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.

7326–7350 of 9611

  • ModerateFDA (Devices)·Z-1732-2014·2014-06-18

    Teleflex Recalls RUSCH Easy Cath Coude Kits Due to Incorrect Catheter Type

    Teleflex Medical is recalling 1,000 RUSCH Easy Cath Coude Kits because they were packaged with straight catheters instead of the required curved ones.

    Product
    RUSCH Easy Cath Coude Kit, 10 FR, Rx Only, Sterile, Distributed by: Teleflex Medical, Research Triangle Park, NC 27708. A tubular device that is inserted through the urethera and is used to pass fluids to or from urinary tracts.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Food)·F-2010-2014·2014-06-18

    Mandelin Recalls Marzipan for Undeclared Yellow Dyes 5 and 6

    Mandelin Inc is recalling marzipan products containing undeclared Yellow #5 and #6 dyes. The affected items were distributed in California, Kentucky, and Colorado.

    Product
    Marzipan - Pink, Orange and Green; Packed in 1 lb, (16 oz.) plastic containers and and 10.5 lb. 4.76 kg) pails. Ingredient: Sugar, almonds, potassium sorbate, oil of bitter almonds. Mandelin: California Almonds and Almond Pastes, Wasco California 93280
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1735-2014·2014-06-18

    Ortho-Clinical VITROS 5600 Integrated System Recalled for Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems due to a software issue that may cause biased results when using Multiple Window codes.

    Product
    VITROS 5600 Integrated System, Product Code/Catalog Number 6802413 for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1641-2014·2014-06-18

    Smiths Medical Recalls Mislabelled Portex Low Dead Space Connectors

    Smiths Medical ASD, Inc. is recalling one lot of Portex Low Dead Space Connectors with Sideport because 3.0mm devices were packaged and labeled as 3.5mm.

    Product
    Portex Low Dead Space Connector with Sideport, 3.5mm Product Usage: The connector is used to attach the endotracheal tube to the patient breathing circuit. The low dead space connector minimizes mechanical dead space and subsequent carbon dioxide rebreathing. The connector's
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-1787-2014·2014-06-18

    Beekley Spots Light Image O-Spots Recalled for Mislabeled Dispenser

    Beekley Corporation is recalling 81 boxes of Light Image O-Spots for mammography because the dispensers were mislabeled as S-Spots.

    Product
    Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product Usage: To identify raised moles in Mammography
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Food)·F-2008-2014·2014-06-11

    Rockman Raw Peanuts Recalled for Mold and Missing Allergen Labeling

    Rockman Company USA is recalling raw peanuts due to mold contamination and missing allergen, nutrition, and ingredient information.

    Product
    Rockman (Brand) Raw Peanuts with Red Skin, 12 oz. Packaged in plastic pouch. 12oz/60bags/carton. Labeled as "PEANUT" on packaging. Product labeling reads in part: "ROCKMAN***PEANUT N.W.: 12 OZ (342G)***DISTRIBUTED BY: ROCKMAN (AUSTRALIA) PTY LTD.***AUSTRALIA***PRODUCT OF
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Drugs)·D-1359-2014·2014-06-11

    CareFusion Recalls Surgical Scrub Brushes With Low Iodine Levels

    CareFusion is recalling surgical scrub brushes because the available iodine content is lower than stated on the label.

    Product
    CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 9% Povidone-iodine (USP) Surgical Hand Scrub; CareFusion, Vernon Hills, IL 60061 USA, NDC 57613-003-18
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1360-2014·2014-06-11

    CareFusion Recalls Surgical Scrub Brushes With Low Iodine Levels

    CareFusion is recalling surgical scrub brushes because the available iodine content is lower than stated on the label.

    Product
    CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15% Povidone-iodine (USP) Surgical Hand Scrub; CareFusion, Vernon Hills, IL 60061 USA, NDC 57613-013-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1681-2014·2014-06-11

    Synthes XRL Medium Trial Central Body Recalled for Incorrect Dimension Etching

    Synthes, Inc. is recalling two lots of the Synthes XRL Medium Trial-Central Body device because they were incorrectly etched with the wrong height dimensions.

    Product
    Synthes XRL Medium Trial - Central Body, an instrument used as part of the Synthes XRL System, a vertebral body replacement device. For spinal surgery. The Synthes XRL device is intended to be used with the Synthes supplemental internal fixation systems (e.g., USS, including MA
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-2009-2014·2014-06-11

    Rockman Skinless Peanuts Recalled for Mold and Mislabeling

    Rockman Company USA Inc. is recalling skinless peanuts due to mold contamination and mislabeling. The affected product was distributed in several US states.

    Product
    Rockman (Brand) Skinless Peanut, 12 oz. Description: blanched skinless peanut. Packaged in plastic pouch. 12oz/60bags/carton. Product labeling reads in part: "ROCKMAN***SKINLESS PEANUT 12 0Z (342G)***DISTRIBUTED BY: ROCKMAN (AUSTRALIA) PTY LTD.***AUSTRALIA***PRODUCT OF C
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1697-2014·2014-06-11

    Integra Newdeal SURFIX Screws Recalled for Packaging Labeling Error

    Integra LifeSciences is recalling specific lots of SURFIX locking screws because some 22mm units were mislabeled as 30mm units.

    Product
    Integra Newdeal SURFIX Fixed Angle Locking Screw 3.5mm x 22mm (catalog number 285322S) and 3.5mm x 30mm (catalog number 285330S). Screws are provided in different diameters and lengths and are used to anchor various sizes and shapes of bone fixation plates when treating bone frac
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1720-2014·2014-06-11

    Small Bone Innovations Recalls Non-Sterile RingFIX Olive Wires

    Small Bone Innovations is recalling non-sterile RingFIX Olive Wires because they were packaged with the wrong internal component.

    Product
    SBi RingFix Olive Wires Product Usage: These are temporary devices indicated for: osteosynthesis of fractures with small osteoarticular fragments, fixation of open and closed fractures, arthrodesis, sepsis, limb lengthening, and osteotomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1675-2014·2014-06-11

    Integra Licox Test Kit Recall for Erroneous Calibration Messages

    Integra LifeSciences is recalling Licox Test Kits that may display false calibration failure messages or out-of-range results when used with specific PtO2 monitors.

    Product
    Integra Licox Test Kit REF BC10R Rx Only An accessory provided for use with the LCXO2 and AC31 PtO2 Monitors. It provides users with a secondary means to verify the monitor's PtO2 state-of-calibration (but does not provide calibration) when needed by providing a specific elec
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·F-1985-2014·2014-06-11

    Gavina Dark Whole Bean Coffee Recalled for Mislabeling as Decaffeinated

    F. Gavina & Sons Inc. is recalling 29 units of Gavina Northwest Blend Dark Whole Bean Coffee because it was mislabeled as decaffeinated.

    Product
    Gavina Northwest Blend Dark Whole Bean Bag Net Wt. 5lb, Product label reads in part "***085895***DECAF EUROPEAN BLEND 5LBS WHOLEBEAN BAG***"
    Category
    Food
    Distribution
    2 states
  • LowFDA (Food)·F-1995-2014·2014-06-11

    American Licorice Company Recalls Redvines Fruit Vines Bites for Labeling Error

    American Licorice Company is recalling Redvines Fruit Vines Bites because the packaging incorrectly lists the sodium content as 35g instead of 35mg.

    Product
    REDVINES FRUIT VINES Bites Strawberry ARTIFICIALLY FLAVORED NET WT, 2 oz (57G) Nutrition Facts: ***Sodium 35g***ALLERGEN INFORMATION: CONTAINS WHEAT***AMERICAN LICORICE COMPANY, UNION CITY, CA 94587 UPC 0 41364 82006 4
    Category
    Food
    Distribution
    9 states
  • LowFDA (Food)·F-1994-2014·2014-06-11

    American Licorice Company Recalls Redvines Fruit Vines Bites Due to Labeling Error

    American Licorice Company is recalling Redvines Fruit Vines Bites Cherry because the packaging incorrectly lists sodium content as 35g instead of 35mg.

    Product
    REDVINES FRUIT VINES Bites Cherry ARTIFICIALLY FLAVORED NET WT, 2 oz (57G) Nutrition Facts: ***Sodium 35g***ALLERGEN INFORMATION: CONTAINS WHEAT***AMERICAN LICORICE COMPANY, UNION CITY, CA 94587 UPC 0 41364 82001 9
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1972-2014·2014-06-04

    Price Chopper Tuscan White Bean Hummus Recalled for Undeclared Milk

    Golub Corporation is recalling Price Chopper brand Tuscan White Bean Hummus due to a labeling mix-up that resulted in an undeclared milk allergen.

    Product
    Price Chopper brand Hummus TUSCAN WHITE BEAN, NET WT. 10 OZ. Labels applied to clear plastic container with black rim on lid.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1971-2014·2014-06-04

    Organic Traditions Dark Chocolate Sacha Inchi Seeds Recalled for Undeclared Milk

    Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Sacha Inchi Seeds because the product contains undeclared milk, a major food allergen.

    Product
    Organic traditions DARK CHOCOLATE SACHA INCHI SEEDS***DAIRY & SUGAR FREE 80% DARK CHOCOLATE; Pack sizes: 3.5oz/100g, UPC 8 54260 00709 1; 5.3 oz (150g), UPC 8 54260 00718 3; 12kg bulk boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1974-2014·2014-06-04

    Borden Vitamin D Milk Recalled for Excess Vitamin D Content

    Borden Dairy Co. is recalling Vitamin D Milk because it contains more than double the labeled amount of Vitamin D.

    Product
    Vitamin D Milk GRADE A PASTEURIZED HOMOGENIZED; 4-oz paper, 300-gal totes, Gallons, 1/2 gallons, pints, quarts, paper 1/2 pints, 5-gal dispense bags. INGREDIENTS: MILK AND VITAMIN D3. Product is sold under the following brand names and UPC codes: American Fare: Gal: 0 72000 1523
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Food)·F-1973-2014·2014-06-04

    Price Chopper Roasted Garlic Hummus Recalled for Labeling Errors

    Golub Corporation is recalling Price Chopper brand Roasted Garlic Hummus due to a mix-up in nutrition panel and ingredients labeling.

    Product
    Price Chopper brand Hummus ROASTED GARLIC, NET WT. 10 OZ. Labels applied to clear plastic container with black rim on lid.
    Category
    Food
    Distribution
    6 states
  • LowUSDA FSIS·033-2014·2014-05-29

    Boulder Natural Meats Recalls Chicken Breasts Due to Gluten Free Label Error

    Boulder Natural Meats is recalling approximately 363 pounds of boneless skinless chicken breasts because the front label incorrectly stated the product was gluten free, despite containing wheat.

    Product
    Recall Notification Report 033-2014 (Boneless Skinless Chicken Breasts)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1957-2014·2014-05-28

    Emparedados Boricua Chicken and Cheese Sandwiches Recalled for Undeclared Eggs

    Emparedados Boricua is recalling 136 units of Pollo & Queso sandwiches in Puerto Rico due to undeclared eggs.

    Product
    "Emparedados Boricua, Pollo & Queso (Chicken & Cheese), Net Wt. 6.5 oz, Elaborated and Distributed by Emparedados Boricua, Bayamon, PR, 00956"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1961-2014·2014-05-28

    Blue Bunny Ice Cream Recalled for Unlabeled Egg Ingredient

    Wells Enterprises is recalling Blue Bunny Premium Ice Cream because it may contain egg, which is not listed on the ingredient label.

    Product
    Blue Bunny Premium Ice Cream, Bordeaux Cherry Chocolate, 1.75 quart. Packaged in 4/56-oz carton cases. Item # 745152, UPC 070640034123. Manufactured by Wells Enterprises, Inc., Le Mars, IA.
    Category
    Food
    Distribution
    3 states