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.

1576–1600 of 9607

  • HighFDA (Devices)·Z-1131-2021·2021-02-24

    Biomet Recalls Mislabelled 25mm Shoulder Prosthesis Central Screws

    Biomet is recalling 49 units of 25mm central screws for shoulder prostheses because they were mislabeled as 25mm but are actually 40mm.

    Product
    Central Screw 6.5x25mm - Product Usage: used as a sterile screw that is intended for implantable shoulder prosthesis assembly and/or fixation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1125-2021·2021-02-24

    Confirm Biosciences Recalls Healgen COVID-19 Rapid Test Cassettes

    Confirm Biosciences is recalling Healgen COVID-19 Rapid Test Cassettes because they were distributed to non-certified labs and not validated for fingerstick use.

    Product
    Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral flow immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV- 2 in human venous whole blood, plasma from antic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0257-2021·2021-02-24

    DLC Laboratories Recalls Sulfur Ointment Jars Due to Labeling Error

    DLC Laboratories is recalling 86,297 jars of Sulfur Ointment 10% because English labels for Camphor were incorrectly applied to the product.

    Product
    Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cruz Products, A Division of DLC Laboratories, Inc. Paramount, CA 9023 USA; UPC 024286150426
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0262-2021·2021-02-17

    Apotex Recalls Enoxaparin Syringes Due to Labeling Mixup

    Apotex Corp. is recalling Enoxaparin Sodium Injection syringes because some barrels may display incorrect concentration markings, posing a risk of dosing errors.

    Product
    Enoxaparin Sodium Injection, USP 120 mg/ 0.8 mL Single Dose Syringes with Automatic Safety Device For Subcutaneous Injection 10 x 0.8 mL Single Dose Syringes Rx Only,Manufactured by: Gland Pharma Ltd. Hyderabad, India Manufactured for: Apotex Corp. Weston, FL 33326 NDC 60505-079
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0261-2021·2021-02-17

    Apotex Recalls Enoxaparin Syringes Due to Labeling Mixup

    Apotex Corp. is recalling Enoxaparin Sodium Injection syringes because some barrels may display incorrect strength markings.

    Product
    Enoxaparin Sodium Injection, USP 100 mg/mL Single Dose Syringes with Automatic Safety Device For Subcutaneous Injection 10 x 1 mL Single Dose Syringes Rx Only, Manufactured by: Gland Pharma Ltd. Hyderabad, India Manufactured for: Apotex Corp. Weston, FL 33326 NDC 60505-0795-4 U
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0252-2021·2021-02-17

    Lidocaine/Tetracaine Ointment Recalled for Higher Concentration Than Listed

    Stanley Specialty Pharmacy is recalling Lidocaine/Tetracaine ointment because the lidocaine concentration is higher than listed on the label.

    Product
    Lidocaine/Tetracaine (LIPO110)* 23%/7% Ointment 100 GMS per 4 ounce plastic ointment jar, Rx Only, Stanley Specialty Pharmacy 3120 Latrobe Dr. Suite 200 Charlotte, NC 28211
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0954-2021·2021-02-17

    Becton Dickinson Recalls BioGX SARS-CoV-2 Reagents Due to Mislabeled Pouches

    Becton Dickinson is recalling 938 kits of BioGX SARS-CoV-2 Reagents because some master mix pouches may be mislabeled, potentially leading to false negative test results.

    Product
    BioGX SARS-CoV-2 Reagents for BD MAX System Catalog number (REF) 444213. In vitro diagnostic. SARS-CoV-2 Reagents is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal, nasal, mid-turbinate, and oropharyngea
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0288-2021·2021-02-17

    Bickel's Butter Flavored Popcorn Recalled for Undeclared Milk

    Bickel's Snack Foods Inc. is recalling 8-ounce bags of Butter Flavored Popcorn due to undeclared milk caused by mislabeling.

    Product
    Butter Flavored Popcorn Artificially Flavored 8oz. UPC:7017306021
    Category
    Food
    Distribution
    9 states
  • HighCPSC·21083·2021-02-17

    Anker Play Recalls Science Kits Due to Lead Paint Violation

    Anker Play Products is recalling 10-in-1 Incredible Inventions Science Kits because the red and blue magnet contains lead paint exceeding federal limits.

    Product
    10-in-1 Incredible Inventions Science Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1106-2021·2021-02-17

    Arrow AGB+ Multi-Lumen CVC Kit Recalled for Labeling Error

    Arrow International Inc. is recalling 1,705 kits due to a potential product code mislabeling that could cause delays or allergic reactions in sensitive patients.

    Product
    Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for venous access to the central circulation by the way of the femoral, jugular, or subclavian veins. Product Code: CDC-45703-1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0280-2021·2021-02-17

    Renaissance Food Group Recalls Buffalo Style Chicken Sliders Due to Labeling Error

    Renaissance Food Group, LLC is recalling Buffalo Style Chicken Sliders because the product label incorrectly lists ingredients for a different item and omits soy.

    Product
    BUFFALO STYLE CHICKEN Sliders NET WT. 5OZ (141g) Ingredients: Tuna Salad*** CONTAINS: EGG, FISH (TUNA), MILK, WHEAT Distributed By Renaissance Food Group, LLC 4322 Moreland Ave. Conley, GA 30288 UPC 8 26766 15590 3
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1099-2021·2021-02-17

    Cytocell Recalls Aquarius CRLF2 Distal Probe Due to Faint Signal Risk

    Cytocell Ltd. is recalling 72 units of the Aquarius LPH 511-A CRLF2 Distal Probe Green because faint additional signals may cause normal samples to be misreported as abnormal.

    Product
    Aquarius LPH 511-A CRLF2 Distal Probe Green, model no. LPH 511-A The CRLF2 Distal probe, labelled in green, consists of two probes (71kb and 131kb) that are situated distal (telomeric) to the CRLF2 gene
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Drugs)·D-0250-2021·2021-02-17

    Accord Recalls Glycopyrrolate Injection Due to Labeling Mix-up

    Accord Healthcare is recalling 502 cartons of Glycopyrrolate Injection due to a packaging error where 2 mL vials were placed in 1 mL blister strips.

    Product
    GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0273-2021·2021-02-10

    Wildtree Taco Seasoning Recalled for Undeclared Gluten

    Wildtree Inc. is recalling 593 units of Taco Seasoning because it contains undeclared gluten due to a contaminated ingredient.

    Product
    "Wildtree***Taco Seasoning***Organic & Gluten Free***Net Wt. 8 oz.***Distributed by: Wildtree"
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0274-2021·2021-02-10

    O Organics Plant Based Mushroom and Veggie Organic Burger Patties Recalled for Labeling Error

    Goodman Food Products Texas Inc is recalling O Organics Plant Based Mushroom and Veggie Organic Burger Patties because the packaging incorrectly claims the product is Gluten Free and Vegan, despite containing wheat and dairy.

    Product
    O Organics Plant Based Mushroom and Veggie Organic Burger Patties, 10 oz Package of 4/ 2.5oz patties packaged in cardboard box
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0952-2021·2021-02-10

    Topcon Harmony Referral System Recalled for Patient Data Mixing

    Topcon Medical Systems is recalling 13 Harmony Referral System units because software flaws allowed non-unique patient IDs to merge distinct patient records and images.

    Product
    Harmony Referral System (aka Harmony RS)/ Medical Device Data System - Product Usage: intended to be used by trained healthcare professionals and clinicians to access archived multimedia data, forms and patient information.
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Food)·F-0272-2021·2021-02-10

    Wildtree Leslie's Chili Blend Recalled for Undeclared Gluten

    Wildtree Inc. is recalling 273 units of Leslie's Chili Blend because the spice mix contains undeclared gluten due to a contaminated ingredient.

    Product
    "Wildtree***Leslies Chili Blend***Organic & Gluten Free***Net Wt. 3.7 oz. ***Distributed by: Wildtree"
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0942-2021·2021-02-10

    Fresenius Medical Care Recalls NaturaLyte Liquid Acid Concentrate Due to Missing Labels

    Fresenius Medical Care is recalling 2,280 cases of NaturaLyte Liquid Acid concentrate because bottles are missing product labels.

    Product
    Fresenius Medical Care NaturaLyte Liquid Acid concentrate-Liquid Acid Concentrate for Bicarbonate Hemodialyis Part Number: 08-3251-9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0934-2021·2021-02-10

    Brainreader Recalls Neuroreader Software Due to Database Discrepancy

    Brainreader ApS is recalling Neuroreader Medical Image Processing Software Version 2.4 because it was distributed with a reference database different from the FDA-cleared version.

    Product
    Neuroreader Medical Image Processing Software - Product Usage: intended to automate the current manual process of identifying, labeling, and quantifying the volume of segmentable brain structures identified on MR images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2113-2020·2021-02-03

    Stryker Recalls Mislabeled Intracardiac Ultrasound Catheters Due to Expiration Date Error

    Stryker is recalling 101 intracardiac ultrasound catheters labeled with incorrect expiration dates, posing risks of sterility breach or component breakdown.

    Product
    Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter, REF D087031, OM St. Jude Medical, Size 9F (3.2mm), Length 90 cm, Sterile EO, Rx Only, Quantity 1, UDI: 07613327376067
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Food)·F-0238-2021·2021-02-03

    Samyang Buldak Carbonara Sauce Recalled for Undeclared Allergens

    Samyang Foods is recalling Buldak Carbonara Hot Chicken Flavor Sauce because the label fails to declare egg and wheat.

    Product
    Samyang Buldak Carbonara Hot Chicken Flavor Sauce Hot Chili Sauce Net Wt. 200 g (7.05 oz) Product of Korea UPC: 8 801073 411432 Ingredients: Mixed milk powder (sugar, whole milk powder, butter powder, artificial flavor, red pepper powder, egg), Water, Corn syrup, Soy sauc
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0227-2021·2021-02-03

    Dole Chopped Kit Sesame Asian Salad Recalled for Undeclared Egg Allergen

    Dole Fresh Vegetables Inc is recalling specific lots of Chopped Kit Sesame Asian Salad due to an incorrect label that failed to declare egg as an ingredient.

    Product
    Dole Chopped Kit Sesame Asian Salad & Topping Net Wt: 9.5 oz (269 g) Dressing Net: 2.5 FL oz (72 mL) Total Net Wt. 12.25 oz (347 g) UPC 0-71430-00035-9
    Category
    Food
    Distribution
    9 states
  • HighNHTSA·21V048000·2021-02-03

    Yamaha Recalls Motorcycles and Scooters Due to Incorrect VIN Labels

    Yamaha is recalling 2019-2021 motorcycles and scooters because the VIN on the certification label may not match the vehicle, potentially preventing owners from receiving safety recalls.

    Product
    YAMAHA — YAMAHA YZF-R3, MT-03, CZD300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0923-2021·2021-02-03

    BD Stimex Insulated Needle Recall for Missing Contraindications

    Becton Dickinson is recalling BD Stimex Insulated Needles because the instructions for use lack general contraindications.

    Product
    BD Stimex Insulated Needle 22G x 2.13in ( 50 units/cs.) Indicated for administration of medications to affect anesthesia or analgesia to a specific anatomical location (region). Catalog No. 404204
    Category
    Medical Device
    Distribution
    18 states