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.

Which agencies issued them

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.

4926–4950 of 9610

  • HighFDA (Food)·F-1452-2017·2017-02-15

    Taylor Farms Rotini Pasta Salad Recalled for Undeclared Wheat Allergen

    Taylor Farms is recalling 10 oz. Rotini Pasta Salad containers because the label incorrectly identifies the product as mustard potato salad, failing to declare the wheat allergen.

    Product
    Fresh Foods Market Delicatessen Rotini Pasta Salad; Net Wt. 10 oz . (283g) Clamshell package. UPC Code: WO2017019 Perishable; Keep Refrigerated; Distributed by The Kroger Col., Cincinnati, OH
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1177-2017·2017-02-15

    Teleflex Recalls Sheridan Cuffed Tracheal Tubes Due to Labeling Inconsistency

    Teleflex Medical is recalling Sheridan cuffed tracheal tubes because some units are labeled with incorrect sizes, potentially leading to improper airway management.

    Product
    Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A tracheal tube is inserted into a patients mouth or nose for airway management
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Food)·F-1445-2017·2017-02-15

    Annie's Kitchen Vegetable Soup Recalled for Undeclared Wheat Allergen

    Annie's Kitchen is recalling Vegetable Soup because the noodle ingredient contains wheat, which was not declared on the label.

    Product
    Vegetable Soup; Annie's Kitchen; 2966 Stumptown Rd, Ronks, PA 17572 16 FL OZ
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1451-2017·2017-02-15

    Marich Chocolate Caramel Heart Recalled for Unlabeled Almond Allergen

    Marich Confectionery is recalling Chocolate Caramel Hearts because some boxes contained Triple Chocolate Toffee with almonds, which are not listed on the Caramel Heart label.

    Product
    MARICH Premium Chocolates; Chocolate Caramel Heart; Our delicious caramel hearts in rich milk and dark chocolate; Net Wt 4.25 oz. (120g) UPC 797817-44440-9
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1149-2017·2017-02-15

    Stryker Leibinger Recalls Surgical Drainage Accessories Due to Sterility Labeling Error

    Stryker Leibinger is recalling QUINTUBE Monitor Packs and SPG Bulb Drain Systems because non-sterile products were incorrectly labeled as sterile.

    Product
    QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Center Holes (Sterile) Accessories to TLS Surgical Drainage System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1150-2017·2017-02-15

    Stryker Leibinger Recalls Non-Sterile Medpor Implant Sizer Sets Due to Labeling Error

    Stryker Leibinger is recalling specific non-sterile Medpor implant sizer sets because they were incorrectly labeled as sterile. The recall covers 619 units distributed in the US and several international countries.

    Product
    9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design M Malar Sizer Set (Silicone, Non-Sterile) 9952 Extended Contoured, Malar Sizer Set (Silicone, Non-Sterile) 85000 Petite Nasal Dorsum Sizer Set (Silicone, Non-Sterile) Accessories to Medpor Implants
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·013-2017·2017-02-15

    Century Packing Recalls Chicken Sausage Products Due to Undeclared MSG

    Century Packing Corp. is recalling approximately 999,419 pounds of chicken sausage products because they contain undeclared monosodium glutamate (MSG).

    Product
    Century Packing Corp. — Century Packing Corp. Recalls Chicken Sausage Products Due To Misbranding
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-1146-2017·2017-02-15

    Thayer MiniSpacer MDI Adapter Recalled for Incorrect Labeling

    Thayer Medical Corporation is recalling 2,550 MiniSpacer MDI adapters because the insert and case labels incorrectly state the connection size.

    Product
    Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with 15mm O.D./I.D. Connections, Reference no. 1543A. The 15 mm Dual Spray MiniSpacer with Counter Incrementing Actuator is a non-sterile, single-use item, intended to dispense aerosolized medication into a b
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1145-2017·2017-02-15

    FDA Recalls Hotline Blood and Fluid Warmers for Incorrect Language Labeling

    Smiths Medical ASD, Inc. is recalling 33 Hotline Blood and Fluid Warmers distributed to Finland because they included Greek and Danish labeling instead of the required Finnish labeling.

    Product
    HOTLINE Blood and Fluid Warmer, Mole l HL-90. Designed for use with the Hotline Fluid Warming Set (L-80, L-70 and L-70N) to warm blood and intravenous (I.V.) fluids and deliver them to the patient's intravenous access site at normothermic temperatures under gravity flow conditio
    Category
    Medical Device
    Distribution
    0 states
  • ModerateNHTSA·17V091000·2017-02-10

    Heartland Recalls 2017 Sundance Trailers for Missing Weight Rating Label

    Heartland is recalling 2017 Sundance recreational trailers because the Federal Certification label may be missing the Gross Vehicle Weight Rating, which could lead to overloading.

    Product
    HEARTLAND — HEARTLAND SUNDANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1372-2017·2017-02-08

    King's Pastry Recalls Cappuccino Carnival Cake for Undeclared Hazelnut

    King's Pastry is recalling frozen Cappuccino Carnival Cakes because the product contains undeclared hazelnut and/or tree nuts, posing a risk to consumers with allergies.

    Product
    Cappuccino Carnival Cake (12"x 16"), 2 kg. Frozen Product Code: 10081 UPC: 1068596110814
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1371-2017·2017-02-08

    King's Pastry Recalls Chocolate Lava Cakes Due to Undeclared Hazelnut

    King's Pastry is recalling Bakewell Desserts Chocolate Lava Cakes because they contain undeclared hazelnut and/or tree nuts. Consumers should not eat these products.

    Product
    Bakewell Desserts Chocolate Lava Cake (4" x4"), 113g Product Code: 10309 UPC: 68596110392
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1386-2017·2017-02-08

    Los Chileros Basil Pesto Recalled for Missing Milk Allergen Labeling

    Los Chileros De Nuevo Mexico, LLC is recalling Basil Pesto because the ingredient list failed to disclose milk, a major allergen, despite containing Parmesan Cheese.

    Product
    Los Chileros, Basil Pesto, Net Wt. 6 oz. (170g). plastic shell container. Keep Refrigerated
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1119-2017·2017-02-08

    Siemens Recalls IMMULITE PSA Kits Due to Negative Bias

    Siemens Healthcare Diagnostics is recalling IMMULITE PSA kits worldwide because patient samples show an average negative bias of approximately -22%.

    Product
    IMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LKUP1, SMN 10380956 (OUS Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers for the quantitative measurement of prostate-specific antigen (PSA) in huma
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1125-2017·2017-02-08

    Covidien Nellcor SpO2 Forehead Sensor Recalled for Latex Labeling Error

    FDA is recalling 7,453 units of the Covidien Nellcor SpO2 Forehead Sensor because the label incorrectly states the product is latex-free, while the headband contains latex.

    Product
    Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10; The Covidien Nellcor¿ Forehead SpO2Sensor, model RS10, is indicated for use when continuous non-invasive arterial oxygen saturation and pulse rate monitoring are required for patients weighing more than 40 kg.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1117-2017·2017-02-08

    Ortho-Clinical VITROS Na+ Slides Recalled for Potential Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Na+ Slides because they may produce biased results if stored on the analyzer for 10 days after minimum warm-up.

    Product
    VITROS Na+ Slides, (UPN 10758750004812) For in vitro diagnostic use only. VITROS Na+ Slides quantitatively measure sodium (Na+) concentration in serum, plasma, and urine using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1115-2017·2017-02-08

    Zimmer Biomet Recalls Vanguard Total Knee System Femoral Components Due to Labeling Errors

    Zimmer Biomet is recalling Vanguard Total Knee System femoral components because packaging labels may incorrectly identify the size or side of the implant.

    Product
    Vanguard Total Knee System Vanguard Open Box Femoral Components Item Number: 183100 Description: VNGD PS OPEN INTL FEM RT 55 Item Number: 183102 Description: VNGD PS OPEN INTL FEM-RT 57.5 Item Number: 183104 Description: VNGD PS OPEN INTL FEM RT 60 Item Number: 183106
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1114-2017·2017-02-08

    Zimmer Biomet Recalls Mislabelled Orthopedic Salvage System Tibial Bodies

    Zimmer Biomet is recalling 16 Orthopedic Salvage System tibial bodies because labels incorrectly identify them as AVL Modular Proximal Tibia components.

    Product
    Orthopedic Salvage System (OSS) 9cm prosthesis, knee, femorotibial, constrained, cemented, metal/polymer Knee System Tibial Bodies
    Category
    Medical Device
    Distribution
    8 states
  • SevereUSDA FSIS·011-2017·2017-02-07

    Ukrop's Recalls Chili Flavored Soups Due To Undeclared Allergens

    Ukrop's Homestyle Foods is recalling approximately 45 pounds of beef and chicken chili flavored soups because they contain undeclared milk, wheat, and soy.

    Product
    Ukrop's Homestyle Foods — Ukrop’s Homestyle Foods Recalls Beef and Chicken Chili Flavored Soup Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1341-2017·2017-02-01

    Farm to Market Foods Recalls Smoked Ham Dinner for Undeclared Peanuts

    Farm to Market Foods is recalling Smoked Ham Dinner #1977 Holiday products in Texas due to undeclared peanuts.

    Product
    Farm to Market Foods Smoked Ham Dinner #1977 Holiday Ingredients: Smoked Spiral Diced Ham, Mashed Potatoes, Orange Cranberry Relish, Broccoli Rice Casserole, Green Bean Casserole. Keep Refrigerated at 38 Deg F or Less UPC: 617037959081
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1092-2017·2017-02-01

    Roche Tina-Quant CRP Latex Test System Recalled for Low Results

    Roche is recalling Tina-Quant CRP Latex High Sensitive test kits due to potential under-recovery of results, which may lead to incorrect cardiovascular risk assessments.

    Product
    Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High Sensitive) The Tina-Quant CRP (Latex) High Sensitive Immunoturbidimetric assay is for the in-vitro quantitative determination of C-reactive protein (CRP) in human serum and plasma on Roche automated clinical che
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1338-2017·2017-02-01

    Gonsalves Sugar Coated Almonds Recalled for Undeclared Wheat and Dyes

    The Henry Gonsalves Co. is recalling Gonsalves Sugar Coated Almonds because the product contains undeclared wheat and artificial dyes.

    Product
    Gonsalves Sugar Coated Almonds, Net Wt. 12 oz. Distributed by The Gonsalves Company, Smithfield, RI 02917 UPC number 20539-64550
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1367-2017·2017-02-01

    Harris Teeter Recalls Everroast Chicken Caesar Wrap for Undeclared Fish

    Harris Teeter is recalling Everroast Chicken Caesar Wraps because they contain an undeclared fish allergen. The product was sold in eight states.

    Product
    Everroast Chicken Caesar Wrap, UPC: 72036-95828, in clear flexible plastic.
    Category
    Food
    Distribution
    8 states