jugs, UPC 852236006062, for food service only
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·H-0952-2026·2026-06-24

    United Salt Corp Recalls Salt Due to Mislabeling

    United Salt Corp is recalling salt because plain salt was labeled as iodized and iodized salt was labeled as plain, a mislabeling issue.

    Product
    Salt
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·26V397000·2026-06-19

    Indian Motorcycle Recalls 2026 Chief Vintage for Incorrect Rim Labeling

    Indian Motorcycle is recalling 2026 Chief Vintage models because the VIN label lists the wrong rear rim width, which could lead to improper tire mounting and loss of control.

    Product
    INDIAN — INDIAN CHIEF VINTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V385000·2026-06-12

    Winnebago Recalls 2026-2027 Revel Models Due to Incorrect Tire Label

    Winnebago is recalling 2026-2027 Revel and Revel Sport vehicles because the tire information label lists the wrong tire size, which could lead to incorrect replacements and increased crash risk.

    Product
    WINNEBAGO — WINNEBAGO REVEL SPORT, REVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0906-2026·2026-06-10

    Raw Shelled Peanuts Recalled for Undeclared Tree Nut Allergen

    Wilco Peanut Co is recalling raw shelled peanuts (Runner Type) because they may contain undeclared tree nuts, posing an allergen risk to consumers with nut allergies.

    Product
    Raw Shelled Peanuts (Runner Type) 2,200 lb. Poly Tote Bags and 50kg Poly Bags
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0538-2026·2026-05-27

    Atomoxetine Capsules Recalled Due to Labeling Mix-Up Error

    Safecor Health, LLC is recalling Atomoxetine HCl 10 mg capsules because some units are incorrectly labeled as 10 mg when they actually contain 25 mg. Patients taking the mislabeled product may receive an incorrect dose.

    Product
    ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
    Category
    Drug
    Distribution
    1 state
  • ModerateNHTSA·26V342000·2026-05-27

    Tiffin recreational vehicles recalled for incorrect cargo carrying capacity label

    Tiffin is recalling certain 2026–2027 recreational vehicles because the Cargo Carrying Capacity label may have been incorrectly printed on white, making it difficult to locate loading and tire pressure information.

    Product
    TIFFIN — TIFFIN WAYFARER, OPEN TRAIL, MIDAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0535-2026·2026-05-27

    Primidone Tablets Recalled for Cross-Contamination with Acemetacin

    Golden State Medical Supply Inc. is recalling Primidone 250 mg tablets due to cross-contamination with trace amounts of Acemetacin API. The affected lots are distributed nationwide.

    Product
    PRIMIDONE — PRIMIDONE (PRIMIDONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V335000·2026-05-26

    Ford Recalls 2026 Ranger and Bronco for Incorrect Tire Placard Labels

    Ford is recalling 2026 Ranger and Bronco vehicles because tire placards and safety labels may list incorrect specifications, creating a risk of vehicle overload or improper tire inflation.

    Product
    FORD — FORD RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V315000·2026-05-18

    Tesla 2025-2026 Model Y Vehicles Missing Certification Label

    Tesla is recalling certain 2025 and 2026 Model Y vehicles because the certification label may not have been installed. Missing weight information on the label could lead to vehicle overloading and increase crash risk.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0755-2026·2026-05-13

    Loard's Vanilla Ice Cream Recalled for Undeclared Milk

    Loard's Vanilla Ice Cream in 32 oz and 56 oz containers is being recalled because it contains milk that is not listed on the label.

    Product
    Loard's Vanilla Ice Cream - 32 oz; 56 oz
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2078-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps Model DVF4034-25 Instruction Recall

    Katalyst Surgical, LLC is correcting instructions for DEX Ophthalmic Tissue Forceps, Model DVF4034-25. The company has issued a field safety corrective action for the product's instructions for use.

    Product
    DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2075-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps Field Safety Corrective Action Notice

    Katalyst Surgical is issuing a field safety corrective action for DEX Ophthalmic Tissue Forceps (Model DVF4019-25-S) due to instructions for use updates. The recall affects 645 units distributed nationwide in the US and internationally.

    Product
    DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-25-S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2069-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps subject to Field Safety Corrective Action

    Katalyst Surgical, LLC is issuing a Field Safety Corrective Action for instructions for use (IFU) related to DEX Ophthalmic Tissue Forceps (Model DVF4005-23). The corrective action addresses a labeling issue in the product instructions.

    Product
    DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2076-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps require instructions-for-use correction

    Katalyst Surgical is correcting the instructions for use (IFU) for DEX Ophthalmic Tissue Forceps (Model DVF4019-27) and related scissors due to a field safety issue.

    Product
    DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2074-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps recalled for instruction updates

    Katalyst Surgical is issuing a Field Safety Corrective Action for 670 units of DEX Ophthalmic Tissue Forceps (Model DVF4019-25) due to updates required in the instructions for use. The device was distributed worldwide.

    Product
    DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V282000·2026-05-04

    2026 Toyota 4Runner Vehicles Recalled Due to Incorrect Load Capacity Label

    Gulf States Toyota, Inc. is recalling certain 2026 Toyota 4Runner vehicles because the load carrying capacity label is incorrect. This error may lead to improper vehicle loading and increase the risk of a crash.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide