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.

Which agencies issued them

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.

4201–4225 of 9607

  • HighFDA (Food)·F-0002-2018·2017-10-11

    Country Harvest Black Thunder Bean Soup Recalled for Undeclared Milk

    Country Harvest is recalling Black Thunder Bean Soup because the label lists dairy whey but fails to declare milk, a major allergen.

    Product
    Country Harvest brand Black Thunder Bean Soup, dried soup mix is packaged in poly pro bag, heat sealed and placed in another poly pro bag & tape sealed. Net. 8 oz. UPC 7 29818 00104 6. The label is read in parts" ***For That Home Cooked Goodness***Country HARVEST ***BLACK THUN
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0010-2018·2017-10-11

    Good Eggs SF Recalls Panang Curry for Undeclared Peanut Allergen

    Good Eggs SF is recalling Panang Curry containers because peanuts are an ingredient but not listed as an allergen.

    Product
    Panang Curry included in the Beef Panang Curry Dinner, 3.5 oz. 8oz plastic deli container bearing the name Curry Paste. Ingredients: Shallots, Ginger, Garlic, Peanuts, Sugar, Tomato Paste, Fish Sauce(Anchovies, water, salt), Serrano Chili, Tumeric, Galangal, Lemon grass Cumin
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0001-2018·2017-10-11

    KIND Dark Chocolate Nuts and Sea Salt Bars Recalled for Undeclared Walnuts

    KIND LLC is recalling Dark Chocolate Nuts and Sea Salt Bars because the outer box fails to declare the allergen walnuts, although individual bars are properly labeled.

    Product
    KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.4 oz (40 g) bars Box :16.08 oz (480 g) per pack. Box UPC: 02652 17751
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3611-2017·2017-10-11

    Coborn's Caraway Rye Bread Recalled for Allergen Mislabeling

    Coborn's, Inc. is recalling 121 loaves of Caraway Rye Bread because the allergen statement was updated to include milk, egg, and soy, which were previously omitted.

    Product
    Coborn's/Cash Wise Caraway Rye Bread - UPC 7-33147-20155-8 Net Wt. 16 oz (1.0 lb) (454 g) Sell by 9/6/2017
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0001-2018·2017-10-11

    Carl Zeiss INTRABEAM PRS 500 Radiation Therapy Devices Recalled for Calibration Error

    Carl Zeiss Meditec AG is recalling nine INTRABEAM PRS 500 radiation therapy devices because they had incorrect printed calibration values on their certificates.

    Product
    Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABEAM System is indicated for radiation therapy treatments
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0007-2018·2017-10-11

    Implant Direct Recalls Swish Duo-Grip Healing Collars Due to Wrong Component

    Implant Direct is recalling 50 units of Swish Duo-Grip Healing Collars because the packages contained the wrong component size.

    Product
    Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3240-2017·2017-10-11

    Metrix Secure 100mL Vinyl Containers Recalled for Incorrect Material Labeling

    The Metrix Company is recalling Secure 100mL empty vinyl containers because the hot stamp label incorrectly states the material. The bags are correctly made of PVC.

    Product
    SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40), REF 58719, STERILE R,
    Category
    Medical Device
    Distribution
    4 states
  • HighNHTSA·17V634000·2017-10-09

    Thor Motor Coach Recalls 2017-2018 Motorhomes for Incorrect Cargo Labels

    Thor Motor Coach is recalling 2017-2018 motorhomes because incorrect water capacity labels may lead to vehicle overloading and increased crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR, THOR MOTOR WINDSPORT, VENETIAN, MIRAMAR, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·107-2017·2017-10-05

    Publix Homestyle Beef Pot Roast Recalled for Undeclared Wheat and Soybean Oil

    Sandridge RMH Acquisition, LLC is recalling 1,222 pounds of Publix homestyle beef pot roast because the product is mislabeled and contains undeclared wheat and soybean oil.

    Product
    Sandridge RMH Acquisition, LLC Recalls Ready-To-Eat Beef Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-3575-2017·2017-10-04

    Wegmans Dark Chocolate Cherry Cashew Granola Bars Recalled for Vitamin A

    Treehouse Foods is recalling Wegmans Dark Chocolate Cherry Cashew chewy granola bars because they may contain a higher concentration of Vitamin A than declared on the label.

    Product
    Wegmans Dark Chocolate Cherry Cashew chewy granola bars, 12-1.4OZ(40g) bars, Total Net Wt. 16.8OZ (1 LB 0.8OZ) 480g, UPC 77890-42230
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1178-2017·2017-10-04

    Teva Recalls Acarbose Tablets Due to Incorrect Expiration Date Labeling

    Teva Pharmaceuticals USA is recalling 3,275 bottles of Acarbose Tablets, 25 mg, because the product labeling displays an incorrect expiration date of July 2018 instead of the correct date of July 2017.

    Product
    Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; NDC 16252-523-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3212-2017·2017-10-04

    Teleflex Recalls LMA MADgic Devices Due to Labeling Deficiencies

    Teleflex Medical is recalling LMA MADgic devices because package labels may contain missing or incomplete information.

    Product
    LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 MADgic Intended for the application of topical anesthetics to the oropharynx and upper airway region
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3216-2017·2017-10-04

    Ultradent Paper Points Recalled Due to Sterile Barrier Labeling Error

    Ultradent Products, Inc. is recalling sterile Paper Points because the barcode label was placed underneath the sterile barrier and the product was re-wrapped.

    Product
    Ultradent Products, Inc. Paper Points, Size 30 PN #1555, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3214-2017·2017-10-04

    Ultradent Paper Points Recalled for Sterile Barrier Labeling Error

    Ultradent Products is recalling sterile Paper Points because the barcode label was placed underneath the sterile barrier, compromising the product's sterile status.

    Product
    Ultradent Products, Inc. Paper Points, Size 20 PN #1560, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3227-2017·2017-10-04

    Medtronic Heli-FX Guide Catheter Recalled for Labeling Mismatch

    Medtronic is recalling 20 units of the Heli-FX Guide 42 mm catheter because the deflection length on the handle does not match the box label.

    Product
    Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm, REF HG-18-90-42, STERILE EO, Rx Only The Heli-FX EndoAnchor System is intended to provide fixation and sealing between endovascular aortic grafts and the native artery. The Heli-FX System is indicated for
    Category
    Medical Device
    Distribution
    8 states
  • LowFDA (Drugs)·D-1179-2017·2017-10-04

    Sandoz Recalls Ampicillin Vials Due to Missing Labels

    Sandoz Inc is recalling 13,435 packs of Ampicillin for Injection because some vials are missing labels. The recall covers distribution in the USA and Puerto Rico.

    Product
    AMPICILLIN — AMPICILLIN (AMPICILLIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·105-2017·2017-10-03

    H-E-B Recalls Seasoned Diced Chicken Thighs for Undeclared Wheat Allergen

    H-E-B Meat Plant is recalling approximately 1,150 pounds of seasoned diced chicken thighs sold in Texas because the product contains wheat, an undeclared allergen.

    Product
    H-E-B Meat Plant Recalls Poultry Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • CriticalUSDA FSIS·103-2017·2017-09-29

    Belmont Sausage Recalls Smoked Turkey Drumsticks Due to Undeclared Milk Allergen

    Belmont Sausage Co. is recalling smoked turkey drumsticks because they contain undeclared milk, a known allergen. The products were distributed nationwide via an institutional location in Michigan.

    Product
    Belmont Sausage Co. Recalls Smoked Turkey Drumstick Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-3555-2017·2017-09-27

    Kelejete Dark Chocolate Energy Bar Recalled for Allergen Mislabeling

    Kelejete LLC is recalling Dark Chocolate Jete Nutritional Energy Bars because the label failed to declare peanuts and pecans in the 'Contains' statement.

    Product
    Dark Chocolate Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram. Product is package in a cellophane sealed wrapper. UPC 6 16320 77469 1. The label is read in parts: ***Dark Chocolate***Jete Nutritional Energy Bar***Contains Nuts***INGREDIENTS: Peanut Butter, A
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-3559-2017·2017-09-27

    Dierbergs Cabernet Grille Butter Recalled for Undeclared Wheat and Soy

    Dierbergs Markets is recalling Cabernet Grille Butter because it contains undeclared wheat and soy allergens.

    Product
    Cabernet Grille Butter, Net Wt. 3 OZ, packaged in clear plastic tubs. Dierbergs Kitchens
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-3571-2017·2017-09-27

    Laxmi Rusks Recalled for Undeclared Soy Allergen

    House of Spices India, Inc. is recalling Laxmi Rusks because the product may contain undeclared soy. Consumers with soy allergies should not eat the product.

    Product
    Laxmi Rusks, 10.58 OZ (300 gram) bags; UPC Code: 7 23246 26482 0
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-3544-2017·2017-09-27

    San Francisco Foods Seafood Salad Recalled for Undeclared Milk Allergen

    Simply Fresh Foods is recalling San Francisco Foods Seafood Salad with Greek Yogurt because the ingredient label may fail to declare milk as an allergen.

    Product
    San Francisco Foods Seafood Salad; Deli Style Seafood Salad with Greek Yogurt; 4 x 4 oz. (113 g) cups  Net Wt. 16 oz. (1 LB) 454 g; Carton UPC bar code of 47502 19701 Single Serve Cup: UPC 47502 19001 Perishable, Keep Refrigerated. Simply Fresh Foods, Inc. Buena Park
    Category
    Food
    Distribution
    6 states