The Recall Desk

Hazard

Mis Labeling recalls

9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,622
Critical
163
Severe
590
Most recent
2026-09-24

Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (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.

9501–9525 of 9622

  • ModerateFDA (Food)·F-1636-2012·2012-07-04

    Young Ocean Recalls Salted Pollock Roe Due to Undeclared Artificial Colors

    Young Ocean, Inc. is recalling approximately 1,920 pounds of salted pollock roe sold in Washington due to the use of undeclared artificial colors Red #5, Yellow #5, and Red #40.

    Product
    Salted/marinated Pollock roe packaged in white plastic trays with either a clear or opaque plastic lid. Product is packaged in 1.0 lb., 2.2 lb., and 5 lb. sizes and is labeled in part: "Marinated Pollock Roe***Weight: 5.0lb***Production Date: March 2012 Packed by: Young Ocean In
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1661-2012·2012-07-04

    Mexicantown Wholesale Recalls Concha Rosa for Undeclared Yellow Dye

    Mexicantown Wholesale is voluntarily recalling Concha Rosa products distributed in Michigan due to the presence of undeclared FD&C Yellow #6.

    Product
    CONCHA ROSA QTY: 90 MEXICANTOWN BAKERY 313-894-2000
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1466-2012·2012-06-27

    Santos Deggi Mirch Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling Deggi Mirch spice products because they were packaged on shared equipment with peanuts and wheat, posing an allergen risk.

    Product
    Santos Brand, Deggi Mirch (Red Capsicum & Kashmiri Red Chile Powder) packed in clear plastic bags, 7 ounces, 14 ounces, 2 pounds
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1471-2012·2012-06-27

    Santos Mustard Seeds Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling mustard seeds due to cross-contact with peanuts and wheat on shared equipment, which were not declared on the packaging.

    Product
    Santos Brand, Mustard Seeds packed in clear plastic bags, 3.5 ounces, 16 ounces
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1472-2012·2012-06-27

    Santos Brand Urid Split Lentils Recalled for Undeclared Peanuts and Wheat

    Santos Inc. is recalling Urid Split Lentils because they were processed on shared equipment with peanuts and wheat, which are not listed on the packaging.

    Product
    Santos Brand, Urid Split (Lentils) packed in clear plastic bags, 2 pounds, 4 pounds
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1473-2012·2012-06-27

    Santos Brand Suji Flour Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling 2-pound bags of Suji (Farina) because routine inspections found the product was processed on shared equipment with peanuts and wheat, which are not listed on the packaging.

    Product
    Santos Brand, Suji (Farina) packed in clear plastic bags, 2 pounds
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1463-2012·2012-06-27

    Santos Cinnamon Sticks Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling cinnamon sticks because they were packaged on equipment shared with peanuts and wheat, posing an allergen risk.

    Product
    Santos Brand, Cinnamon Sticks packed in clear plastic bags, 7oz, 14oz
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-1386-2012·2012-06-27

    Physicians Total Care Recalls Morphine Sulfate Tablets Due to Labeling Error

    Physicians Total Care is recalling Morphine Sulfate tablets because bottles may be mislabeled, potentially containing the wrong formulation.

    Product
    Morphine Sulfate Immediate Release tablet, 30 mg/120 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, OK 74146-6234, NDC 54868-4973-00
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1474-2012·2012-06-27

    Santos Garbanzo Beans Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling Santos Brand garbanzo beans because they were cross-packaged with peanuts and wheat flour, posing an allergen risk.

    Product
    Santos Brand, garbanzo beans packed in clear plastic bags, 2 pounds, 4 pounds
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1467-2012·2012-06-27

    Santos Garam Masala Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling Garam Masala spice mix because it was packaged on shared equipment with peanuts and wheat, posing an allergen risk.

    Product
    Santos Brand, Garam Masala (Indian Spice Mix) packed in clear plastic bags, 7 ounces, 16 ounces
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1470-2012·2012-06-27

    Santos Brand Whole Mace Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling Santos Brand Whole Mace because it was cross-packaged with peanuts and wheat, posing an allergen risk.

    Product
    Santos Brand, Whole Mace packed in clear plastic bags, 3.5 ounces, 7 ounces
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1465-2012·2012-06-27

    Santos Fennel Seeds Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling fennel seeds due to cross-packaging with peanuts and wheat flour, which were not declared on the packaging.

    Product
    Santos Brand, Fennel Seeds packed in clear plastic bags, 3.5 ounces, 7 ounces, 14 ounces, 2 pounds
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1464-2012·2012-06-27

    Santos Cumin Seeds Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling cumin seeds because routine inspections found they were packaged with peanuts and wheat, posing a risk to allergic consumers.

    Product
    Santos Brand, Cumin Seeds packed in clear plastic bags, 7 ounces, 14 ounces, 2 pounds
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1462-2012·2012-06-27

    Santos Brand Flour Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling All Purpose flour due to cross-contact with peanuts and wheat on shared equipment, which were not listed on the packaging.

    Product
    Santos Brand, All Purpose flour packed in clear plastic bags, 2 lbs, 5lbs
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1468-2012·2012-06-27

    Santos Brand Ginger Powder Recalled for Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling Santos Brand Ginger Powder because it was packaged on shared equipment with peanuts and wheat, posing an allergen risk.

    Product
    Santos Brand, Ginger Powder packed in clear plastic bags, 7 ounces, 14 ounces, 2 pounds
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1469-2012·2012-06-27

    Santos Cardamom Recalled Due to Undeclared Peanut and Wheat Traces

    Santos Inc. is recalling cardamom because it was packaged on shared equipment with peanuts and wheat, which are not listed on the label.

    Product
    Santos Brand, Cardamom packed in clear plastic bags, 3.5 ounces, 7 ounces
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1385-2012·2012-06-27

    Physicians Total Care Recalls Morphine Sulfate Extended Release Tablets Due to Labeling Error

    Physicians Total Care is recalling Morphine Sulfate Extended Release tablets because bottles may be mislabeled as Immediate Release or vice versa.

    Product
    Morphine Sulfate Extended Release tablet, 30 mg, 60 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, Ok 74146-6234, NDC 54868-4033-00
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-1817-2012·2012-06-27

    American Optisurgical Recalls TX1 Tissue Removal System Consoles

    American Optisurgical Inc is recalling five TX1 Tissue Removal System Consoles due to an incorrect pressure relief valve and inaccurate technical specifications.

    Product
    TX1 Tissue Removal System Console. Model: TX1 TX1 Tissue Removal System is an ultrasonic aspirator that emulsifies and removes soft tissue. The TX1 Console provides control over each mode of operation, as well as the user interface via LCD touchscreen and audible tones for confi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1543-2012·2012-06-27

    Oskri Peach Granola Recalled for Unlabeled Cashews

    Oskri Organics Corp. is recalling 1,056 bags of Peach Granola because cashews were added to the product in error, posing a risk to consumers with cashew allergies.

    Product
    Oskri, Peach Granola, Gluten Free, Nut Free, Dairy Free, Vegan, Halal, Kosher, Ingredients: Buck Wheat , Peaches 20% Sunflower Seeds , Apricots, Date Syrup, Chicory Root extract, Rice protein., NET WT 3.5oz (100) G., UPC 66616111743, Oskri, Lake Mills, Wisconsin 53551.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1818-2012·2012-06-27

    Philips Digital Diagnost Software Recall for Image Marker Error

    Philips Healthcare Inc. is recalling Digital Diagnost Software releases 2.0.2 and 2.0.2SP1 because a mirrored image marker can be mistaken for a right-side patient indicator.

    Product
    Philips Digital Diagnost Software, software release 2.0.2 and 2.0.2SP1 including mirror icon Stationary Fluoroscopic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1820-2012·2012-06-27

    NIMS Recalls Exer-Rest Brochures for Unsubstantiated Claims

    Non-Invasive Monitoring Systems, Inc. is voluntarily recalling 91 Exer-Rest marketing brochures nationwide because they contain unsubstantiated health claims.

    Product
    USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device, Models AT3800 and AT4700. Brochure: "EXER-REST***A patented, FDA regist
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1822-2012·2012-06-27

    Ultradent Recalls Peak SE Primer Kits Due to Mislabeled Syringes

    Ultradent is recalling specific Peak SE Primer Kits because a syringe was mislabeled as Peak LC Bond Resin, posing a risk to dental bonding procedures.

    Product
    Peak SE Primer Kits (4 syringes per kit) manufactured by Ultradent Products, Inc, South Jordan, UT, Self Etch Primer. The product is contained within prefilled, labeled syringes in a transparent plastic container identified with an aqua, red, orange, blue and black label with bl
    Category
    Medical Device
    Distribution
    0 states