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.

5526–5550 of 9610

  • HighFDA (Food)·F-1510-2016·2016-06-22

    Clight Drink Mix Recalled for Undeclared Soy Ingredient

    Mondelez Puerto Rico is recalling Clight drink mix products because they contain soy lecithin but do not declare soy on the label.

    Product
    Label reads in part as: "Clight***Naranja*** Orange***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX***TWO PACKAGES IN ONE***MAKES 1 LITER***NET: 0.49 oz*** Distributed by: Mondelez Puerto Rico, LLC, Montehiedra Office Center Suite 801, 9615 Ave. Los Romeros, San Juan PR 00926-7037
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1513-2016·2016-06-22

    Clight Drink Mix Recalled for Undeclared Soy Ingredient

    Mondelez Puerto Rico is recalling Clight drink mix products because they contain soy lecithin but do not declare soy on the label.

    Product
    Label reads in part as: "Clight***Lim¿n*** Lemon ***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX***TWO PACKAGES IN ONE***MAKES 1 LITER***NET: 0.49 oz*** Distributed by: Mondelez Puerto Rico, LLC, Montehiedra Office Center Suite 801, 9615 Ave. Los Romeros, San Juan PR 00926-7037**
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1522-2016·2016-06-22

    Harris Teeter Recalls Gourmet Cranberry Crunch Cookies Due to Undeclared Peanut

    Harris Teeter is recalling Gourmet Cranberry Crunch Cookies because they contain undeclared peanut protein. Consumers should stop eating the product and return it to the store.

    Product
    Gourmet Cranberry Crunch Cookies, UPC 0007203695600, 4 Ct (Pack 24/4 Ct)
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1511-2016·2016-06-22

    Clight Drink Mix Recalled for Undeclared Soy Ingredient

    Mondelez Puerto Rico is recalling Clight drink mix products in four flavors because they contain soy lecithin but do not declare soy on the label.

    Product
    Label reads in part as: "Clight***Mandarina*** Tangerine***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX***TWO PACKAGES IN ONE***MAKES 1 LITER***NET: 0.49 oz*** Distributed by: Mondelez Puerto Rico, LLC, Montehiedra Office Center Suite 801, 9615 Ave. Los Romeros, San Juan PR 00926
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1996-2016·2016-06-22

    Ethicon Recalls EVARREST Fibrin Sealant Patch Due to Labeling Error

    Ethicon is recalling 228 units of EVARREST Fibrin Sealant Patch because the expiration date field on the foil pouch labels contains the text '0-bad' instead of the valid date.

    Product
    EVARREST Fibrin Sealant Patch, Manufactured by: Omrix Biopharmaceuticals, Ltd, Israel. Indicated for use with manual compression as an adjunct to hemostasis for control of bleeding during adult liver surgery and soft tissue bleeding in adults when control of bleeding by standa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1032-2016·2016-06-22

    Valeant Recalls Mislabelled Lodrane D Capsules Due to Incorrect Ingredient Labeling

    Valeant Pharmaceuticals is recalling 3,827 bottles of Lodrane D capsules because the outer cartons were mislabeled with the wrong active ingredient.

    Product
    Lodrane D (Brompheniramine maleate 4 mg and Pseudoephedrine HCl 60 mg) Capsules, 60-count bottles, Distributed by: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807, UPC 0 00950 86006 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1965-2016·2016-06-22

    Integra Recalls TS Series Depth Gauges for Incorrect Markings

    Integra LifeSciences is recalling 71 TS Series Depth Gauges because some units exceed length specifications or have incorrect millimeter markings.

    Product
    TS Series Depth Gauge for Integra Ti6 Internal Fixation System 2.0/2.5mm Screws The FS2030 Depth Gauge is used by the physician to determine the correct screw length when implanting a 2.0 or 2.5mm TS Series screw for the Ti6 Internal Fixation System.
    Category
    Medical Device
    Distribution
    9 states
  • LowFDA (Devices)·Z-1949-2016·2016-06-22

    Synthes Recalls Six LCP Dia-Meta Volar Distal Radius Plates Due to Packaging Error

    Synthes (USA) Products LLC is recalling six LCP Dia-Meta Volar Distal Radius Plates because the preprinted outer boxes were incorrect, though the internal product labels are accurate.

    Product
    LCP Dia-Meta Volar Distal Radius Plate 15 H Shaft/LT-Sterile; Indicated for fractures, osteotomies, and non-unions of the radius and other small bones.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Drugs)·D-1031-2016·2016-06-22

    Galderma Recalls Doxycycline Capsules Due to Missing Lot and Expiration Dates

    Galderma Laboratories is recalling Doxycycline USP Capsules 40 mg because some bottles are missing lot numbers or expiration dates.

    Product
    Doxycycline, USP Capsules 40 mg, Packaged in 30 ct Bottles, Rx Only. Marketed by: Prasco Laboratories, Mason, OH 45040 USA, Manufactured by: Catalent Pharma Solutions, LLC, Winchester, Kentucky 40391. NDC: 66993-815-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1036-2016·2016-06-22

    Sandoz Recalls Lisinopril Tablets Due to Missing Package Insert

    Sandoz Inc is recalling 3,048 bottles of Lisinopril Tablets USP, 30 mg, because the package insert is incorrect or missing.

    Product
    Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-0630-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1029-2016·2016-06-22

    Genzyme Recalls Hectorol Injection Vials Due to Incorrect Barcode Labeling

    Genzyme is recalling 2,350 vials of Hectorol (doxercalciferol) injection because the vial labels contain an incorrect barcode. The affected product was distributed to Michigan, Pennsylvania, and New Jersey.

    Product
    Hectorol (doxercalciferol injection) 2 mcg/1mL, Rx only, Manufactured by: Genzyme Biosurgery Corporation 500 Kendall Street, Cambridge, MA 02142, NDC 58468-0126-1
    Category
    Drug
    Distribution
    3 states
  • HighNHTSA·16V449000·2016-06-21

    GM Recalls 2016 Chevrolet Equinox and GMC Terrain for Incorrect Tire Labels

    General Motors is recalling specific 2016 Chevrolet Equinox and GMC Terrain vehicles because their certification labels may display incorrect tire and rim size information.

    Product
    GMC — GMC, CHEVROLET TERRAIN, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0973-2016·2016-06-15

    Novacare Recalls Unapproved Dietary Supplements Containing Salicylic Acid

    Novacare, LLC is recalling Xcellerator dietary supplements because FDA sampling confirmed the presence of salicylic acid in products marketed without an approved NDA/ANDA.

    Product
    Xcellerator (product not labeled)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1417-2016·2016-06-15

    Werner Butter Toffee Peanuts Recalled for Undeclared Milk Allergen

    Werner Gourmet Meat Snacks, Inc. is recalling Werner Brand Butter Toffee Peanuts because the labels declared butter but failed to declare milk as an ingredient.

    Product
    Werner Brand Butter Toffee Peanuts, net wt. 2.25 oz, UPC 7 09972 80113 3 Werner Brand Butter Toffee Peanuts, net wt. 6 oz., UPC 7 09972 80027 3 The ingredients statement declared: Peanuts, Sugar, Butter, Salt. The label contains an advisory statement Allergen Informa
    Category
    Food
    Distribution
    19 states
  • HighFDA (Food)·F-1437-2016·2016-06-15

    Frozen Inc. Recalls German Chocolate Dessert Bar Cake for Missing Pecan Labeling

    Frozen Inc. is recalling 24 oz German Chocolate Dessert Bar Cakes because the product does not list pecans on the label.

    Product
    24 oz RM German Choc. Dessert Bar Cake. Net Wt: 24 oz, K Dairy, UPC 752716883308, Vollmer's Bakery - 4004 Grape Street - Denver, CO - 303-388-8393. Packaging: Plastic Container, 8 per case, Keep frozen, refrigerate after opening.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1418-2016·2016-06-15

    Werner Brand Sweet Hot Crunch Mix Recalled for Undeclared Milk Allergen

    Werner Gourmet Meat Snacks is recalling Sweet Hot Crunch Mix because the label declares butter but fails to declare milk, a major allergen.

    Product
    Werner Brand Sweet Hot Crunch Mix, net wt. 2 oz, UPC 7 09972 80120 1. Werner Brand Sweet Hot Crunch Mix, net wt. 6 oz, UPC 7 09972 80100 3. The ingredients statement declared: "***BUTTER TOFFEE PEANUTS (PEANUTS, SUGAR, BUTTER, SALT)***". The label contains an
    Category
    Food
    Distribution
    19 states
  • HighFDA (Food)·F-1423-2016·2016-06-15

    Karlsburger Mesquite Seasoning Mix Recalled for Undeclared Soy Allergen

    Karlsburger Foods is recalling 2 lb containers of Mesquite Seasoning Mix because they contain undeclared soy, a major food allergen.

    Product
    Karlsburger, Mesquite Seasoning Mix & Marinade, Item 46402, Net WT 2 lbs in plastic shaker jars.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-1436-2016·2016-06-15

    Honest Kids Super Fruit Punch Recalled for Missing Apple Juice Labeling

    The Coca-Cola Company is recalling Honest Kids Super Fruit Punch because the label fails to list apple juice, a common allergen, as an ingredient.

    Product
    Honest Kids-Super Fruit Punch, Organic Juice Drink, 59 fluid oz. bottle, 006 57622 41273 7, Honest Tea, Inc., 4827 Bethesda Ave., Bethesda, MD 20814.
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-1942-2016·2016-06-15

    DePuy Synthes Recalls Norian Drillable Inject Due to Labeling Error

    DePuy Synthes is voluntarily recalling Norian Drillable Inject 3 CC-Sterile because the internal pouch may be labeled with the incorrect powder volume, though the actual contents are correct.

    Product
    Norian Drillable Inject 3 CC-Sterile; catalog # 07.704.003S Intended for bony voids or defects of the extremities and pelvis that are not intrinsic to the stability of the bony structure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1943-2016·2016-06-15

    DePuy Synthes Recalls Norian Drillable Inject Due to Labeling Error

    DePuy Synthes is voluntarily recalling Norian Drillable Inject 5 CC-Sterile units because the internal rotary pouch may be labeled with the incorrect powder volume, though the actual contents are correct.

    Product
    Norian Drillable Inject 5 CC-Sterile; catalog # 07.704.005S Intended for bony voids or defects of the extremities and pelvis that are not instrinsic to the stability of the bony structure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1919-2016·2016-06-15

    Synthes Rapid Resorbable Orbital Floor Plate Recalled for Labeling Errors

    Synthes (USA) Products LLC is recalling 19 units of 1.5 mm Rapid Resorbable Orbital Floor Plates due to potential expiration date discrepancies on outer packaging labels.

    Product
    1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate with Bending Template. Intended for use in fracture repair and reconstructive procedures of the craniofacial skeleton in pediatr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0977-2016·2016-06-15

    Bayer Recalls Coppertone Sunscreen Lotion for Undeclared Oxybenzone

    Bayer Health Care LLC is recalling 37,512 bottles of Coppertone Sunscreen Lotion, Clearly Sheer, Broad Spectrum SPF 50, because the product contains undeclared Oxybenzone.

    Product
    Coppertone SUNSCREEN LOTION, CLEARLY SHEER, BROAD SPECTRUM SPF 50, 5 FL OZ (147mL), OTC, Dist by: Bayer HealthCare LLC, Whippany, NJ 07981 --- NDC 11523-7391-1, UPC 00041100005762
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0976-2016·2016-06-15

    Pharmedium Recalls Potassium Chloride Injection Bags Due to Labeling Error

    Pharmedium Services is recalling 240 bags of Potassium Chloride Injection due to a labeling error where Potassium Phosphate was printed on the label stock.

    Product
    Potassium CHLORide added to 5% Dextrose Injection, 20 mEq 250 mL Bag, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 38141, NDC 61553-836-11, Service Code 2K5836.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1935-2016·2016-06-15

    Datascope Recalls Intra-Aortic Balloon Catheters Due to Incorrect Instruction Manual

    Datascope is recalling Mega and Sensation Plus Intra-Aortic Balloon Catheter kits because they were packaged with the wrong instruction manual for the STATLOCK device.

    Product
    MEGA¿ 7.5Fr. 30cc Intra-Aortic Balloon Catheter with Insertion Kit & STATLOCK¿ MEGA¿ 7.5Fr. 40cc Intra-Aortic Balloon Catheter with Insertion Kit & STATLOCK¿ MEGA¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit & STATLOCK¿ MEGA¿ 8Fr. 50cc Intra-Aortic Ballo
    Category
    Medical Device
    Distribution
    0 states