The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 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 589 (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.

8651–8675 of 9611

  • HighFDA (Food)·F-1503-2013·2013-06-12

    Whey Protein Powder Recalled for Missing Milk Allergen Labeling

    Chemi-Source Inc. is recalling Delicious Whole-istic Whey Protein Duch Chocolate because the milk allergen was not listed on the label.

    Product
    Delicious Whole-istic Whey Protein Duch Chocolate 1.6 lbs: Whey Protein/Isolate, Contains: Dairy, Soy Lecithin UPC8-54809 0030-9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1476-2013·2013-06-12

    LL Bakery Recalls Bread and Danish for Undeclared Milk Allergen

    LL Bakery is recalling specific breads and pastries because the labels fail to declare milk as an allergen.

    Product
    Italian Cream Danish 8.5 oz (240g), 14pc/box. UPC 0 10314 40056 4. The pastry is braided and has yellow creamy swirls and sliced almonds. The label is white with black lettering and a tan colored border. The LL Bakery Logo is on the bottom left corner.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1495-2013·2013-06-12

    Metabolic Whey Protein Recalled for Undeclared Milk and Soy Allergens

    Chemi-Source Inc. is recalling Metabolic Whey protein products because milk and soy allergens were not properly labeled. Consumers with allergies to these ingredients should stop using the product.

    Product
    Metabolic Whey - Vanilla¿5 LBS French Vanilla 10lbs: Whey Protein/Isolate, Soy Lecithin UPC 6-09492 72051-1 (VANILLA) UPC 6-09492 72054-2 (FRENCH VANILLA)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1499-2013·2013-06-12

    Whey Protein Recall: Missing Milk Allergen Labeling

    Chemi-Source Inc is recalling All Natural Whey protein products because the milk allergen was not listed on the label.

    Product
    All Natural Whey - Rich Vanilla: 2.02 lbs, 1.01 lbs and 10pk/bx : Whey Protein/Isolate Contains: Soy, Dairy, Nitrozyme UPC 6-09492 72002-3 (2.02 lbs) UPC 6-09492 72006-1 (1.01 lbs) UPC 6-09492 72094-8 (10 pk)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1500-2013·2013-06-12

    Sprouts Farmers Market Whey Protein Vanilla Recalled for Undeclared Milk Allergen

    Sprouts Farmers Market Whey Protein Vanilla is being recalled because the whey ingredient is not listed as milk, a major allergen. Consumers with milk allergies are at risk of serious allergic reactions.

    Product
    Sprouts Farmers Market Whey Protein Vanilla: 1 lbs, 2 lbs : Whey Protein/Isolate, Soy Lecithin UPC 6-46670 68118-9 (1 lbs) UPC 6-46670 68124-0 (2 lbs)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1475-2013·2013-06-12

    LL Bakery Recalls Bread and Danish for Undeclared Milk Allergen

    LL Bakery is recalling specific bread and Danish products because the labels fail to declare milk as an allergen in the whey powder.

    Product
    Butter Farm Enriched White Bread 16 oz (454g), 9pc/box. UPC 0 10314 10004 4. The label is white with blue and green lettering and red design accents. The LL Bakery Logo is on the bottom left corner.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1483-2013·2013-06-12

    Chemi-Source Metabolic Whey Recalled for Undeclared Milk and Soy Allergens

    Chemi-Source Inc. is recalling Metabolic Whey protein powder because the packaging fails to list milk and soy as ingredients. Consumers with allergies to these substances are at risk of serious allergic reactions.

    Product
    UPC6-09492 72050-4, 72053-5 , Metabolic Whey - Rich Chocolate¿5 LBS, 10 LBS : Whey Protein Concentrate/ Isolate, Cocoa
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1479-2013·2013-06-12

    Whey Protein Powder Recalled for Undeclared Milk Allergen

    Chemi-Source Inc is recalling Isolate Whey Protein Chocolate Malt because the whey ingredient was not listed as milk, a major allergen.

    Product
    Isolate Whey Protein Chocolate Malt 2.03 LBS: Whey Protein Concentrate/ Isolate, Casein/Caseinate, Contains: Soy, Dairy, Cocoa, Xylitol ; UPC 6-09492 73010-7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1496-2013·2013-06-12

    Fruit-N-Whey Protein Powder Recalled for Unlabeled Milk Allergen

    Chemi-Source Inc is recalling Fruit-N-Whey protein powder because the whey ingredient was not listed as a milk allergen, posing a risk to consumers with milk allergies.

    Product
    Fruit-N-Whey 2.03lbs and Fruit-N-Whey Mixed Berries 2.03 lbs: Whey Protein/Isolate, Soy Lecithin. Contains: Dairy, Benefruit Blend, Natural Berry Flavors UPC 6-09492 72065-8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1497-2013·2013-06-12

    Flax-N-Whey Protein Recall for Undeclared Milk Allergen

    Chemi-Source Inc. is recalling Flax-N-Whey products because the whey ingredient contains milk, a major allergen, that is not listed on the label.

    Product
    Flax-N-Whey and Flax-N-Whey Vanilla Nut 1.99 lbs: Whey Protein/Isolate Contains: Soy, Dairy, Flaxseed UPC 6-09492 72064-1
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1487-2013·2013-06-12

    Chemi-Source Casein Powder Recalled for Unlabeled Milk Allergen

    Chemi-Source Inc. is recalling 1,320 units of 100% Micellar Casein powder because the milk ingredient was not listed as an allergen.

    Product
    Casein - 100% Micellar Casein - Cookies & Cream¿2.02 LBS: Soy Lecithin,Casein/Caseinate,Wheat UPC 6-09492 72242-3
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1486-2013·2013-06-12

    Coloplast Recalls Digitex Sutures Due to Incorrect Expiration Date Labeling

    Coloplast is recalling three lots of Digitex Absorbable Polydiaxanone Sutures because they are mislabeled with a three-year expiration date.

    Product
    Digitex Absorbable Polydiaxanone Suture, Size 2-0. Catalog Number / Code of product: 52031, 5203101400. The Digitex Delivery Device is a sterile, disposable device intended to deliver a suture to the operative site. The device assists in suturing by passing a needle through
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1465-2013·2013-06-12

    Biomet Recalls Active Articulation E1 Hip Bearing Implants Due to Labeling Errors

    Biomet is recalling 8 units of Active Articulation E1 hip bearing implants because outer and inner labels display incorrect or conflicting outer diameter sizes.

    Product
    Active Articulation E1. Intended for use with either primary or revision hip arthroplasty.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1517-2013·2013-06-12

    Invatec Diver C.E. Aspiration Catheters Recalled for Labeling Issues

    Invatec Llc is recalling 177 Diver C.E. aspiration catheters because the labeled indications for use were not included in the existing regulatory clearance.

    Product
    lnvatec SpA brand Diver C.E., Model/Catalog Numbers: DVR010014145, DVR011014145, Product is manufactured by lnvatec SpA, Roncadelle, Italy, and distributed by Invatec, Inc., Bethlehem, PA and by Medtronic Endovascular Therapies, Santa Rosa, CA The Diver C.E. product is an a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1441-2013·2013-06-12

    Optovue iVue Software Recall Due to Inconsistent Color Display

    Optovue, Inc. is recalling iVue software versions 3.0 and 3.1 because color displays for Ganglion Cell Complex thickness are inconsistent across different report types.

    Product
    Optovue iVue with Normative Database (NDB) with Software Version 3.0 and 3.1. Intended for in vivo imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1479-2013·2013-06-12

    Bion Enterprises IgG FITC Conjugate Recalled for Incorrect Expiration Date

    Bion Enterprises is recalling 504 units of IgG FITC Conjugate because the labeled expiration date is one year too long.

    Product
    Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Usage: Product is a used as a counterstain for various indirect fluorescent assay kits
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1478-2013·2013-06-12

    Bion Enterprises IgM Conjugate Recalled for Incorrect Expiration Date Labeling

    Bion Enterprises is recalling 201 units of IgM Conjugate because the labeled expiration date is one year too long.

    Product
    Plastic bottle containing 10.5 mL of IgM Conjugate Product Usage: Product is a used as a counterstain for various indirect fluorescent assay kits
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-596-2013·2013-06-12

    Voltaren 1% Gel Recalled for Illegible Lot and Expiration Dates

    Physicians Total Care is recalling 76 tubes of Voltaren 1% Gel because the lot number and expiration date on the tubes may not be legible.

    Product
    Voltaren 1% Gel, 100 gm tube, Rx only, Dist By: Physicians Total Care, Tulsa OK 74146, Mfg By: Novartis Consumer Health, Parsippany, NJ 07054, NDC 54868-5965-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-574-2013·2013-06-12

    Novartis Recalls Target Up & Up Athlete's Foot Cream for Labeling Issues

    Novartis is recalling Target Up & Up athlete's foot cream because the lot and expiration dates on the tubes may not be legible.

    Product
    Target Up & Up, athlete's foot cream, full prescription strength, terbinafine hydrochloride 1% antifungal, 30 g (1 oz), compare to active ingredient in Lamisil, NDC 0067-6382-30 & UPC code: 300676382302 (Novartis) Target NDC 1167-3401-04, Distributed by Target Corp., Minneapolis,
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-577-2013·2013-06-12

    Novartis Recalls Voltaren Gel Due to Illegible Lot and Expiration Dates

    Novartis Consumer Health is recalling Voltaren Gel because lot and expiration dates on the tubes may be illegible. The FDA classifies this as a Class III recall.

    Product
    Voltaren Gel (diclofenac sodium topical gel) 1%, for topical use only, RX only, a) Packaged in 20 gm tubes, NDC 63481-684-83 (physician sample product) and b) 100 gm tubes, NDC 63481-684-47 (the 100 g tubes are also packaged 3/100-g tubes/packs (UPC code: 363481684030 NDC code: 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1477-2013·2013-06-12

    Bion Enterprises IgG Conjugate Recalled for Incorrect Expiration Date Labeling

    Bion Enterprises Ltd is recalling 207 units of IgG Conjugate because the labeled expiration date is one year too long.

    Product
    Plastic bottle containing 10.5 mL of IgG Conjugate Product Usage: Product is a used as a counterstain for various indirect fluorescent assay kits
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-575-2013·2013-06-12

    Novartis Lamisil AT Cream Recalled for Illegible Lot and Expiration Dates

    Novartis is recalling 219,600 tubes of Lamisil AT Cream because the lot and expiration dates may be illegible.

    Product
    Novartis Lamisil AT Cream for Jock Itch (terbinafine hydrochloride 1% antifungal), a) 12 g (.42 oz) Tube, NDC 0067-3999-12, Novartis Consumer Health, Inc., Parsitan, NJ. UPC code: 300673999121, (Vertical Pack) and b) packaged in a horizontal package12 gm (.42 oz) Tube, NDC 00
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-576-2013·2013-06-12

    Novartis Recalls Lamisil AT Cream Due to Illegible Labeling

    Novartis Consumer Health is recalling specific lots of Lamisil AT Cream because the lot and expiration dates on the tubes may be illegible.

    Product
    Lamisil AT Cream (terbinafine hydrochloride 1% antifungal), 12 gm ( .42 oz) Tubes and 30 gm (1 oz) Tubes packaged in one box, Novartis Consumer Health, Inc., Parsitan, NJ. UPC code: 300676249438. (Club Pack), NDC 0067-6295-43
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-573-2013·2013-06-12

    Novartis Lamisil AT Cream Recalled for Illegible Lot and Expiration Dates

    Novartis is recalling Lamisil AT Cream because the lot and expiration dates on the tubes may be illegible. The recall covers 12-gm and 30-gm tubes distributed nationwide, in Puerto Rico, and in Panama.

    Product
    Novartis Lamisil AT Cream, Terbinafine Hydrochloride Cream 1% Antifungal, Novartis Consumer Health, Inc., Parsippany, NJ. (a)12 gm (.42 oz), packaged with UPC code 300673998421 and NDC code: 0067-3998-42; (b) 12 gm (.42 oz), packaged with UPC code: 300673998124 and NDC c
    Category
    Drug
    Distribution
    Distributed nationwide