The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (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.

5501–5525 of 9610

  • ModerateFDA (Devices)·Z-2086-2016·2016-07-06

    Integra LifeSciences Recalls Cadence Tibial Tray Implant Due to Labeling Error

    Integra LifeSciences is recalling 12 units of the Cadence Size 5 Left Tibial Tray Implant because the outer package label incorrectly identifies the material as Cobalt Chromium instead of Titanium.

    Product
    Cadence Size 5 Left Tibial Tray Implant, designed to treat ankle arthritis through replacement of the ankle joint with a prosthesis, thereby reducing pain, restoring alignment, and allowing for movement at the replaced joint. Catalog Number: 10207205; Lot Number #QJ0248
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2057-2016·2016-07-06

    Dynarex Recalls Specimen Containers Due to Incorrect Sterile Labeling

    Dynarex Corporation is recalling non-sterile specimen containers that were mistakenly packed in cartons labeled as sterile. The recall covers specific lots distributed in the US and Canada.

    Product
    dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal, Sterile, Single Use Only Product Usage:containers for sample collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2107-2016·2016-07-06

    Siemens Recalls SYNGO Breast Care Software Due to Display Issues

    Siemens is voluntarily recalling 29 units of SYNGO Breast Care software because patient information can obscure view markers and facility details are not shown by default.

    Product
    SYNGO Breast Care, visualization and image enhancement tools to aid radiologist in the review of digital Mammography images and tomosynthesis datasets.
    Category
    Medical Device
    Distribution
    12 states
  • LowFDA (Drugs)·D-1059-2016·2016-07-06

    Valeant Recalls Secobarbital Sodium Capsules Due to Missing Anaphylaxis Warning

    Valeant Pharmaceuticals is recalling 958 bottles of SECONAL SODIUM capsules because the package insert is missing a warning regarding anaphylaxis.

    Product
    SECONAL SODIUM (secobarbital sodium) Capsules, USP, 100 mg, 100 Ct. Bottles, Rx Only. Distributed by: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ 08807. NDC: 0187-4220-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2051-2016·2016-07-06

    Cardiovascular Systems Recalls ViperWire Advance Peripheral Guide Wire Due to Missing Date

    Cardiovascular Systems Inc is recalling ViperWire Advance Peripheral Guide Wire because the pouch label was missing the use-by date.

    Product
    ViperWire Advance Peripheral Guide Wire, Sterilized with Ethylene Oxide, Rx Only. Part number 72023-02, Model Number VPR-GW-17. Five (5) guide wire pouches in one (1) guide wire box. For use with CSI Peripheral Orbital Atherectomy Devices (OAD), including Stealth 360 and Diamond
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·054-2016·2016-07-01

    GHSE Recalls Chicken Salads Due To Undeclared Wheat Allergen

    GHSE, LLC is recalling approximately 5,682 pounds of ready-to-eat chicken salads because the packaging labels failed to declare wheat, a known allergen.

    Product
    GHSE, LLC — GHSE, LLC Recalls Chicken Products Due To Misbranding And Undeclared Allergen
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1560-2016·2016-06-29

    Let's Talk Health Energizer Drink Mix Recalled for Undeclared Milk

    Let's Talk Health, Inc. is recalling specific lots of Pomegranate Energizer Drink Mix due to undeclared whey protein, which contains milk and soy lecithin.

    Product
    Let's Talk Health Energizer Drink Mix Pomegranate 0.3oz UPC #91131180525
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·F-1536-2016·2016-06-29

    Candy and Baked Goods Recalled for Undeclared Milk and Soy Allergens

    The Caramel Factory, LLC. is recalling sugar free milk chocolate peanut clusters, candy, baked goods, and caramel icing due to undeclared milk and soy allergens.

    Product
    sugar free milk chocolate peanut cluster
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1557-2016·2016-06-29

    Golden Gourmet Veggie Chips Recalled for Undeclared Milk Allergen

    Bickel's Snack Foods is recalling Golden Gourmet Veggie Chips because ranch-flavored chips containing milk were packed in plain bags.

    Product
    Golden Gourmet Snacks Veggie Chips; Net Wt. 12 OZ; Bickel's Snack Foods, Inc., York, PA 17404 Lot codes: 26SEP16 Z4D1 and 26SEP16 Z5D1
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-1563-2016·2016-06-29

    Let's Talk Health Tox Elim Liquid Recalled for Undeclared Allergens

    Let's Talk Health is recalling 75 units of Tox Elim Liquid due to undeclared whey protein and soy lecithin, posing a risk to individuals with milk or soy allergies.

    Product
    Let's Talk Health Tox Elim Liquid 32oz. UPC #91131181119
    Category
    Food
    Distribution
    34 states
  • HighFDA (Food)·F-1526-2016·2016-06-29

    Sweet Earth Big Sur Breakfast Burrito Recalled for Undeclared Milk Allergen

    Sweet Earth Inc. is recalling Big Sur Breakfast Burritos because some units were packaged with Sana Cruz Burritos that contain milk, which is not declared on the Big Sur label.

    Product
    Big Sur Breakfast Burrito; A delicious blend of roasted potatoes & red peppers, smoked seitan and seasoned tofu. Net Wt. 7.0 oz. (198 g). Ingredients: Filling: Russet Potatoes, tofu (water, soybeans, Calcium sulfate, Calcium chloride, Sweet Earth Traditional Seitan (water,
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-2046-2016·2016-06-29

    Implant Direct Recalls InterActive Implant Open-Tray Transfers Due to Sizing Error

    Implant Direct is recalling 48 units of InterActive Implant Open-Tray Transfers because the wrong size was packaged, which may lead to oversized crown fabrication.

    Product
    6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number: 6534-08N Product Usage: Intended Use of Implant Direct Open Tray Transfers are to capture implant position in an elastomeric impression of the mandible or maxilla. Open Tray transfers stay within the Impre
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2048-2016·2016-06-29

    Medtronic Recalls Two EverFiex Stents Due to Outer Box Mislabeling

    Medtronic is recalling two Protege EverFiex Self-expanding Peripheral Stent Systems from lot A164580 because the outer box size label may not match the device inside.

    Product
    EV3 EverFiex" Self-expanding Peripheral Stent System, Sterilized using Ethylene Oxide, Rx Only, PRB35-08-040-080. The Protege EverFiex" Self-expanding Peripheral Stent System is a self-expanding Nitinol stent system intended for permanent implantation. The self-expanding stent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2038-2016·2016-06-29

    Cell Marque Recalls SIOOA I Rabbit Monoclonal Antibody Lots

    Cell Marque is recalling specific lots of SIOOA I Rabbit Monoclonal Antibody due to unacceptable IHC test results. The affected units were distributed in the US and several international countries.

    Product
    SIOOA I (EP I84) Rabbit Monoclonal Antibody; Catalogue numbers 408R-14, 408R-15, and 408R-16; Part number: 470361. Intended for identifying by light microscopy the presence of associated antigens in sections of formalin-fixed, paraffin embedded tissue sections using IHC test me
    Category
    Medical Device
    Distribution
    3 states
  • LowFDA (Drugs)·D-1049-2016·2016-06-29

    Prinston Recalls Irbesartan and Hydrochlorothiazide Tablets Due to Labeling Error

    Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because an incorrect lot number appears on the case label.

    Product
    IRBESARTAN AND HYDROCHLOROTHIAZIDE — IRBESARTAN AND HYDROCHLOROTHIAZIDE (IRBESARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·053-2016·2016-06-26

    Ghiringhelli Recalls Chicken Caesar Salad Due to Undeclared Allergens

    Ghiringhelli Specialty Foods is recalling approximately 2,444 pounds of Trader Giotto's Chicken Caesar Salad because the products contain undeclared soy, wheat, and fish, and are missing a shellfish warning.

    Product
    Ghiringhelli Brothers — Ghiringhelli Specialty Foods, Inc. Recalls Poultry Products Due To Mislabeling and Undeclared Allergens
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1487-2016·2016-06-22

    CSM Bakery Red Velvet Cake Recalled for Unlabeled Peanut Trace

    CSM Bakery Products is recalling 8-inch single-layer red velvet cakes because lab testing found trace amounts of peanuts, which were not declared on the label.

    Product
    8 " Single Layer Red Velvet Cake
    Category
    Food
    Distribution
    0 states