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.

3226–3250 of 9607

  • HighFDA (Food)·F-0029-2019·2018-10-24

    Harris Teeter Frozen Yogurt Recalled for Unlabeled Peanut and Coconut Oil

    Harris Teeter is recalling Low Fat Frozen Yogurt (Cookies & Cream) because it contains peanuts and coconut oil not listed on the label.

    Product
    Harris Teeter Low Fat FROZEN YOGURT cookies & cream 1.5 QUART (1.42l) CONTAINS: MILK, WHEAT, SOY PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC MATTHEWS, NC 28105 UPC 0 72036 98182 0
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0037-2019·2018-10-24

    Lidl Recalls Bellona Chocolate Wafers Due to Missing Wheat Allergen Labeling

    Lidl US is voluntarily recalling Bellona brand chocolate wafers because the packaging fails to list wheat as an allergen.

    Product
    Bellona brand Milk Chocolate Flavored Coated Wafer with Hazelnut Cr¿me Filling and White Chocolate Flavor, 5.3 oz. (150g) package containing 7 single-serving, foil-wrapped chocolate wafers on a cardboard tray with foil overwrap.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0184-2019·2018-10-24

    OriGen Reinforced Dual Lumen Cannula Recalled for Manufacturing Deficiencies

    OriGen Biomedical is recalling 73 units of Reinforced Dual Lumen Cannulas due to missing barium sulfate and inaccurate tip length labeling.

    Product
    Reinforced Dual Lumen Cannula, 32Fr., REF: VV32F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support proced
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0109-2019·2018-10-24

    FDA Recalls Ambu Aura40 Reusable Laryngeal Masks Due to Labeling Error

    Besmed Health Business Corporation is recalling Ambu Aura40 Standard reusable laryngeal masks because they are packaged in pouches marked as single-use.

    Product
    Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0106-2019·2018-10-24

    Helena Laboratories Recalls Mislabeled Protein S ELISA Antigen Kits

    Helena Laboratories is recalling three Protein S ELISA Antigen Kits because internal components were mislabeled, causing the Substrate and Protein S Conjugate to be swapped.

    Product
    "Free and Total Protein S ELISA Kit" Cat. No. 5292 For use in the quantitation of free and total Protein antigen in citrated human plasma Contains: 96 Protein S: Ag Microwells, 3 x 0.5mL ELISA Reference Plasma, 1x12 mL Protein S Conjugate Solution, 1 x 60mL Sample Diluent, 1
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0104-2019·2018-10-24

    Valeris Medical Apollo Medial Suture Anchor Recalled for Mislabeling

    Valeris Medical is recalling 75 units of Apollo Medial Suture Anchors because the product was mislabeled as containing the incorrect type of suture.

    Product
    Valeris Medical Apollo Medial Suture Anchor, Catalog Number MSA-4515, 4.5 x 15mm, each package contains (1) PEEK Screw, (1) #2 ForceBraid Blue, and (1) #2 ForceBraid White, 5 packages per container, Sterile, Rx. The firm name on the label is Valeris Medical, Marietta, GA.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0121-2019·2018-10-24

    CryoLife Pulmonary Hemi-Artery Graft Recalled for Labeling Error

    CryoLife, Inc. is recalling one CryoPatch SG Pulmonary Hemi-Artery graft because the conduit and branch lengths were switched on the product labeling.

    Product
    CryoPatch SG Pulmonary Hemi-Artery, 1 graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0117-2019·2018-10-24

    Siemens Atellica IM CKMB Master Curve Material Recalled for Potential Bias

    Siemens Healthcare Diagnostics is recalling Atellica IM CKMB Master Curve Material due to a potential bias identified when compared to internal standards.

    Product
    Atellica IM CKMB Master Curve Material, Cat No. 10995534 Product Usage: For in vitro diagnostic use for evaluating the ADVIA Centaur CKMB assay. This material is intended to be run singly as unknown samples after a two-point calibration has been performed on the system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0180-2019·2018-10-24

    OriGen Biomedical Recalls Reinforced Dual Lumen Cannulas Due to Deficiencies

    OriGen Biomedical is recalling 452 units of Reinforced Dual Lumen Cannulas due to missing barium sulfate and incorrect tip length markings.

    Product
    Reinforced Dual Lumen Cannula, 16Fr., REF: VV16F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0025-2019·2018-10-24

    Mylan Recalls Levonorgestrel and Ethinyl Estradiol Tablets Due to Labeling Errors

    Mylan Pharmaceuticals is recalling specific lots of levonorgestrel and ethinyl estradiol tablets because the blister packs display incorrect NDC and product name information.

    Product
    Levonorgestrel and Ethinyl Estradiol Tablets, USP 0.15 mg/0.03 mg, Rx Only, 3 extended-cycle blister packs containing 91 tablets each, Made in India, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-7281-53.
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0015-2019·2018-10-17

    Magnesium Sulfate Injection Recalled Due to Mispackaged Heparin Unit

    Pfizer is recalling 94,752 bags of Magnesium Sulfate in Water for Injection because a single unit of Heparin was found inside a case.

    Product
    MAGNESIUM SULFATE IN WATER — MAGNESIUM SULFATE IN WATER (MAGNESIUM SULFATE IN WATER)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0025-2019·2018-10-17

    Sarap Asian Fusion Recalls Matcha Chocolate Cookies for Undeclared Allergens

    Sarap Asian Fusion is recalling Matcha Chocolate cookies because they contain undeclared wheat and soy lecithin. The cookies were sold online to customers in multiple states.

    Product
    Matcha Chocolate (cookies); A Sarap Asian Fusion Product; NET WT. 70 G/Cookie; Contains: Flour, eggs, Baking Soda, Baking Powder, Milk Powder, White Sugar, Brown Sugar, Salt, Butter, Matcha, Vanilla extract, milk chocolate. MFG at 12042 West St. Garden Grove, CA 92840
    Category
    Food
    Distribution
    44 states
  • ModerateFDA (Devices)·Z-0089-2019·2018-10-17

    Implant Direct Legacy Implant Closed-Tray Transfer Mislabeled Cap Recall

    Implant Direct is recalling 217 units of Legacy Implant Closed-Tray Transfer components due to potential cap mislabeling. The correct part number is on the main vial label.

    Product
    Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile, 3.5mmD Platform. Dental implant component, used temporarily during impressions for the prosthetic procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0021-2019·2018-10-17

    Hodgson Mill Gluten Free Cookie Mix Recalled for Ingredient Labeling Errors

    Hodgson Mill is recalling 707 cases of Gluten Free Cookie Mix because the packaging lists incorrect ingredients, omitting amaranth flour and baking soda while including baking powder and vanilla.

    Product
    Hodgson Mill Cookie Mix Gluten Free 12oz. cardboard carton retail unit; 6 retail units per case. UPC Code 0 71518 02125 2
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-0092-2019·2018-10-17

    Stryker Spine AVS Aria Cage Recalled for Incorrect Marker Placement

    Stryker Spine is recalling five AVS Aria Cage units because the anterior and posterior markers were placed on the incorrect sides of the device.

    Product
    AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral body fusion devices indicated for use with autogenous bone graft in patients with degenerative disc disease (DDD) at one level or two contiguous levels from L2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0016-2019·2018-10-17

    Xiromed Recalls Altavera Tablets Due to Generic Name Mislabeling

    Xiromed LLC is recalling Altavera tablets because the generic name on the packaging may cause confusion. The FDA classifies this as a Class III recall.

    Product
    ALTAVERA — ALTAVERA (LEVONORGESTREL AND ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowNHTSA·18V711000·2018-10-11

    Toyota Recalls 2018-2019 Tundra for Incorrect Load Capacity Label

    Toyota is recalling 2018-2019 Tundra vehicles because the load carrying capacity label incorrectly overstates weight by 10 pounds, failing federal safety standards.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1991-2018·2018-10-10

    Neighbors LLC Recalls Gluten-Free Cookie Dough for Undeclared Almonds

    Neighbors LLC is recalling 7,264 units of Crazy About Cookies Gluten Free Chocolate Chip Cookie Dough because the packaging fails to declare almonds as an ingredient.

    Product
    Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition facts***Ingredients: Whole grain sorghum flour, cane sugar, semi sweet chocolates**Contains eggs, milk and soy.***Manufactured in the same equipment that manufactures peanut, walnut
    Category
    Food
    Distribution
    40 states
  • HighFDA (Food)·F-0014-2019·2018-10-10

    Baker's Service Recalls Coconut & Cheese Pastry for Undeclared Wheat

    Baker's Service of South Florida, Inc. is recalling 28 cases of Coconut & Cheese Pastry because the finished product labeling failed to declare wheat.

    Product
    Coconut & Cheese Pastry. The product is packed in a cardboard box. The firm marks the Coconut& Cheese Pastry option printed on the box. Labeling on the cardboard box reads in part: WHOLESALE FROZEN BAKERY PRODUCTS, TRACY BAKERY,COCONUT & CHEESE PASTRY, HANDLING INSTRUCTIONS, P
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0012-2019·2018-10-10

    Baker's Service Recalls Coconut and Pineapple Pastry for Undeclared Wheat

    Baker's Service of South Florida, Inc. is recalling 58 cases of Coconut and Pineapple Pastry because the product labeling failed to declare wheat.

    Product
    Coconut and Pineapple Pastry. The product is packed in a cardboard box. The firm marks the Coconut and Pineapple Pastry option printed on the box. Labeling on the cardboard box reads in part: WHOLESALE FROZEN BAKERY PRODUCTS, TRACY BAKERY,COCONUT AND PINEAPPLE PASTRY, HANDLING
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0013-2019·2018-10-10

    Baker's Service Recalls Coconut Pastry for Undeclared Wheat

    Baker's Service of South Florida, Inc. is recalling 344 cases of Coconut Pastry because the finished product labeling failed to declare wheat.

    Product
    Coconut Pastry. The product is packed in a cardboard box. The firm marks the Coconut Pastry option printed on the box. Labeling on the cardboard box reads in part: WHOLESALE FROZEN BAKERY PRODUCTS, TRACY BAKERY,COCONUT PASTRY, HANDLING INSTRUCTIONS, PREPARATION & BAKING, INGRE
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0011-2019·2018-10-10

    Baker's Service Recalls Apple Pastry for Undeclared Wheat Allergen

    Baker's Service of South Florida, Inc. is recalling Apple Pastry because the labeling failed to declare wheat, a major food allergen.

    Product
    Apple Pastry. The product is packed in a cardboard box. The firm marks the Apple Pastry option printed on the box. Labeling on the cardboard box reads in part: WHOLESALE FROZEN BAKERY PRODUCTS, TRACY BAKERY, APPLE PASTRY, HANDLING INSTRUCTIONS, PREPARATION & BAKING, INGREDIENT
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-3280-2018·2018-10-10

    Ortho-Clinical VITROS Sodium Slides Recalled for Potential Positively Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Sodium Slides due to a potential for positively biased results. The recall covers multiple generations and expiry dates distributed globally.

    Product
    VITROS Sodium Slides, Catalog # 837 9034
    Category
    Medical Device
    Distribution
    Distributed nationwide