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.

2676–2700 of 9607

  • ModerateFDA (Devices)·Z-1881-2019·2019-07-03

    Medtronic Mosaic 310 Bioprosthesis Recalled for Incorrect Size Labeling

    Medtronic is recalling 15 Mosaic 310 Bioprosthesis mitral valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.

    Product
    Mosaic 310 Bioprosthesis, Mitral, REF 310C31 - Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1882-2019·2019-07-03

    Medtronic Hancock II Mitral Bioprosthesis Recalled for Incorrect Size Labeling

    Medtronic is recalling 15 Hancock II T510 Mitral Bioprosthesis valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.

    Product
    Hancock II T510 Bioprosthesis, Mitral, REF T505U227 - Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1883-2019·2019-07-03

    Medtronic Hancock II T510 Bioprosthesis Recalled for Incorrect Size Labeling

    Medtronic is recalling 15 Hancock II T510 Bioprosthesis valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.

    Product
    Hancock II T510 Bioprosthesis, Mitral, REF T510C27 - Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1884-2019·2019-07-03

    Medtronic Hancock II T510 Bioprosthesis Recalled for Incorrect Size Labeling

    Medtronic is recalling 15 Hancock II T510 Bioprosthesis mitral valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.

    Product
    Hancock II T510 Bioprosthesis, Mitral, REF T510C27 - Product Usage: Replacement of malfunctioning native or prosthetic aortic and/or mitral valves.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V503000·2019-06-28

    Toyota Recalls 2017-2019 Models for Incorrect Load Capacity Label

    Toyota is recalling 2017-2019 Camry, Corolla, RAV4, Sienna, and Yaris iA vehicles because an incorrect load capacity label may lead to unintentional overloading.

    Product
    TOYOTA — TOYOTA RAV4, CAMRY, SIENNA, YARIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1490-2019·2019-06-26

    Whole Foods Sun-Dried Tomato Pesto Recalled for Undeclared Allergens

    Whole Foods Market is recalling sun-dried tomato pesto because the labels failed to declare milk, walnuts, and pine nuts.

    Product
    Sun-dried tomato pesto, sold by weight in plastic deli containers PLU code beginning with 256009
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1484-2019·2019-06-26

    Frozen Japanese Chocolate and Walnut Product Recalled for Undeclared Coconut

    Wismettac Asian Foods is recalling 40 units of Monaka Belgium Choco & Kurumi Daiichi F in California because the product does not declare coconut as an ingredient or allergen.

    Product
    MONAKA BELGIUM CHOCO & KURUMI DAIICHI F, 2.68 oz. (76 g), Plastic wrapping Keep Frozen Product of Japan distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA 90670 UPC 0 74410 71769 8
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1465-2019·2019-06-26

    Macy's Chocolate Pecan Clusters Recalled for Undeclared Allergens

    Gertrude Hawk Brands is recalling R.H. Macy & Co. Milk Chocolate Covered Pecan Caramel Clusters because the packaging failed to disclose the presence of almonds and pecans.

    Product
    R.H. Macy & Co. Milk Chocolate Covered Pecan Caramel Clusters, 7oz 1 unit per package, oval metal tin canister, 6 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1464-2019·2019-06-26

    Macy's Chocolate Pretzels Recalled for Undeclared Almond and Pecan Allergens

    Gertrude Hawk Chocolates is recalling R.H. Macy & Co. Milk Chocolate Covered Peanut Butter Pretzels because the packaging failed to list almonds and pecans.

    Product
    R.H. Macy & Co. Milk Chocolate Covered Peanut Butter Pretzels, 8 oz 1 unit per package, oval metal tin canister, 6 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1470-2019·2019-06-26

    Renaissance Food Group Recalls 365 Smoked Mozzarella Pasta Salad for Undeclared Soy

    Renaissance Food Group LLC is recalling 365 by Whole Foods Market Smoked Mozzarella Pasta Salad in Texas, Louisiana, and Oklahoma due to undeclared soy.

    Product
    365 by Whole Foods Market Smoked Mozzarella Pasta Salad packaged in a clear plastic clamshell 8 Oz. and a salad bar item UPC 81641602257
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1489-2019·2019-06-26

    Whole Foods Recalls Basil Pesto for Undeclared Allergens

    Whole Foods Market is recalling Basil Pesto sold in the Northeast because the labels failed to declare milk, walnuts, and pine nuts.

    Product
    Basil Pesto, sold by weight in plastic deli containers PLU code beginning with 255926
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1466-2019·2019-06-26

    R.H. Macy & Co. Dark Chocolate Sea Salt Caramels Recalled for Allergen Mislabeling

    Gertrude Hawk Brands is recalling R.H. Macy & Co. Dark Chocolate Sea Salt Caramels because the packaging failed to disclose the presence of almonds and pecans.

    Product
    R.H. Macy & Co. Dark Chocolate Sea Salt Caramels, 7 oz. 1 unit per package, oval metal tin canister, 6 units per case,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1467-2019·2019-06-26

    Gertrude Hawk Almond Toffee Recalled for Undeclared Allergens

    Gertrude Hawk Chocolates is recalling R.H. Macy & Co. Milk Chocolate Butter Almond Toffee because the packaging failed to disclose the presence of almonds and pecans.

    Product
    R.H. Macy & Co. Milk Chocolate Butter Almond Toffee, 6 oz. 1 unit per package, oval metal tin canister, 6 units per case,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1463-2019·2019-06-26

    Pearl Barley Recalled for Incorrect Gluten-Free Labeling

    Bedessee Imports is recalling National Heartland Naturals Pearl Barley because it was mistakenly labeled gluten-free despite containing gluten.

    Product
    National Heartland Naturals Premium Quality Pearl Barley 32 oz Plastic Bag, UPC 707966600083
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1471-2019·2019-06-26

    365 by Whole Foods Market Egg Salad Recalled for Undeclared Soy

    Renaissance Food Group LLC is recalling 365 by Whole Foods Market Traditional Egg Salad because it contains undeclared soy.

    Product
    365 by Whole Foods Market Traditional Egg Salad packaged in a clear plastic clamshell 9 Oz. UPC 81641602115
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1473-2019·2019-06-26

    Renaissance Food Group Recalls Veggie Crudite Bowls for Undeclared Soy

    Renaissance Food Group LLC is recalling 274 units of Veggie Crudite Bowls with Asparagus and Bell Peppers due to undeclared soy. The product was distributed in Texas, Louisiana, and Oklahoma.

    Product
    Veggie Crudite Bowl with Asparagus and Bell Peppers packaged in a Clear plastic bowl 34.5 Oz. UPC 82676681078
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1468-2019·2019-06-26

    Renaissance Food Group Recalls 365 Potato Salad for Undeclared Soy

    Renaissance Food Group LLC is recalling 365 by Whole Foods Market Classic Potato Salad due to undeclared soy. The product was sold in Texas, Louisiana, and Oklahoma.

    Product
    365 by Whole Foods Market Classic Potato Salad packaged in a clear plastic clamshell 8 Oz. and a salad bar item UPC 81641602117
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1806-2019·2019-06-26

    Arrow PICC Catheter Recalled for Incorrect Expiration Date Labeling

    Arrow International Inc. is recalling 162 units of Arrowg+ard Blue Advance PICC catheters due to an incorrect expiration date printed on the product.

    Product
    Arrowg+ard Blue Advance PICC pre loaded with Arrow¿ VPS" Precision Stylet Product Code: CDC 44052 VPS2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1791-2019·2019-06-26

    Arrow PICC Kit Recalled for Incorrect Expiration Date Labeling

    Arrow International Inc is recalling 1,840 units of Arrow PICC Kits because the product labels display an incorrect expiration date.

    Product
    Arrow PICC Kit Product Code: ASK 45552 RWJ4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1809-2019·2019-06-26

    Arrow International Recalls PICC Catheters Due to Incorrect Expiration Date

    Arrow International is recalling 350 units of Arrowg+ard Blue Advance PICC catheters because the product labels display an incorrect expiration date.

    Product
    Arrowg+ard Blue Advance PICC pre loaded with Arrow¿ VPS" Precision Stylet Product Code: CDC 45063 HPK1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1796-2019·2019-06-26

    Arrow PICC Catheters Recalled for Incorrect Expiration Date Labeling

    Arrow International is recalling 159 units of Arrow PICC catheters because the expiration date printed on the packaging is incorrect.

    Product
    Arrow PICC with Chlorag+ard Technology Product Code: CDA 45552 VPS2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1794-2019·2019-06-26

    Arrow PICC Catheters Recalled for Incorrect Expiration Date Labeling

    Arrow International Inc is recalling 185 units of Arrow PICC with Chloraguard Technology due to incorrect expiration dates on the packaging.

    Product
    Arrow PICC with Chlorag+ard Technology Product Code: CDA 45052 HPK1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1789-2019·2019-06-26

    Arrow PICC Kit Recalled for Incorrect Expiration Date Labeling

    Arrow International Inc is recalling 100 units of Arrow PICC Kits due to an incorrect expiration date printed on the product.

    Product
    Arrow PICC Kit Product Code: ASK 45541 RWJ4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1822-2019·2019-06-26

    Arrow PICC with Chloraguard Technology Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling Arrow PICC with Chloraguard Technology due to an incorrect expiration date on the product.

    Product
    Arrow¿ PICC with Chlorag+ard¿ Technology Product Code:PR 45552 HPHNM
    Category
    Medical Device
    Distribution
    Distributed nationwide