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.

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.

5176–5200 of 9610

  • LowFDA (Devices)·Z-0596-2017·2016-11-23

    Philips CT Scanner Recall for Incorrect Product Label Rating

    Philips is recalling 15 Ingenuity Core 128 CT scanners because the product labels do not include the correct current rating.

    Product
    Ingenuity Core 128 Computed Tomography X-ray system, Model 728323
    Category
    Medical Device
    Distribution
    15 states
  • LowFDA (Devices)·Z-0595-2017·2016-11-23

    Philips Ingenuity CT System Recalled for Incorrect Label Rating

    Philips is recalling 27 Ingenuity CT systems because the product labels do not include the correct current rating.

    Product
    Ingenuity CT Computed Tomography X-ray system, Model 728326
    Category
    Medical Device
    Distribution
    15 states
  • HighUSDA FSIS·112-2016·2016-11-22

    Omni Custom Meats Recalls Roasted Chicken Quarters Due to Undeclared Soy Allergen

    Omni Custom Meats is recalling approximately 191,695 pounds of marinated Roasted Chicken Quarters because the product contains soy, an undeclared allergen.

    Product
    Omni Custom Meats, Inc. — Omni Custom Meats, Inc Recalls Roasted Chicken Quarters Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighUSDA FSIS·108-2016·2016-11-17

    Pork Barbeque Products Recalled for Undeclared Soy Allergen

    Morty Pride Meats, Inc. is recalling about 237,891 pounds of pork barbeque products because the labels do not declare soy, an allergen present in the Worcestershire sauce used to make them. The products were sold in North Carolina and South Carolina.

    Product
    Morty Pride Meats, Inc. — Morty Pride Meats, Inc. Recalls Pork Barbeque Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0420-2017·2016-11-16

    Brownwood Farms Cherry Raspberry Preserves Recalled for Undeclared Milk

    Brownwood Farms is recalling Cherry Raspberry Preserves because the product contains milk that is not declared on the label.

    Product
    Brownwood Farms Cherry Raspberry Preserves 12oz glass bottles and 1 gallon.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0384-2017·2016-11-16

    Kar Nut Almond Cartons Recalled for Undeclared Walnut Allergen

    Kar Nut Products is recalling Fit & Active 100 Calorie Whole Almonds because walnuts are undeclared on the outer carton.

    Product
    Fit & Active 100 Calorie Whole Almonds 7  0.63oz bags per retail carton Flexible film bags in paperboard carton
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0424-2017·2016-11-16

    Brownwood Farms Strawberry Preserves Recalled for Undeclared Milk

    Brownwood Farms is recalling Strawberry Preserves because the product contains milk that is not declared on the label.

    Product
    Brownwood Farms Strawberry Preserves 12oz glass bottles and 1 gallon. Private labels: Art's Tavern (Strawberry Preserves 12oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0312-2017·2016-11-16

    Trader Joe's Chocolate Sticks Recalled for Undeclared Milk Allergen

    Trader Joe's is recalling Chocolate Orange and Chocolate Raspberry Sticks because they may contain more than the stated traces of milk.

    Product
    Trader Joe's Chocolate Orange Sticks, Net Wt. 18 oz (1lb 2oz) 510g, 36 units per case, UPC 00847162
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0422-2017·2016-11-16

    Brownwood Farms Jalapeno Cherry Butter Recalled for Undeclared Milk

    Brownwood Farms is recalling Jalapeno Cherry Butter products because they contain milk that is not declared on the label.

    Product
    Brownwood Farms Jalapeno Cherry Butter 12oz and 20oz glass bottles and 1 gallon. Private labels: Kimmel Orchard & Vineyard (Jalapeno Cherry Butter 12oz). Benjamin Twiggs (Cherry Pepper Jam 10oz). Central Market (16oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0421-2017·2016-11-16

    Brownwood Farms Pear Preserves Recalled for Undeclared Milk Allergen

    Brownwood Farms is recalling Pear & Cinnamon Preserves because the product contains milk that is not declared on the label.

    Product
    Brownwood Farms Pear & Cinnamon Preserves 10oz glass bottles and 1 gallon.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0313-2017·2016-11-16

    Trader Joe's Chocolate Sticks Recalled for Undeclared Milk Allergen

    Trader Joe's is recalling Chocolate Orange and Chocolate Raspberry Sticks because they may contain more than the stated traces of milk.

    Product
    Trader Joe's Chocolate Raspberry Sticks, Net Wt. 18 oz (1lb 2oz) 510g, 36 units per case, UPC 00847122
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0425-2017·2016-11-16

    Brownwood Farms Cherry Preserves Recalled for Undeclared Milk

    Brownwood Farms is recalling Michigan Cherry Preserves because they contain milk that is not declared on the label.

    Product
    Brownwood Farms Michigan Cherry Preserves 12oz glass bottles and 1 gallon. Private labels: Art's Tavern (Cherry Preserves 12oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0363-2017·2016-11-16

    C.R. Bard Recalls X-Force Nephrostomy Balloon Dilation Catheter Kits

    C.R. Bard is recalling 192 units of X-Force Nephrostomy Balloon Dilation Catheter Kits because a contract manufacturer packaged an incorrect 30Fr sheath instead of the labeled 24Fr sheath.

    Product
    X-Force Nephrostomy Balloon Dilation Catheter Kit with Inflation Device, PTFE Sheath, 8 mm x 15 cm, Product Code 996081 The product is a dual lumen catheter with a 24 (8mm) or 30Fr (10mm) balloon mounted on the distal tip. It has a radiopaque tip and radiopaque marker beneath
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0366-2017·2016-11-16

    FDA Recalls Custom Packaging for Devon Light Gloves

    The FDA is recalling custom packaging for Devon Light Gloves due to added instructions for use regarding barrier integrity inspection.

    Product
    Professional Hospital Supply, Inc Custom Packaging containing the Devon Light Glove Item Number Description 380789003 SURE SET SINGLE BASIN PACK 400383006 MAJOR BASIN PACK 40038300
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0388-2017·2016-11-16

    Akita Sumitomo Bakelite Recalls Mislabeled Sterile Electrosurgical Knives

    Akita Sumitomo Bakelite Co., Ltd. is recalling 15 units of sterile electrosurgical knives that were mislabeled as Standard type instead of Jr type-Long.

    Product
    SB Knife -Electrosurgical Knife, Sterile Size: Working Length 2.3M Maximum OD 2.6mm. Product Usage: The SB Knife is a single-use sterile Electrosurgical Knife (Model Numbers: MD-47703W, MD-47704, MD-47706 and MD-47703L). This device is designed to be used with Olympus and
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0355-2017·2016-11-16

    Island Biscuit Strawberry Snacks Recalled for Undeclared Food Dyes

    Lee'S Food Corp is recalling Island Biscuit "Yum Yum - Creamy Strawberry" snacks because sampling revealed undeclared food dyes.

    Product
    Island Biscuit "Yum Yum - Creamy Strawberry" Biscuit Snack, Net Wt. 30 g, UPC 4 800098 122952
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0389-2017·2016-11-16

    Sumitomo Bakelite Electrosurgical Knives Recalled for Mislabeled Sterilization Pouches

    Akita Sumitomo Bakelite Co., Ltd. is recalling 8 units of electrosurgical knives because their sterilization pouches and cartons were mislabeled as Standard Type instead of Short type.

    Product
    SB (Sumitomo Bakelite Co.,) Electrosurgical Knife Size: Working Length 1.8M Maximum OD 2.6mm. Product Usage: The SB Knife is a single-use sterile Electrosurgical Knife (Model Numbers: MD-47703W, MD-47704, MD-47706 and MD-47703L). This device is designed to be used with Oly
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0380-2017·2016-11-16

    Stryker Recalls Reprocessed Diagnostic Electrophysiology Catheters Due to Mislabeled French Size

    Stryker Sustainability Solutions is recalling four reprocessed Daig Steerable and Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters because they may be mislabeled for French size during reprocessing.

    Product
    Reprocessed Daig Steerable and Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters Model Numbers: 401940, 402004 UPC Code: 00885825007409 00885825007744 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit e
    Category
    Medical Device
    Distribution
    3 states
  • LowFDA (Food)·F-0324-2017·2016-11-16

    Tasty Toppings Recalls Dorothy Lynch Homestyle Condiment Bottles

    Tasty Toppings Inc is recalling Dorothy Lynch Homestyle condiment bottles due to a Class III FDA recall. Consumers should return affected products to the store for a refund.

    Product
    Dorothy Lynch Homestyle 8 oz., 16 oz., and 32 oz. bottles (12/case) and 128 oz. bottles (4/case)
    Category
    Food
    Distribution
    12 states
  • HighUSDA FSIS·107-2016·2016-11-15

    Piccadilly Fine Foods Recalls Beef Shepherd's Pie for Undeclared Fish Allergen

    Piccadilly Fine Foods is recalling approximately 144 pounds of beef shepherd's pie due to misbranding and undeclared anchovies (fish) in the Worcestershire sauce.

    Product
    Piccadilly Fine Foods Recalls Beef Shepherd’s Pie Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·102-2016 EXP·2016-11-09

    Flavor Trade Recalls Beef Jerky Produced Without Federal Inspection

    Flavor Trade, LLC. is recalling 741 pounds of beef jerky produced without federal inspection and shipped to Kansas and Missouri.

    Product
    Flavor Trade, LLC. Recalls Beef Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0374-2017·2016-11-09

    Whole Foods Asparagus Pea Salad Recalled for Undeclared Eggs

    Whole Foods Market is recalling Asparagus Pea & Ricotta Salad because it contains undeclared eggs. The product was sold in five northeastern states.

    Product
    Whole Foods Asparagus Pea & Ricotta Salad, 10 Ounces
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0369-2017·2016-11-09

    Roland Preserved Lemons Recalled for Undeclared Sulfites

    Roland Foods is recalling preserved lemons because testing found undeclared sulfites. Consumers should check their jars for specific lot numbers.

    Product
    Roland¿ Preserved Lemons, NET WT. 12.35 OZ., and Roland¿ PRESERVED LEMONS - BELDI, NET WT. 13 OZ., Item UPC 4122461002 and Case UPC 10041224610023 -- PACKED EXCLUSIVELY FOR ROLAND FOODS LLC, NEW YORK, NY 10010 --- The product is packed in a glass jar.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0327-2017·2016-11-09

    B. Braun Recalls Spinal Anesthesia Trays with Lidocaine Component

    B. Braun Medical is voluntarily recalling specific lots of Custom Spinal Anesthesia Trays because the lidocaine component does not meet color specifications.

    Product
    Affected Pain Control Tray Component (5% Lidocaine Hydrochloride and 7.5% DExtrose Injection, USP) Injection of anesthetics to provide regional anesthesia
    Category
    Medical Device
    Distribution
    6 states