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.

5026–5050 of 9610

  • ModerateFDA (Food)·F-1181-2017·2017-01-11

    Market Pantry Peanut Butter Cookies Recalled for Incorrect Labeling

    Minnesota Best Maid Cookie Co. is recalling Market Pantry Peanut Butter Cookies because the containers have an incorrect bottom label.

    Product
    Market Pantry Peanut Butter Cookies. Net Wt. 10.8 oz (306g) UPC 92180 11707
    Category
    Food
    Distribution
    3 states
  • ModerateNHTSA·17V008000·2017-01-09

    Heartland Recalls 2017 Mallard Trailers for Incorrect Certification Label

    Heartland is recalling 2017 Mallard recreational trailers because the certification label may contain incorrect tire size or pressure information, which could lead to improper tire inflation or overloading.

    Product
    HEARTLAND — HEARTLAND MALLARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·001-2017·2017-01-05

    4G Meat Processing Recalls Italian Sausage for Misbranding and Missing Labels

    4G Meat Processing LLC is recalling approximately 1,288 pounds of pork and turkey Caldarello Italian Sausage because the products contain undeclared MSG and lack required ingredients and safe handling statements on individual packages.

    Product
    4G Meat Processing LLC — Recall Notification Report 001-2017 (Italian Sausage)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1030-2017·2017-01-04

    Sunset Natural Products Recalls Aloe Vera Dietary Supplements Under Consent Decree

    Sunset Natural Products Inc. is recalling Aloe Vera dietary supplements pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2, 2014.

    Product
    Aloe Vera, 25 mg, Dietary Supplement (unknown container size)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0939-2017·2017-01-04

    Sunset Natural Products Recalls Magnun Plus Dietary Supplement

    Sunset Natural Products Inc. is recalling Magnun Plus dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.

    Product
    Magnun Plus, (30 per bottle)
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0940-2017·2017-01-04

    Starlight Creatives Recalls Star-Shaped Blue Frosted Tea Cookies for Undeclared Soy

    Starlight Creatives, Inc. is recalling star-shaped, blue frosted tea cookies sold in Massachusetts because they contain undeclared soy lecithin.

    Product
    Star shaped, blue frosted tea cookies. The cookies were delivered in plain white pastry boxes and sold unpackaged at the supermarket on the supermarkets Tea Cookie Display.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0934-2017·2017-01-04

    Sunset Natural Products Recalls Hepasil Dietary Supplement Capsules

    Sunset Natural Products Inc. is recalling 2,650,000 capsules of Hepasil pursuant to a consent decree requiring the destruction of supplements manufactured since April 2014.

    Product
    Hepasil, (various bulk amounts)
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0906-2017·2017-01-04

    Bio-Botanica Recalls Vitamin D-3 Drops for Excess Dosage

    Bio-Botanica is recalling Nature's Answer and Seeking Health Vitamin D-3 drops because the lots contain more Vitamin D3 than the label claims.

    Product
    Liquid VITAMIN D-3 Drops distributed under the following private labels and sizes: a) NATURE'S ANSWER VITAMIN D-3 DROPS DIETARY SUPPLEMENT, 0.5 FLUID OZ/15 mL, UPC 8300026132 -- Nature's Answer Hauppauge, NY 11788; and b) Seeking Health Optimal Vitamin D, Liquid Vitamin D-3 Drops
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0930-2017·2017-01-04

    Sterling Diagnostics Recalls HDL Cholesterol Kits Due to Expiration Date Error

    Sterling Diagnostics is recalling HDL Cholesterol diagnostic kits because previously extended expiration dates were rescinded.

    Product
    Sterling Diagnostics, Inc., HDL Cholesterol (PEF Method) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0903-2017·2017-01-04

    Ortho-Clinical Diagnostics Recalls VITROS Intact PTH Reagent Packs

    Ortho-Clinical Diagnostics is recalling VITROS Intact PTH Reagent Packs due to a positive bias of up to 20% and an incorrectly set reference interval.

    Product
    VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN 10758750006287 / Product Code 6802892 - Reagent Pack, 2) UPN 10758750006250 / Product Code 6802893 - Calibrators For the quantitative measurement of intact parathyroid hormone (iPTH) in human serum and plasma (E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0235-2017·2017-01-04

    Care-Tech Recalls Surgical Hand Scrub Due to Labeling and Cap Defects

    Care-Tech Laboratories is recalling Techni-Care Surgical Hand Scrub because bottles have missing or illegible lot and expiration dates, as well as defective or cracked caps.

    Product
    Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation (3.0% w/v Chloroxylenol), packaged in a) 4 oz. bottles (NDC 46706-201-01), b) 8 oz bottles (NDC 46706-201-02), c) 16 oz. bottles (NDC 46706-201-03), d) 12 oz. pumpette (NDC 46706-201-05), e) 32 oz. bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0931-2017·2017-01-04

    Sterling Diagnostics Recalls Creatinine Diagnostic Kits Due to Expiration Date Error

    Sterling Diagnostics is recalling 182 units of Creatinine/Endpoint diagnostic kits because previously extended expiration dates were rescinded.

    Product
    Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0934-2017·2017-01-04

    Sterling Diagnostics Recalls Colorimetric SGOT Kits Due to Expiration Date Error

    Sterling Diagnostics is recalling 165 Colorimetric SGOT diagnostic kits because previously extended expiration dates were rescinded.

    Product
    Sterling Diagnostics, Inc.Colorimetric SGOT for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0929-2017·2017-01-04

    Sterling Diagnostics Recalls Enzymatic Cholesterol Diagnostic Kits

    Sterling Diagnostics is recalling 97 units of Enzymatic Cholesterol diagnostic kits due to a revision of previously extended expiration dates.

    Product
    Enzymatic Cholesterol (Trinder/COD-CEH) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0932-2017·2017-01-04

    Sterling Diagnostics Recalls Enzymatic Glucose Diagnostic Kits

    Sterling Diagnostics is recalling 40 units of Enzymatic Glucose diagnostic kits due to a revision of previously extended expiration dates.

    Product
    Sterling Diagnostics, Inc., Enzymatic Glucose for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0936-2017·2017-01-04

    Sterling Diagnostics Recalls Urea Nitrogen Diagnostic Kits Due to Expiration Date Error

    Sterling Diagnostics is recalling 131 Urea Nitrogen diagnostic kits because previously extended expiration dates were rescinded. The kits were distributed in Michigan and the Philippines.

    Product
    Urea Nitrogen/Color BUN (Enzymatic Berthelot) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0935-2017·2017-01-04

    Sterling Diagnostics Recalls SGPT Colorimetric Kits Due to Expiration Date Error

    Sterling Diagnostics is recalling SGPT Colorimetric kits because previously extended expiration dates were rescinded.

    Product
    Sterling Diagnostics, Inc., SGPT Colorimetric for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0933-2017·2017-01-04

    Sterling Diagnostics Serum Iron/IBC Diagnostic Kits Recalled for Expiration Date Issues

    Sterling Diagnostics is recalling Serum Iron/IBC diagnostic kits because previously extended expiration dates were rescinded.

    Product
    Sterling Diagnostics, Inc. Serum Iron/IBC (Colorimetric) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0215-2017·2016-12-28

    Impax Recalls Lamotrigine Tablets Due to Labeling Mixup

    Impax Laboratories is recalling 3,074 boxes of Lamotrigine Orally Disintegrating Tablets because some 200 mg boxes contained 100 mg tablets.

    Product
    Lamotrigine Orally Disintegrating Tablets (ODT), 200 mg, 30 Tablets 3 blisters containing 10 tablets each, Rx only, Manufactured by: Watson Pharma Private Ltd., Verna, Salcette Goa INDIA, Distributed by: Impax Generics, Hayward, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0811-2017·2016-12-28

    Brownwood Farms Cherry BBQ Sauce Recalled for Undeclared Soy

    Brownwood Farms is recalling Cherry BBQ Sauce because it contains soy ingredients that are not declared on the label.

    Product
    Brownwood Farms Cherry BBQ Sauce. 21oz glass bottles, 1 gallon, 5 gallon. Private labels: Arbor Day Farm (Cherry BBQ Sauce). Bowers Harbor Vineyard (Cherry BBQ Sauce 12oz). Benjamin Twiggs (Northwoods Cherry BBQ Sauce 16oz). Crossroads. Friske Orchards. Kimmel Orchard &
    Category
    Food
    Distribution
    Distributed nationwide