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.

4226–4250 of 9607

  • HighUSDA FSIS·101-2017-EXP·2017-09-27

    Sausage Products Recalled for Undeclared Milk Allergen and Misbranding

    America New York RI Wang Food Group is recalling approximately 63,823 pounds of pork and beef sausage products due to misbranding and an undeclared milk allergen.

    Product
    America New York Ri Wang Food Group Co., Ltd. — America New York RI Wang Food Group Recalls Sausage Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3573-2017·2017-09-27

    NOW Foods Organic Coconut Sugar Recalled for Undeclared Gluten

    NOW Foods is recalling Organic Coconut Sugar because it contains undeclared gluten despite being labeled 'Gluten Free'.

    Product
    Organic Coconut Sugar, 16oz bag, 12 bags/case, packed in a foil bag
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3138-2017·2017-09-27

    Kamiya Biomedical Recalls K-Assay Multi-Analyte Calibrator Due to Incorrect Values

    Kamiya Biomedical is recalling specific lots of the K-Assay Multi-Analyte Calibrator because the Alpha-1 Antitrypsin (AlAT) values listed in the package insert were incorrect.

    Product
    K-Assay(R) Multi-Analyte Calibrator, REF KAI--016C, KAMIYA BIOMEDICAL COMPANY, Seattle, WA, IVD The K-ASSAY(R) Multi-Analyte Calibrator is intended to be used for the calibration of the K-ASSAY(R) Alpha-1 Acid Glycoprotein, Alpha-1 Anti-Trypsin, Complement C3, Complement C4, Hap
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Drugs)·D-1165-2017·2017-09-27

    PharMEDium Recalls Fentanyl Citrate Bags Due to Expired Diluent

    PharMEDium Services is recalling 590 bags of compounded Fentanyl Citrate because the diluent used was expired before the product's assigned expiration date.

    Product
    Fentanyl Citrate (Preservative Free) 10 mcg per mL (1,000 mcg per 100 mL) 100 mL total volume in a 100 mL LifeCare Bag in Sodium Chloride 0.9% Rx Only, Compounded by PharMEDium Services, LLC, Cleveland, MS 38732, NDC 61553-112-52.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1166-2017·2017-09-27

    PharMEDium Recalls Fentanyl Citrate Due to Expired Diluent

    PharMEDium Services is recalling 295 bags of compounded Fentanyl Citrate because the diluent used was expired before the product's assigned expiration date.

    Product
    Fentanyl Citrate (Preservative Free) 20 mcg per mL (2,000 mcg per 100 mL) 100 mL total volume in a 100 mL LifeCare Bag in Sodium Chloride 0.9% Rx Only, Compounded by PharMEDium Services, LLC, Cleveland, MS 38732, NDC 61553-605-52
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1174-2017·2017-09-27

    Medisca Recalls Aminocaproic Acid API Due to CGMP Labeling Deviations

    Medisca, Inc. is recalling Aminocaproic Acid API lots because the product was manufactured for industrial use but labeled for pharmacy compounding.

    Product
    Aminocaproic Acid, USP (6-Aminohexanoic Acid) active pharmaceutical ingredient, packaged in a) 100 g jar (NDC 38779-0989-05, b) 1 kg jar (NDC 38779-0989-09), and 25 kg drum (NDC 38779-0989-07), Rx only, Packed by Medisca Inc., Plattsburgh, NY 12901, CAS: 60-32-1. 38779-0989-05;
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3540-2017·2017-09-20

    Bateman Community Living Recalls Breaded Fish Meal Due to Allergen Mislabeling

    Bateman Community Living is recalling Breaded Fish with Vera Cruz Sauce because wheat and breading ingredients were not listed on the label.

    Product
    Breaded Fish with Vera Cruz Sauce; In 13.4 oz 3 compartment tray that has the fish, rice pilaf and green peas. Item number KD-0003 No labeling on individual trays, only on out box of 4 meals per case.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-3543-2017·2017-09-20

    Wegmans Assorted Muffins Recalled for Unlabeled Walnut Allergen

    Wegmans is recalling Assorted Muffins 4-Packs because they may contain walnuts that are not listed on the ingredient label.

    Product
    Wegmans Assorted Muffins 4-Pack-18 oz. (1 lb. 2 oz.) 510g packaged in clear plastic shell. UPC: 77890-22744 .
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-3542-2017·2017-09-20

    Zlotoklos Butter Cookies Recalled for Undeclared Milk Allergen

    Zlotoklos brand butter cookies are being recalled because the packaging lists butter but fails to identify milk as the source, violating FALCPA requirements.

    Product
    Zlotoklos brand Ciastka maslane w czekoladzie (Butter cookies in chocolate), 12.3 oz (350 g). Product is packaged in a plastic tray with foil overwrap, 12 packages per case.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1138-2017·2017-09-20

    Medline Recalls Mislabelled Vitamin A&D Ointment Packets

    Medline Industries is recalling Vitamin A&D Ointment packets that are incorrectly labeled as petroleum jelly. The outer boxes are correctly labeled.

    Product
    Vitamin A&D Ointment (petroleum 93.5%), Skin Protectant, NET Wt. 0.18 OZ (5g), Manufactured for Medline Industries, Inc., Northfield, IL 60093 USA. NDC: 53329-090-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1139-2017·2017-09-20

    VistaPharm Recalls Hydrocodone and Acetaminophen Oral Solution Due to Labeling Error

    VistaPharm, Inc. is recalling 3,084 bottles of Hydrocodone Bitartrate and Acetaminophen Oral Solution because the product was incorrectly labeled as a Class III controlled substance instead of a Class II controlled substance.

    Product
    Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL (Cherry Flavored), 473 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771 ---- NDC 66689-023-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·101-2017·2017-09-15

    Sausage Products Recalled for Undeclared Milk Allergen and Misbranding

    America New York RI Wang Food Group is recalling pork sausage products containing undeclared milk. The recall covers approximately 53,973 pounds distributed in New Jersey and New York.

    Product
    America New York RI Wang Food Group Recalls Sausage Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1133-2017·2017-09-13

    ImprimisRx Recalls Timolol Ophthalmic Drops Due to Undeclared Excipient

    ImprimisRx is recalling compounded Timolol ophthalmic drops because they were made with non-pharmaceutical grade PEG 40 Castor Oil due to supplier mislabeling.

    Product
    Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic Drops, Sterile 5ml Bottle, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1129-2017·2017-09-13

    Povidone Iodine Solution Recalled for Labeling Error

    Degasa Sa De Cv is recalling 720 bottles of Povidone Iodine 10% solution due to a label mix-up where 7.5% product was labeled as 10%.

    Product
    Povidone Iodine, USP Prep Solution, 10%, packaged in 1 gallon bottle, OTC, Manufactured for PSS World Medical, Inc. Southpoint Blvd. Jacksonville, FL Made in Mexico, NDC 68345-350-09
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-1131-2017·2017-09-13

    ImprimisRx Recalls Latanoprost Ophthalmic Drops Due to Undeclared Excipient

    ImprimisRx is recalling 19 bottles of compounded Latanoprost ophthalmic drops because they contain non-pharmaceutical grade PEG 40 Castor Oil due to supplier mislabeling.

    Product
    Latanoprost PF Solution, 0.005%, Ophthalmic Drops in Sterile 5ml Bottles, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1132-2017·2017-09-13

    ImprimisRx Recalls Timolol-Latanoprost Ophthalmic Drops Due to Mislabeling

    ImprimisRx is recalling 16 bottles of compounded Timolol-Latanoprost ophthalmic drops because non-pharmaceutical grade PEG 40 Castor Oil was used due to supplier mislabeling.

    Product
    Timolol-Latanoprost PF Solution (0.5-0.005)%, Ophthalmic Drops, Sterile 5ml Bottle, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V561000·2017-09-12

    Highland Ridge Recalls 2018 Open Range 3X Trailers for Tire Labeling

    Highland Ridge RV is recalling 2018 Open Range 3X fifth wheel trailers because tire size labels may be incorrect, potentially leading to the installation of wrong-sized tires.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW OPEN RANGE 3X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17T015000·2017-09-11

    Trek Tire Recalls Dunlop GrandTrek PT3A Tires for Missing DOT Markings

    Trek Tire is recalling specific Dunlop GrandTrek PT3A tires manufactured in December 2016 because they lack complete DOT identification markings, which may increase crash risk.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·100-2017·2017-09-08

    Northside Noodle Company Recalls Meatball Mix Due to Undeclared Soy Allergen

    Northside Noodle Company is recalling approximately 123 pounds of frozen meatball mix because the product contains soy, a known allergen, that is not declared on the label.

    Product
    Northside Noodle Co — Northside Noodle Company Recalls Meatball Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-3470-2017·2017-09-06

    Seven Sundays Muesli Recalled for Undeclared Almond Allergen

    Garden of Light Inc. is recalling Seven Sundays Vanilla Cherry Pecan Muesli because the product contains almonds but is labeled as containing only pecans.

    Product
    (a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch, UPC: 8-56088-00315-6 (b) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 2oz. cup UPC: 8-56088-00311-8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3469-2017·2017-09-06

    Gold Medal Caramel Corn Mix Recalled for Undeclared Soy

    Gold Medal Products Co is recalling Corn Treats Concentrated Caramel Corn Mix because the label is missing an ingredient statement and does not declare soy.

    Product
    CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-3480-2017·2017-09-06

    Schnucks Bakery German Chocolate Cakes Recalled for Unlabeled Pecans

    Schnucks Markets is recalling 13 German chocolate cakes mislabeled as Chocolate Iced Yellow Cake because they contain pecans not listed on the label.

    Product
    German chocolate cakes labeled as Schnucks Bakery Deluxe Petite Cake Chocolate Iced Yellow, Net Wt. 1 lb 1 oz (482 g), UPC 0 41218 31168 6
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-3468-2017·2017-09-06

    KIND Breakfast Dark Chocolate Cocoa Bars Recalled for Mislabeling

    KIND, LLC is recalling 4-count boxes of KIND Breakfast Dark Chocolate Cocoa Bars because the outer boxes may be mislabeled and contain KIND Breakfast PROTEIN Dark Chocolate Cocoa Bars.

    Product
    4-count boxes of KIND Breakfast Dark Chocolate Cocoa Bars 1.76 oz (50g) Outer Box: UPC: 60265220102-8
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3084-2017·2017-09-06

    Alere iScreen Dx Urine Drug Screen Card Recalled for Labeling Error

    Ameditech Inc is recalling Alere iScreen Dx Urine Drug Screen Cards because the kit box label incorrectly identifies PCP instead of TCA as a drug analyte.

    Product
    Alere iScreen Dx Urine Drug Screen Card, 20 Drug Detection, Kit Contents include 26 individually pouched devices and 1 IFU insert. The Alere iScreen Dx Drug Screen Card is a rapid urine screening test that can be performed without the use of an instrument. The test utilizes mon
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1111-2017·2017-08-30

    Phenobarbital Tablets Recalled Due to Incorrect Strength Labeling

    C. O. Truxton is recalling Phenobarbital 15 mg tablets that were actually 30 mg due to a labeling error.

    Product
    Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10
    Category
    Drug
    Distribution
    Distributed nationwide