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.

2901–2925 of 9607

  • HighFDA (Food)·F-1284-2019·2019-04-03

    Surtidoras Bakery Recalls Blueberry Muffins Due to Undeclared Milk Allergen

    Surtidoras Bakery Inc is recalling 44 packages of Blueberry Muffins distributed in Washington because the product contains milk but does not list it on the label.

    Product
    Blueberry Muffin, brand Surtidoras Bakery, net wt. 1.74 lbs., packaged in rigid plastic clam shell container. No UPC. The allergens declared in the INGREDIENTS statement: "***ENRICHED WHEAT FLOUR *** SOYBEAN OIL***WHEY***WHEAT GLUTEN***EGGS*** SOY FLOUR***SOYBEAN OIL AND WHOLE
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1279-2019·2019-04-03

    Surtidoras Bakery Pecan Cookies Recalled for Peanut Oil Allergen Mislabeling

    Surtidoras Bakery is recalling 30 packages of Pecan Cookies because the ingredients list declares peanut oil, but the 'Contains' statement omits it.

    Product
    Pecan Cookies, brand Surtidoras Bakery, net wt. 1.08 lbs., packaged in rigid plastic clam shell container. No UPC. The allergens declared in the INGREDIENTS statement: "***UNBLEACHED WHEAT FLOUR *** MILK *** EGGS*** PECANS*** PEANUT OIL ***". The allergens declared in the C
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1277-2019·2019-04-03

    Surtidoras Bakery Recalls Kid's Chocolate Cookies for Undeclared Coconut Allergen

    Surtidoras Bakery is recalling 20 packages of Kid's Chocolate Cookies because the packaging fails to declare coconut in the 'Contains' statement, despite listing it in the ingredients.

    Product
    Kid's Chocolate Cookies, brand Surtidoras Bakery, net wt.15.52 oz., packaged in rigid plastic clam shell container. No UPC. The allergens declared in the INGREDIENTS statement: "***KIDS CHOCOLATE COOKIES***ENRICHED WHEAT FLOUR BLEACHED*** SOYBEAN OIL***MILK***SOY LECITHIN ***
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1186-2019·2019-04-03

    Klaire Labs Reduced L-Glutathione Recalled for Containing Lithium Orotate

    ProThera, Inc. is recalling Klaire Labs Reduced L-Glutathione capsules because they are mis-packaged and contain Lithium Orotate instead of the labeled ingredient.

    Product
    Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9
    Category
    Drug
    Distribution
    14 states
  • HighFDA (Food)·F-1285-2019·2019-04-03

    Surtidoras Bakery Mini-Puff Pastry Ears Recalled for Soy Allergen Mislabeling

    Surtidoras Bakery is recalling Mini-Puff Pastry Ears because the packaging fails to declare soy in the 'Contains' statement, despite listing soybean oil in the ingredients.

    Product
    Mini-Puff Pastry Ears, brand Surtidoras Bakery, net wt. 10.4 oz., packaged in rigid plastic clam shell container. No UPC. The allergens declared in the INGREDIENTS statement: "***ENRICHED WHEAT FLOUR *** SOYBEAN OIL***". The allergens declared in the CONTAINS statement: "CO
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1057-2019·2019-04-03

    Randox Blood Gas Control Level 2 Recalled for pH Range Error

    Randox Laboratories is recalling Blood Gas Control Level 2 kits due to an error in the assignment of the control range pH.

    Product
    Randox Blood Gas Control Level 2 -Model BG5002. In-vitro Diagnostic Quality control of Blood Gas analysis This product is intended for in vitro diagnostic use, in the quality control of Blood Gas analysis. Target values and ranges are supplied for the following analytes: Calc
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Food)·F-1188-2019·2019-04-03

    Jimmy's Original Blue Cheese Salad Dressing Recalled for Labeling Error

    Fish House Dressing is recalling 1,741 jars of Jimmy's Original Blue Cheese Salad Dressing because the product may be mislabeled as French Blue Cheese.

    Product
    Jimmy's Original Blue Cheese Salad Dressing 15 Fl. Oz (443 ml). UPC 86824-22345 Keep Refrigerated. Manufactured by: Fish House Dressing, 1171 2nd Ave NE, Stewartville, MN 55976
    Category
    Food
    Distribution
    3 states
  • LowFDA (Devices)·Z-1073-2019·2019-04-03

    CryoLife Recalls Two On-X Aortic Heart Valves for Mislabeled Serial Numbers

    CryoLife, Inc. is recalling two On-X Aortic Heart Valves because they were mislabeled with incorrect serial numbers. The devices were distributed in Georgia and Germany.

    Product
    On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: The On-X Prosthetic Heart Valve is indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valves in the aortic position. It is a bileaflet mechanical heart valve, which
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·039-2019·2019-03-30

    Market of Choice Recalls Pork and Poultry Pâté for Undeclared Allergens

    Market of Choice is recalling pork and poultry pâté products containing undeclared milk and soy allergens. No adverse reactions have been reported.

    Product
    Market of Choice, Inc. Recalls Pork and Poultry Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·19V241000·2019-03-27

    Volkswagen Recalls 2019 Tiguan LWB for Inaccurate Tire Information Label

    Volkswagen is recalling 2019 Tiguan LWB vehicles because the tire information label contains inaccurate dimension and pressure specifications, which may increase crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1180-2019·2019-03-27

    Best Choice Pancake Mix Recalled for Undeclared Milk Allergen

    Gilster-Mary Lee Corp. is recalling Best Choice Pancake & Waffle Complete Mix Original because the product contains milk but the packaging does not declare it as an ingredient.

    Product
    Best Choice Pancake & Waffle Complete Mix Original 32oz. retail carton, 12 retail units per wholesale case. UPC# 70038 30212
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·19V244000·2019-03-27

    Toyota Recalls 2019 Models Due to Illegible Load Capacity Labels

    Toyota is recalling specific 2019 models because the load capacity label text may become illegible, potentially leading to vehicle overload and increased crash risk.

    Product
    TOYOTA — TOYOTA CAMRY, AVALON, PRIUS, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1018-2019·2019-03-27

    Randox Fructosamine Control 3 Calibrator Recall Due to Value Reassignment

    Randox Laboratories is recalling 133 kits of Fructosamine Control 3 because the assigned value was decreased by 25%. The product is used for in vitro calibration.

    Product
    Fructosamine Control 3, FR2996 This product is intended for in vitro use in the calibration of the Randox Liquid Fructosamine assay on clinical chemistry systems.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1007-2019·2019-03-27

    Docusate Sodium Softgels Recalled Due to Incorrect Secondary Carton Labeling

    Rx Pak Division of McKesson Corporation is recalling Docusate Sodium 100mg softgels because secondary cartons may be mislabeled as Gabapentin 300mg.

    Product
    Docusate Sodium, 100mg softgels, packaged in 10 x 10 unit dose blister cards, For institutional use only, Mfg by: Aenova Holding GmBh, Miami, Fl 33186, NDC 63739-0478-10
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1028-2019·2019-03-27

    Smith & Nephew Recalls Mislabelled Hip Stem Implants Due to Size Error

    Smith & Nephew is recalling 58 hip stem implants because the outer label incorrectly identified the product as size "1" instead of "-1".

    Product
    smith&nephew SMF(TM) STANDARD OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1 SIZE, STEM, REF 713552510
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1016-2019·2019-03-27

    Randox Fructosamine Calibrator Recall Due to Value Reassignment

    Randox Laboratories is recalling 85 kits of Fructosamine Calibrator FR2993 because the assigned value was decreased by 25%.

    Product
    Fructosamine Calibrator, FR2993 This product is intended for in vitro use in the calibration of the Randox Liquid Fructosamine assay on clinical chemistry systems.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1029-2019·2019-03-27

    Smith & Nephew Recalls Mislabelled High Offset StikTite Coated Hip Stems

    Smith & Nephew is recalling 9 units of hip stems where the outer label incorrectly identified the product as size "1" instead of the actual size "-1".

    Product
    smith&nephew SMF(TM) HIGH OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1H SIZE, STEM, REF 713552511
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1017-2019·2019-03-27

    Randox Fructosamine Calibrator Recall Due to Value Reassignment

    Randox Laboratories is recalling 141 kits of Fructosamine Control 1 because the assigned value was decreased by 25%.

    Product
    Fructosamine Control 1, FR2994 This product is intended for in vitro use in the calibration of the Randox Liquid Fructosamine assay on clinical chemistry systems.
    Category
    Medical Device
    Distribution
    4 states
  • SevereUSDA FSIS·035-2019·2019-03-22

    Two Brothers Pork Skins Recalled for Misbranding and HACCP Failures

    Two Brothers Pork Skins is recalling pork skin products in North Carolina and South Carolina due to misbranding and failure to produce under a HACCP plan.

    Product
    Two Brothers Pork Skins — Two Brothers Pork Skins Recalls Pork Skin Products Due to Misbranding and Failure to Produce Under A HACCP Plan
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1155-2019·2019-03-20

    Perrigo Recalls Simple Truth Organic Fruit Puree Pouches for Milk Labeling Error

    Perrigo is voluntarily recalling Simple Truth Organic Fruit Puree pouches because the packaging fails to declare the presence of milk.

    Product
    Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate pouch, Each case has 6 cartons with 6 pouches per carton. Total of 36 pouches per case.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1006-2019·2019-03-20

    FDA Recalls NexGen Trabecular Metal Tibial Augments Due to Labeling Mismatch

    Zimmer Trabecular Metal Technology is recalling 26 units of NexGen Trabecular Metal Tibial Half Block Augments because the product in the box may not match the label.

    Product
    NexGenTrabecular Metal Tibial Half Block Augment, Left Lateral/Right Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800436 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the kne
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1156-2019·2019-03-20

    Finax Muesli Recalled for Unlabeled Hazelnut Allergen

    Chicago Importing Co is recalling Finax Muesli with Nuts and Fruit because the product was mislabeled and contains hazelnuts not listed on the label.

    Product
    Finax Muesli with Nuts and fruit 22.9-oz. Heat sealed plastic bag; 10 bags/case UPC: 7311142201402
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-1168-2019·2019-03-20

    Nature's Path Organic Gorilla Munch Corn Puffs Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Gorilla Munch Corn Puffs cereal because it may contain undeclared gluten (wheat and barley). The recall covers 23,969 cases distributed nationwide and internationally.

    Product
    Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g), UPC 58449-86002. Nature's Path Foods, Inc., Blaine, WA 98230.
    Category
    Food
    Distribution
    Distributed nationwide