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.

8751–8775 of 9611

  • HighFDA (Food)·F-1375-2013·2013-05-08

    Buffalo Trace Barbecue Sauce Recalled for Missing Soy and Anchovy Allergens

    Buffalo Trace Distillery is recalling 16 fl. oz. jars of Original Flavor Barbecue Sauce because the label failed to list soy and anchovy allergens.

    Product
    BUFFALO TRACE ORIGINAL FLAVOR BARBEQUE SAUCE Net Wt. 16 fl. oz./532 ml PRODUCED BY: APPLECREEK ORCHARDS LLC P.O. Box 8383 Lexington, KY 40533 BUFFALO TRACE DISTILLERY 113 Great Buffalo Trace Franklin County Frankfort, KY 40601 800-654-8471 e-mail: [email protected] web
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Food)·F-1355-2013·2013-05-08

    Vanilla Eskimo Dessert Bar Recalled for Undeclared Food Dye

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz Vanilla Eskimo Dessert Bars because the product contains undeclared FD&C Yellow #6.

    Product
    Vanilla Eskimo Dessert Bar , 4 oz. Undeclared FD&C Yellow # 6 in clear flexible package, ingredients: water, chocolate coating (coconut oil, sugar, partially hydrogenated coconut and soybean oil, cocoa, corn starch, soy lecithin, etc.) red 40, yellow 5 UPC Code 8 94163 00230 4
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1354-2013·2013-05-08

    Mango Dessert Bar Recalled for Undeclared Food Dyes

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Mango Dessert Bars because they contain undeclared FD&C Yellow # 6 and Blue # 1.

    Product
    Mango Dessert Bar, 4 oz. Undeclared FD&C Yellow # 6 and Blue # 1 in clear flexible plastic. Ingredients: water, sugar, mango, partially hydrogenated palm kernel oil, nonfat milk solids UPC Code 8 94163 00220 5
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-306-2013·2013-05-08

    Donnatal Extentabs Recalled for Incorrect Expiration Date Labeling

    West-ward Pharmaceutical is recalling 1,258 bottles of Donnatal Extentabs because the bottles are labeled with an expiration date of April 2015 instead of the correct April 2013.

    Product
    Donnatal Extentabs, 0.3888mg/46.8mg, 100-count bottle (NDC # 66213-421-10), Rx only Manufactured By: West-ward Pharmaceutical, 435 Industrial Way West, Eatontown, NJ 07724 Manufactured For: PBM Pharmaceuticals, Inc. Gordonsville, VA 22942.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1214-2013·2013-05-08

    NxStage PureFlow-B Solution Recalled for Potential Mislabeled Product

    NxStage Medical is recalling 1,480 cases of PureFlow-B Solution due to potential mislabeling. The product is used for hemodialysis.

    Product
    NxStage PureFlow-B Solution, Model/Catalog Number: RFP-401, packaged in a case The NxStage PureFLow-B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1359-2013·2013-05-08

    Watermelon Fruit Bar Recalled for Undeclared FD&C Blue # 1

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Watermelon Fruit Bars because they contain undeclared FD&C Blue # 1. The product was sold in Michigan and Indiana.

    Product
    Watermelon Fruit Bar , 4 oz. Undeclared FD&C Blue # 1 packaged in clear flexible plastic ingredients: water, watermelon, sugar, red 40 UPC Code 8 94163 00210 6
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1357-2013·2013-05-08

    Spicy Cucumber Fruit Bar Recalled for Undeclared Food Dyes

    Paleteria Y Neveria La Rosita, LLC is recalling Spicy Cucumber Fruit Bars because they contain undeclared FD&C Yellow # 6 and Blue # 1.

    Product
    Spicy Cucumber Fruit Bar , 4 oz. Undeclared FD&C Yellow # 6 and Blue # 1 in clear flexible plastic ingredients: water, cucumber, sugar, orange juice, lime juice, salt, citric acid, chili powder, yellow 5, red 40 UPC Code 8 94163 00210 6
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1356-2013·2013-05-08

    Spicy Mango Dessert Bar Recalled for Undeclared Food Dyes

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Spicy Mango Dessert Bars because the product contains undeclared FD&C Yellow # 6 and Blue # 1.

    Product
    Spicy Mango Dessert Bar , 4 oz. Undeclared FD&C Yellow # 6 and Blue # 1 in clear flexible plastic, ingredients: water, mango, sugar, lime juice, salt, citric acid, chili powder, yellow 5, red 40
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1353-2013·2013-05-08

    Pineapple Fruit Bar Recalled for Undeclared Food Dyes

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz Pineapple Fruit Bars because the packaging fails to list FD&C Yellow #6 and Red #40.

    Product
    Pineapple Fruit Bar, 4 oz. Undeclared FD&C Yellow # 6 and Red # 40 packaged in clear flexible plastic ingredients: water, pineapple, sugar, citric acid, yellow 5 UPC Code 8 94163 00210 6
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1358-2013·2013-05-08

    Guava Fruit Bar Recalled for Undeclared FD&C Red #40 Color

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Guava Fruit Bars because the product contains undeclared FD&C Red #40 and Blue #1 colors.

    Product
    Guava Fruit Bar , 4 oz. Undeclared FD&C Red # 40 in clear flexible plastic, ingredients: water, guava fruit, sugar, tumeric, blue 1, UPC Code 8 94163 00210 6
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1213-2013·2013-05-08

    Encore Medical Recalls 3DKnee e+ Tibial Inserts Due to Labeling Errors

    Encore Medical is recalling five 3DKnee e+ Tibial Inserts because they were shipped with incorrect color-coded labels. The devices were distributed to California and Venezuela.

    Product
    3DKnee e+ Tibial Insert. The insert is used along with the other components that comprise the 3DKnee System.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1365-2013·2013-05-08

    Vanilla Dessert Bar Recalled for Undeclared FD&C Yellow # 6

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Vanilla Dessert Bars because the product contains undeclared FD&C Yellow # 6. The bars were sold in retail stores in Michigan and Indiana.

    Product
    Vanilla Dessert Bar , 4 oz. Undeclared FD&C Yellow # 6 packaged in clear flexible plastic, ingredients: water, sugar, partially hydrogenated palm kernel oil, nonfat milk solids, corn syrup, whey powder, raisins....red 40, yellow 5 UPC Code 8 94163 00220 5
    Category
    Food
    Distribution
    2 states
  • LowFDA (Drugs)·D-301-2013·2013-05-08

    Percocet 10/325 mg Tablets Recalled Due to Foreign Tablet Presence

    Physicians Total Care is recalling one bottle of Percocet 10/325 mg tablets because it contained a foreign Endocet 10/25 mg tablet.

    Product
    Percocet 10/325 mg tablets, 100-count tablets per bottle, Rx only, Dist. By: Physicians Total Care, Tulsa, OK 74146; Mfg. By: Novartis Consumer Health I, Lincoln, NE 68581; NDC 54868-4710-0, Barcode 47101006IHD.
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Food)·F-1360-2013·2013-05-08

    Pina Colada Dessert Bar Recalled for Undeclared Food Dye

    Paleteria Y Neveria La Rosita, LLC is recalling Pina Colada Dessert Bars because the product contains undeclared FD&C Red #40.

    Product
    Pina Colada Dessert Bar , 4 oz. Undeclared FD&C Red # 40 in clear flexible plastic, ingredients: water, sugar, partially hydrogenated palm kernel oil, nonfat milk solids, cream of coconut, whey powder,
    Category
    Food
    Distribution
    2 states
  • LowFDA (Food)·F-1361-2013·2013-05-08

    Strawberry Milk Dessert Bar Recalled for Undeclared FD&C Blue # 1

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Strawberry Milk Dessert Bars sold in Michigan and Indiana due to undeclared FD&C Blue # 1.

    Product
    Strawberry Milk Dessert Bar , 4 oz. Undeclared FD&C Blue # 1 ingredients: water, sugar, partially hydrogenated palm kernel oil, nonfat milk solids, red 40, UPC Code 8 94163 00220 5
    Category
    Food
    Distribution
    2 states
  • LowFDA (Food)·F-1363-2013·2013-05-08

    Strawberry Fruit Bar Recalled for Undeclared FD&C Blue # 1 Ingredient

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Strawberry Fruit Bars sold in Michigan and Indiana because the product contains undeclared FD&C Blue # 1.

    Product
    Strawberry Fruit Bar , 4 oz. Undeclared FD&C Blue # 1 ingredients: water, strawberries, sugar, citric acid, red 40 UPC Code 8 94163 00210 6
    Category
    Food
    Distribution
    2 states
  • LowFDA (Food)·F-1362-2013·2013-05-08

    Bubble Gum Frozen Dessert Bar Recalled for Undeclared Red Dye

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Bubble Gum Frozen Dessert Bars because the product contains undeclared FD&C Red # 3.

    Product
    Bubble Gum Frozen Dessert Bar , 4 oz. Undeclared FD&C Red # 3 packaged in clear flexible plastic, ingredients: water, sugar, citric acid, blue 1 UPC Code 8 94163 00210 6
    Category
    Food
    Distribution
    2 states
  • LowFDA (Food)·F-1364-2013·2013-05-08

    Strawberry Eskimo Dessert Bar Recalled for Undeclared FD&C Blue # 1

    Paleteria Y Neveria La Rosita, LLC is recalling 4 oz. Strawberry Eskimo Dessert Bars because the product contains undeclared FD&C Blue # 1.

    Product
    Strawberry Eskimo Dessert Bar , 4 oz. Undeclared FD&C Blue # 1 packaged in clear flexible plastic, ingredients: water, chocolate coating (coconut oil, sugar, partially hydrogenated coconut and soybean oil, cocoa, corn starch, soy lecithin, etc.) red 40, UPC Code 8 94163 00230 4
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1340-2013·2013-05-01

    All One Multiple Vitamin Powder Recalled for Misleading Dairy Labeling

    All One, Inc. is recalling multiple vitamin powder canisters because the label incorrectly claims 'No Dairy' and 'Certified Vegan' despite containing milk.

    Product
    all One Original Formula Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1339-2013·2013-05-01

    All One Active Senior Multiple Vitamin Powder Recalled for Mislabeling

    All One, Inc. is recalling 796 units of Active Senior Multiple Vitamin & Mineral Powder because the label incorrectly claims 'No Dairy' and 'Certified Vegan' despite containing whey protein isolate.

    Product
    all One Active Senior Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1167-2013·2013-05-01

    Beckman Coulter AU5800 Clinical Chemistry Analyzer Recalled for Software Error

    Beckman Coulter is recalling 490 AU5800 Clinical Chemistry Analyzers due to a software error that may cause the system to misidentify samples and report erroneous patient results.

    Product
    AU5800 Clinical Chemistry Analyzer The Beckman Coulter AU5800 Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate reagents, calibrators, quality control (QC) material and other accessories. This syst
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Food)·F-1321-2013·2013-05-01

    SIB, Inc. Recalls Bakehouse Granola for Undeclared Milk Allergen

    SIB, Inc. is recalling specific lots of Bakehouse Granola because the packaging fails to list milk as an ingredient, posing a risk to consumers with milk allergies.

    Product
    Bakehouse Granola, 12 oz, 340 g Scholar's Inn Bakehouse Granola 16 oz, 454 g All Natural, Baked locally
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1174-2013·2013-05-01

    DePuy Mitek Recalls ORTHOCORD Sutures Due to Inaccurate Strength Labeling

    DePuy Mitek is recalling ORTHOCORD sutures because the instructions for use incorrectly state that Blue sutures retain 100% strength at six weeks.

    Product
    ORTHOCORD One Violet and One Blue Braided Composite Suture with MO-7 Taper Needles, Catalog Number: 223114. For use in general soft tissue approximation, and/or ligation, including orthopedic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide