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.

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 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.

4901–4925 of 9607

  • ModerateFDA (Devices)·Z-1230-2017·2017-03-01

    Cardiovascular Systems Recalls Mislabelled Diamondback 360 Peripheral Atherectomy Components

    Cardiovascular Systems Inc is recalling 8 units of the Diamondback 360 Peripheral 1.50 Classic system because a 1.50mm Solid Crown OAD was mislabeled as a 1.50mm Crown OED.

    Product
    DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy System (OAS) is a minimally invasive, catheter-based OAS designed for improving luminal diameter in patients with peripheral arterial disease (PAD). PAD is caused by the accumulation of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1240-2017·2017-03-01

    Smith & Nephew Dyonics Saw Blade Recall for Missing Expiration Date

    Smith & Nephew is recalling Dyonics Saw Blades because they are provided sterile but lack an expiration date on the label.

    Product
    Smith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1231-2017·2017-03-01

    Quidel Recalls Influenza Transport Swab Packages Due to Incorrect Swabs

    Quidel Corporation is recalling Influenza Transport Swab Packages because they may contain incorrect sample swabs mixed with the proper ones.

    Product
    Influenza Transport Swab Packages, Reference #20171, One lot with 1010 packages (each package contains 25 transport tubes). The Influenza Swabs in dry transport tubes are intended for use with influenza tests
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1224-2017·2017-03-01

    Applied Medical Technology Recalls Expired Feeding Sets

    Applied Medical Technology is recalling 110 units of AMT 12-inch Right Angle Feeding Sets with Y-Ports due to expired expiration dates listed on the pouches.

    Product
    AMT 12 inch Right Angle Feeding Set with Y-Port Used with Nasogastric/Nasointestinal (NG/NI) tubes.
    Category
    Medical Device
    Distribution
    20 states
  • LowFDA (Drugs)·D-0489-2017·2017-03-01

    Sage Q Care Continue Care Kit Recalled for Incorrect Expiration Date

    Sage Products Inc is recalling 640 Q Care Continue Care Kits because the kit's printed expiration date is incorrect. The kits contain oral care products with an earlier expiration date than printed on the main kit.

    Product
    Q Care Continue Care Kit for the non-ventilated patient; kit contains 1 Covered Yankauer, 2 Suction Toothbrush packages with Corinz (cetylpyridinium chloride) Antiseptic Cleansing and Moisturizing Oral Rinse, and 2 Suction Oral Swab packages with Corinz (cetylpyridinium chloride)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1223-2017·2017-03-01

    Applied Medical Technology Recalls Nasal Tube Retaining Systems Due to Expired Dates

    Applied Medical Technology is recalling 110 units of the AMT Bridle Nasal Tube Retaining System because expired expiration dates are listed on the pouches.

    Product
    AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.
    Category
    Medical Device
    Distribution
    20 states
  • HighFDA (Food)·F-1472-2017·2017-02-22

    Whole Foods Key Lime Tarts Recalled for Undeclared Almond Flour

    Whole Foods Market is recalling specific Key Lime Tarts because they contain almond flour, a tree nut, which is not listed on the store scale label.

    Product
    Whole Foods Market, TART KEY LIME 4IN TART KEY LIME 4IN,TART KEY LIME 9IN
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1473-2017·2017-02-22

    Whole Foods Market Tart Chocolate Ganache Recalled for Allergen Mislabeling

    Whole Foods Market is recalling Tart Chocolate Ganache products because almond flour is missing from the scale label, posing a risk to consumers with nut allergies.

    Product
    Whole Foods Market, TART CHOCOLATE GANACHE SMALL, TART CHOCOLATE GANACHE LARGE
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1477-2017·2017-02-22

    Whole Foods Market Tart Lemon Small Recalled for Allergen Mislabeling

    Whole Foods Market is recalling Tart Lemon Small products because almond flour is not listed on the scale label, posing a risk to consumers with nut allergies.

    Product
    Whole Foods Market, TART LEMON SMALL
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1481-2017·2017-02-22

    BWI Inc Recalls Burt's British Potato Chips Due to Gluten Mislabeling

    BWI Inc is recalling Burt's British Hand Cooked Potato Chips because they are labeled gluten-free but contain gluten. The recall covers 653 cases distributed in 24 U.S. states and the Grand Cayman.

    Product
    Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-1470-2017·2017-02-22

    Whole Foods Tart Crusts Recalled for Unlabeled Almond Flour

    Whole Foods Market is recalling tart crusts because almond flour is missing from the scale label, posing a risk to people with nut allergies.

    Product
    Whole Foods Market, TART FRESH FRUIT AMERO SHELL LARGE
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1474-2017·2017-02-22

    Whole Foods Market Tarts Recalled for Missing Almond Allergen Labeling

    Whole Foods Market is recalling specific tart products because almond flour is not listed on the scale label, posing a risk to consumers with nut allergies.

    Product
    Whole Foods Market, SMALLTART FRESH BERRY SMALL, TART FRESH BERRY LARGE
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1221-2017·2017-02-22

    Atrium Medical Recalls 8 Fr Thoracic Catheters Due to Labeling Error

    Atrium Medical Corporation is recalling 8 Fr Straight Thoracic Catheters because the label depicts six eyelets instead of the correct two.

    Product
    Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1222-2017·2017-02-22

    Atrium Thoracic Catheter Recall Due to Incorrect Labeling Icon

    Atrium Medical Corporation is recalling 1,394 cases of 10 Fr Straight Thoracic Catheters because the label icon incorrectly depicts six eyelets instead of two.

    Product
    Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1484-2017·2017-02-22

    NOW Foods Recalls Multi-Food 1 Tablets Due to Labeling Error

    NOW Foods is recalling Multi-Food 1 Tablets because the label incorrectly states the molybdenum content is 75 mg instead of 75 mcg.

    Product
    NOW¿ Multi-Food 1 Tablets, One Tablet Daily, 90 tablets, A Dietary Supplement
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0477-2017·2017-02-22

    Taclonex Topical Suspension Recalled for Outdated Package Insert

    LEO Pharma Inc. is recalling Taclonex topical suspension because it was packaged with an out-of-date package insert.

    Product
    TACLONEX — TACLONEX (CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V106000·2017-02-17

    Keystone Recalls 2017 Dutchmen Coleman Trailers for Incorrect Tire Labeling

    Keystone is recalling 2017 Dutchmen Coleman recreational trailers because the Federal Identification Tag lists incorrect tire and rim sizes, which could lead to improper equipment use.

    Product
    DUTCHMEN — DUTCHMEN COLEMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1452-2017·2017-02-15

    Taylor Farms Rotini Pasta Salad Recalled for Undeclared Wheat Allergen

    Taylor Farms is recalling 10 oz. Rotini Pasta Salad containers because the label incorrectly identifies the product as mustard potato salad, failing to declare the wheat allergen.

    Product
    Fresh Foods Market Delicatessen Rotini Pasta Salad; Net Wt. 10 oz . (283g) Clamshell package. UPC Code: WO2017019 Perishable; Keep Refrigerated; Distributed by The Kroger Col., Cincinnati, OH
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1177-2017·2017-02-15

    Teleflex Recalls Sheridan Cuffed Tracheal Tubes Due to Labeling Inconsistency

    Teleflex Medical is recalling Sheridan cuffed tracheal tubes because some units are labeled with incorrect sizes, potentially leading to improper airway management.

    Product
    Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A tracheal tube is inserted into a patients mouth or nose for airway management
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Food)·F-1451-2017·2017-02-15

    Marich Chocolate Caramel Heart Recalled for Unlabeled Almond Allergen

    Marich Confectionery is recalling Chocolate Caramel Hearts because some boxes contained Triple Chocolate Toffee with almonds, which are not listed on the Caramel Heart label.

    Product
    MARICH Premium Chocolates; Chocolate Caramel Heart; Our delicious caramel hearts in rich milk and dark chocolate; Net Wt 4.25 oz. (120g) UPC 797817-44440-9
    Category
    Food
    Distribution
    3 states