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.

3326–3350 of 9607

  • HighFDA (Food)·F-1837-2018·2018-08-29

    Graeter's Key Lime Pie Ice Cream Recalled for Wheat Mislabeling

    Graeter's is recalling 4,056 pints of Key Lime Pie ice cream because it is labeled gluten-free but contains wheat.

    Product
    Graeter's HANDCRAFTED French Pot ICE CREAM, Limited Edition KEY LIME PIE**ONE PINT (473 ml)**Nutrition Facts**GLUTEN FREE**INGREDIENTS: CREAM, MILK, CANE SUGAR, GRAHAM PIE PIECES, WHEAT FLOUR**CONTAINS:MILK, EGG, WHEAT,& SOY**Manufactured by: Graeter's Ice Cream, Cincinnati, OH**
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-2883-2018·2018-08-29

    Smith & Nephew Recalls Mispackaged Genesis II Knee Prosthesis Components

    Smith & Nephew is recalling two lots of Genesis II knee prosthesis components because they were packaged with the wrong size and side.

    Product
    GENESIS II NON-POROUS CRUCIATE RETAINING FEMORAL COMPONENT, SIZE 6 RIGHT, REF 71420026 Knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-1843-2018·2018-08-29

    Asian Gourmet Spicy Chili & Garlic Sauce Recalled for Labeling Error

    Asian Gourmet Spicy Chili & Garlic Sauce is being recalled because the sodium values on the label are not consistent with the current value.

    Product
    ASIAN GOURMET SPICY Chili & Garlic Sauce, NET WT. 12.3 OZ (380g), Distributed by Asian Gourmet 313 Iron Horse Way, Providence, RI 02908 USA, Product of Costa Rica
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2889-2018·2018-08-29

    Ortho Kinematics Recalls Vertebral Motion Analyzer Software Due to Report Error

    Ortho Kinematics is recalling the Vertebral Motion Analyzer (VMA) software because a bug caused errors in the Radiological Read Report.

    Product
    Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2881-2018·2018-08-29

    Back 2 Basics Recalls Dymaxeon 5.5 Curved Spinal Rods Due to Labeling Error

    Back 2 Basics Direct LLC is recalling 10 Dymaxeon 5.5 Curved Rods because packages labeled as 110mm may contain 100mm rods.

    Product
    Dymaxeon 5.5 Curved Rod Size 5.5 x 110mm (Yellow), Model Number 06.6441B Product Usage: The Dymaxeon Spine System is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2880-2018·2018-08-29

    In2Bones Recalls CoLink Lapidus Plates Due to Incorrect Laser Marking

    In2Bones USA, LLC is recalling 48 units of CoLink Lapidus Plates because right and left plates were laser marked incorrectly.

    Product
    CoLink(TM) Lapidus Plate XP, +2 mm, Left, REF P40 ST265, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLink¿ Plating System is indicated for stabilization and fixation of fractures, revision procedures, joint fusion, osteotomies and reconstruction of the small bones
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1842-2018·2018-08-29

    Tropical Pepper Co. Crushed Chili Pepper Sauce Recalled for Labeling Error

    Alimentos Kamuk Internacional is recalling Tropical Pepper Co. Crushed Chili Pepper Sauce because the sodium values on the label are inconsistent with the current value.

    Product
    TROPICAL PEPPER CO. Crushed Chili Pepper Sauce, 11.5 FL. OZ. (325ml), PRODUCT OF COSTA RICA, Packed Exclusively for: H.L. Benndorf Corp. Medford, NJ 08055
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2879-2018·2018-08-29

    In2Bones Recalls CoLink Lapidus Plates Due to Incorrect Laser Marking

    In2Bones USA, LLC is recalling 47 CoLink Lapidus Plate XP units because right and left plates were incorrectly laser-marked.

    Product
    CoLink(TM) Lapidus Plate XP, +2 mm, Right, REF P40 ST165, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLink¿ Plating System is indicated for stabilization and fixation of fractures, revision procedures, joint fusion, osteotomies and reconstruction of the small bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2886-2018·2018-08-29

    Arrow Pediatric Central Venous Catheter Kit Recalled for Labeling Error

    Arrow International is recalling 166 kits of pediatric central venous catheters because the packaging incorrectly identifies the catheter length.

    Product
    Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, Cat. No. AK-22502 Product Usage: The multiple-lumen catheter permits venous access to the central circulation of pediatric patients. The ARROWg+ard antimicrobial surface is i
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-2891-2018·2018-08-29

    Ortho Kinematics Recalls Vertebral Motion Analyzer Software Due to Report Errors

    Ortho Kinematics is recalling VMA software versions 2.3.239 through 2.3.254 because administrative errors caused incorrect data in radiological and VMA reports.

    Product
    Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254. Product Usage: VMA software is a quantitative imaging software application intended to be used to process digital image files.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2920-2018·2018-08-29

    Euro Diagnostica Anti-Cardiolipin ELISA Kits Recalled for Labeling Error

    Euro Diagnostica AB is recalling Anti-Cardiolipin ELISA kits due to incorrect labeling. The kits were incorrectly labeled as 'Manufactured by DiaSorin' instead of 'Distributed by DiaSorin.'

    Product
    is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of IgG and IgM autoantibodies specific for the phospholipid cardiolipin in human serum and EDTA, lithium heparin or citrated plasma. It is intended to assess of anti-cardiolipin IgG autoanti
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-2919-2018·2018-08-29

    Euro Diagnostica Anti-Ro ELISA Kits Recalled for Incorrect Labeling

    Euro Diagnostica is recalling Anti-Ro (SS-A) ELISA kits due to incorrect labeling. The label incorrectly states 'Manufactured by DiaSorin' instead of 'Distributed by DiaSorin'.

    Product
    is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of autoantibodies specific for Anti-Ro (SS-A) antigen in human serum or plasma. EDTA, lithium heparin, citrated plasma. It is intended to aid in the diagnosis of systemic rheumatic diseases,
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-2922-2018·2018-08-29

    Euro Diagnostica Scl-70 ELISA Kits Recalled for Labeling Error

    Euro Diagnostica AB is recalling four Scl-70 ELISA kits due to incorrect distribution labeling. The kits were manufactured by DiaSorin but incorrectly labeled as manufactured by them.

    Product
    is a qualitative indirect enzyme immunoassay enzyme-linked immunosorbent assay (ELISA) for the detection, in human serum or plasma, of antibodies specific for the Scl-70 antigen. The test is intended to as an aid to the diagnosis of scleroderma and is not definitive in isolation.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-2921-2018·2018-08-29

    Euro Diagnostica Anti-Cardiolipin ELISA Kits Recalled for Labeling Error

    Euro Diagnostica AB is recalling six lots of anti-cardiolipin ELISA kits due to an incorrect distribution label. The kits were distributed in Minnesota.

    Product
    is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of IgG and IgM autoantibodies specific for the phospholipid cardiolipin in human serum and EDTA, lithium heparin or citrated plasma. It is intended to assess anti-cardiolipin IgM autoantibod
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·18V566000·2018-08-28

    Blue Bird Recalls School Buses for Missing Child Restraint Warning Labels

    Blue Bird is recalling 2019-2020 Vision and All American school buses because certain child restraint seats may be missing a required warning label on the lower strap.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1826-2018·2018-08-22

    Mediterranean Salad Vegan Recalled for Undeclared Milk Allergen

    Market of Choice Inc is recalling pre-packaged Mediterranean Salad Vegan because milk is listed in the ingredients but not in the 'Contains' statement.

    Product
    Mediterranean Salad Vegan, pre-packaged. UPC 0 211004 706991.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1827-2018·2018-08-22

    BulkSupplements.com Recalls Glucosamine Sulfate Potassium for Undeclared Shellfish

    Hard Eight Nutrition LLC is recalling two lots of Glucosamine Sulfate Potassium because the product labels failed to declare shellfish as an ingredient.

    Product
    BulkSupplements.com Glucosamine Sulfate Potassium; 100 grams, 250 grams, 500 grams, 1 kilogram; Stand up zipper pouch bags. Directions: As a dietary supplement, take 1000 mg (scant 1/4 tsp) up to three time daily, or as directed by a physician. Distributed exclusively by:
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1814-2018·2018-08-22

    Confidence Nitro-Cross 60s Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Nitro-Cross 60s supplements due to undeclared ingredients including HPMC and Titanium Dioxide.

    Product
    FP0292 Confidence Nitro-Cross 60s, UPC# 8 92483 00155 7
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1823-2018·2018-08-22

    Severino Cheese Raviolini Recalled for Undeclared Eggs on Bottom Label

    Severino Pasta Manufacturing is recalling Cheese Raviolini because the bottom label incorrectly identifies the product as Rigatoni and omits eggs, creating an allergen mislabeling risk.

    Product
    Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units x 9 oz per case. Expiration March 2019.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2822-2018·2018-08-22

    Nico Corp. Recalls Mislabeled Sterile Shepherd's Hook Accessories

    Nico Corp. is recalling 204 sterile Shepherd's Hook accessories because they were shipped with incorrect transport labels instead of product labels.

    Product
    NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath device Part Number: NN-8024
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2821-2018·2018-08-22

    Zimmer Biomet Recalls Echo Hip Stems Due to Potential Component Comingle

    Zimmer Biomet is recalling 12 Echo Bi-Metric Hip Stems because they may have been mixed with a different model. The error could extend surgery time.

    Product
    ECHO Bi-Metric Hip System, Reduced Proximal Profile, Standard 135o neck, item number 192414. orthopedic hip prosthesis femoral stem
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Food)·F-1772-2018·2018-08-22

    Sunny Side Farms Ice Cream Recalled for Flavor Mismatch

    Super Store Industries is recalling Sunny Side Farms Peanut Butter Cup Ice Cream because some containers are filled with Butter Pecan ice cream.

    Product
    Sunny Side Farms Peanut Butter Cup Ice Cream; 48 oz. carton, 1.5 QTS (1.42L) UPC: 7-17544-20740 5 Allergens for Peanut Butter Cup: Milk, Peanuts, Soy, Coconut. Allergens for Butter Pecan: Milk, Pecans Both packages include the following statement: While best practic
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-2786-2018·2018-08-22

    Clarity 10SG Urinalysis Strips Recalled for Analyzer Incompatibility

    Clarity Diagnostics is recalling specific lots of Clarity 10SG Urinalysis Strips because they lack a Canister Code Bar Code Label, making them incompatible with Clarity Urocheck 120 Urine Analyzers.

    Product
    Clarity Urocheck 10SG Urinalysis Strips, Model # DTG-10SG Product Usage: Clarity 10SG Urinalysis Reagent Strips (Urine) are for the qualitative and semi-quantitative detection of the following analytes in urine: Glucose, Bilirubin, Ketone (Acetoacetic acid), Specific Gravity,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2827-2018·2018-08-22

    Tosoh Bioscience Recalls AIA Analyte Application Manual CDs

    Tosoh Bioscience is recalling 9 AIA Analyte Application Manual CDs due to unapproved product labeling. The CDs were distributed to six US states.

    Product
    Tosoh Bioscience AIA Analyte Application Manual (AAM) CD Part Number: 997027 CD contains analyte application manuals for 47 analyte reagent packs for use with the Tosoh AIA (Automated Immuno-Assay) family of analyzers. Each analyte application manual includes a reference sect
    Category
    Medical Device
    Distribution
    6 states
  • LowFDA (Drugs)·D-1076-2018·2018-08-22

    Acne Treatment Pads Recalled for Subpotent Salicylic Acid Levels

    Huijing (Shanghai) Bio-tech Co., Ltd. is recalling Acne Treatment Pads because the active ingredient level does not match the label.

    Product
    Acne Treatment Pads (2% salicylic acid), packaged in a 50-count jar, OTC, Distributed by: Greenbrier International, Inc. 500 Volvo Parkway, Chesapeake, VA 23320, NDC 71537-001-02
    Category
    Drug
    Distribution
    1 state