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.

2801–2825 of 9607

  • ModerateFDA (Food)·F-1337-2019·2019-05-15

    U.S. Tov Recalls Dragonfly Dehydrated Guava for Undeclared Sulfites

    U.S. Tov, Inc. is voluntarily recalling 68 units of Dragonfly Dehydrated Guava because the product contains undeclared sulfites.

    Product
    Dragonfly Dehydrate Guava Ing: Guava, Sugar, Salt Net Wt: 5.25 ozs 150g Distributed by: U.S. Trading Company Product of Thailand Item Number:37115 UPC: 721557371152
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-1297-2019·2019-05-15

    Elekta Unity Systems Recalled for Missing Contrast Agent Warnings

    Elekta Limited is recalling nine Elekta Unity systems because the user manual lacks a warning regarding the administration of unvalidated contrast agents.

    Product
    Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy treatments and stereotactic radiation treatments of malignant and benign diseases anywhere in the body as determined by a licensed medical practitioner in acco
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1315-2019·2019-05-08

    Fannie May Pixies Recalled for Missing Pecan Allergen Labeling

    Fannie May Confections Brands, Inc. is recalling Pixies Caramel and Pecan Clusters because the outer holiday wrap fails to declare pecans, a major allergen.

    Product
    Fannie May Pixies , Caramel and Pecan Clusters covered in Milk Chocolate 14 oz. Box - 12 units per case
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1316-2019·2019-05-08

    Trader Joe's Saucy Scallops Recalled for Unlabeled Crustacean Allergen

    Frial SAS is recalling Trader Joe's Saucy Scallops with Mushrooms because the scallop flavor contains low levels of crustaceans not listed on the label.

    Product
    Trader Joe's Saucy Scallops with Mushrooms, NET Wt. 16 oz. (1 LB) 454 g UPC 0093 0390 24 units per case Product of France Dist. and sold exclusively by: Trader Joe's Monrovia, CA 91016
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-1314-2019·2019-05-08

    Tom Sturgis Little Ones Pretzels Recalled for Undeclared Milk Allergen

    Tom Sturgis Pretzels, Inc. is recalling Little Ones Pretzels because some bags contain a milk allergen not listed on the label.

    Product
    Little Ones Pretzels¿ 4.5lb, 1 polyethylene bag per corrugated container .
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1324-2019·2019-05-08

    Stanganellis Pumpkin Cake Roll Recalled for Missing Soy Allergen Labeling

    Spagel Brothers, Inc. is recalling Stanganellis Pumpkin Cake Roll because the packaging failed to list soy as an ingredient.

    Product
    Stanganellis Italian Foods, Pumpkin Cake Roll, Net Wt. 24 oz. . One pie per package . Box.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1234-2019·2019-05-08

    Siemens ADVIA Centaur aTG Test Kits Recalled for Positive Bias

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur aTG test kits due to positive bias in anti-thyroglobulin results compared to WHO standards.

    Product
    SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN): 10492399
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1223-2019·2019-05-08

    Matrix Surgical Recalls 46 OmniPore Implants Due to Mislabeling

    Matrix Surgical Holdings is voluntarily recalling 46 OmniPore Surgical Implants due to product mislabeling. The recall covers units distributed in the US and several international countries.

    Product
    OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: OmniPore Surgical Implants in block, sheet, and anatomical shapes are intended for nonweight bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. OmniPore Surgi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1233-2019·2019-05-08

    Siemens ADVIA Centaur aTG Test Kits Recalled for Positive Bias

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur aTG test kits due to positive bias in anti-thyroglobulin results compared to WHO standards.

    Product
    Siemens ADVIA Centaur aTG (100 test kit) Siemens Material Number (SMN): 10492398
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1326-2019·2019-05-08

    Wawa Iced Tea Less Sugar Recalled for Missing Phenylketonuria Warning

    Wawa, Inc. is recalling Wawa Iced Tea Less Sugar bottles because the label fails to list the required phenylketonuria warning and does not identify Aspartame as an ingredient.

    Product
    Wawa Iced Tea Less Sugar, Net weight/number of units per package: 12 FL OZ. , Package type: Bottle Units per case: 24, Expiration date: April 29, 2019 (APR/29/19)
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1224-2019·2019-05-08

    Matrix Surgical Recalls 42 OmniPore Implants Due to Mislabeling

    Matrix Surgical Holdings is recalling 42 OmniPore Surgical Implants due to product mislabeling. The recall covers units distributed in the US and several international countries.

    Product
    OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: OmniPore Surgical Implants in block, sheet, and anatomical shapes are intended for nonweight bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. OmniPore Surgi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1254-2019·2019-05-08

    Randox G-6-PDH Deficient Control Recalled for Incorrect Target Values

    Randox Laboratories is recalling 14 kits of G-6-PDH Deficient Control because the target values and ranges in specific lots are incorrect.

    Product
    G-6-PDH Deficient Control (G-6-PDH CONTROL D), Catalogue Number PD2617 Product Usage: This product is intended for in vitro diagnostic use, in the quality control of Glucose-6-Phosphate Dehydrogenase in erythrocytes
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1255-2019·2019-05-08

    Randox G-6-PDH Normal Control Recalled for Incorrect Target Values

    Randox Laboratories is recalling 10 kits of G-6-PDH Normal Control because the target values and ranges in specific lots are incorrect.

    Product
    G-6-PDH Normal Control (G-6-PDH CONTROL N), Catalogue Number PD2618 Product Usage: This product is intended for in vitro diagnostic use, in the quality control of Glucose-6-Phosphate Dehydrogenase in erythrocytes
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Drugs)·D-1280-2019·2019-05-08

    Dermoplast Anesthetic Spray Recalled for Incorrect Net Weight Labeling

    Advantice Health is recalling Dermoplast Anesthetic Spray canisters because some full cases contain cans labeled with an incorrect net weight of 2.75 oz instead of 2.0 oz.

    Product
    Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters, 20%, 0.5%; full case of 12-2 oz. cans only; Distributed by Moberg Pharma North America LLC, Cedar Knolls, NJ 07927; Product Code 80-6802; Case UPC 1 03 16864 68002 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1279-2019·2019-05-08

    Dermoplast Anesthetic Spray Recalled for Incorrect Net Weight Labeling

    Advantice Health is recalling Dermoplast Anesthetic Spray canisters because the label incorrectly states the net weight as 2.75 oz instead of 2.0 oz.

    Product
    Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters, 20%, 0.5%, Net WT 2.75 oz (78g); Distributed by Moberg Pharma North America LLC, Cedar Knolls, NJ 07927; UPC 8 51409 00722 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·050-2019·2019-05-07

    Santa Fe Importers Recalls Chicken Meatballs for Undeclared Soy Allergen

    Santa Fe Importers is recalling ready-to-eat chicken meatballs because they contain soy, an undeclared allergen. No adverse reactions have been reported.

    Product
    Santa Fe Importers, Inc. — Santa Fe Importers, Inc. Recalls Ready-To-Eat Chicken Products due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·049-2019·2019-05-04

    Conagra Recalls P.F. Chang's Chicken Entrees for Undeclared Milk Allergen

    Conagra Brands is recalling P.F. Chang's Home Menu Chicken Pad Thai and Chicken Fried Rice products because they contain undeclared milk, a known allergen.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — Conagra Brands, Inc. Recalls Chicken Pad Thai and Chicken Fried Rice Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1307-2019·2019-05-01

    Gianni's Fine Food Recalls Blue Cheese Vinaigrette for Undeclared Milk

    Gianni's Fine Food is recalling 17 bottles of blue cheese vinaigrette because the label failed to declare milk, a major allergen.

    Product
    Blue cheese & toasted walnut garlic balsamic vinaigrette, packaged in 6.3-fl. oz. glass bottle. The label is read in parts: "***Ingredients: balsamic vinegar, extra virgin olive oil, roasted walnuts, blue cheese crumbles, salt, pepper***giannisfinefoods.com***".
    Category
    Food
    Distribution
    2 states
  • HighCPSC·19113·2019-05-01

    DAVIDsTEA Recalls Valentine's Day Stackable Mugs Due to Fire Hazard

    DAVIDsTEA is recalling about 700 Valentine's Day stackable mugs because they were mislabeled as microwave safe, posing a fire hazard if used in a microwave.

    Product
    Valentine's Day stackable mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1303-2019·2019-05-01

    Monarch Southern Barbecue Sauce Recalled for Missing Allergen Information

    The CF Sauer Company is recalling Monarch Southern Barbecue Sauce because the labels failed to declare soy and wheat allergens.

    Product
    MONARCH SOUTHERN BARBECUE SAUCE MADE WITH MUSTARD NET 128 FL OZ(1 GAL) 3.78L INGREDIENTS: WATER, HIGH FRUTOSE CORN SRYUP, SUGAR, TOMATO PASTE, DISTILLED AND CIDER VINEGAR, SALT ***DISTRIBUTED BY/DISTRIBUIDO POR US FOODS, INC., ROSEMOUNT, IL 60015 UPC 7 58108 60016 4
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1298-2019·2019-05-01

    Patagonia Provisions Chipotle Lime Savory Seeds Recalled for Gluten Contamination

    Patagonia Provisions is recalling Chipotle Lime Savory Seeds labeled as gluten-free because they contain gluten in excess of 20 ppm.

    Product
    Patagonia Provisions Chipotle Lime Savory Seeds; 1 oz. poly-film pouches. 12 pouches per case Vegan, Gluten Free Distributed by Patagonia Provisions, Inc. Sausalito, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1299-2019·2019-05-01

    Patagonia Provisions Savory Seeds Recalled for Gluten Contamination

    Patagonia Provisions is recalling Savory Seeds Variety Packs labeled gluten-free because they contain gluten in excess of 20 ppm.

    Product
    Patagonia Provisions Savory Seeds Variety Pack; Classic Barbecue, Chipolte Lime, Mellow Curry 1 oz. poly-film pouches, 12 packages per case Vegan, Gluten Free Distributed by Patagonia Provisions, Inc. Sausalito, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1297-2019·2019-05-01

    Patagonia Provisions Mellow Curry Savory Seeds Recalled for Gluten

    Patagonia Provisions is recalling Mellow Curry Savory Seeds labeled gluten-free because they contain gluten in excess of 20 ppm.

    Product
    Patagonia Provisions Mellow Curry Savory Seeds; 1 oz. poly-film pouches. 12 pouches per case Vegan, Gluten Free Distributed by Patagonia Provisions, Inc. Sausalito, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1296-2019·2019-05-01

    Patagonia Provisions Classic Barbecue Savory Seeds Recalled for Gluten Contamination

    Patagonia Provisions is recalling Classic Barbecue Savory Seeds labeled gluten-free because they contain gluten in excess of 20 ppm.

    Product
    Patagonia Provisions Classic Barbecue Savory Seeds; 1 oz. poly-film pouches. 12 units per case Vegan, Gluten Free Distributed by Patagonia Provisions, Inc. Sausalito, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1212-2019·2019-05-01

    Covidien Endo Grasp Auto Suture Grasper Recalled for Sterilization Labeling Error

    COVIDIEN LLC is recalling 240 units of the Endo Grasp Auto Suture Grasper 5mm because the sterilization method used was not consistent with the labeling and approved method.

    Product
    Covidien Endo Grasp Auto Suture Grasper 5mm REF: 173030 The Covidien Endo Grasp" Auto Suture" grasper 5 mm instrument has applications in a variety of gynecologic, general, urologic, thoracic and endoscopic procedures for temporary grasping/clamping of tissue and small tubula
    Category
    Medical Device
    Distribution
    Distributed nationwide