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.

1651–1675 of 9607

  • ModerateFDA (Food)·F-0182-2021·2020-12-30

    Canyon Bakehouse Gluten-Free Bagels Recalled for High Gluten Levels

    Flowers Foods is recalling Canyon Bakehouse Gluten-Free Bagels because some products contained higher than acceptable levels of gluten.

    Product
    CANYON BAKEHOUSE GLUTEN FREE BAGELS EVERYTHING NET WT. 14 OZ (396g) Canyon Bakehouse, LLC Johnstown, CO 80534 UPC 8 53584 00221 8
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-0638-2021·2020-12-30

    Biocomposites Recalls Stimulan Kit 10cc Due to Mislabeled Product

    Biocomposites, Ltd. is recalling 54 boxes of Stimulan Kit 10cc, Model 600-010, because the product is mislabeled. The recall affects units distributed in the US, Puerto Rico, and Costa Rica.

    Product
    Stimulan Kit 10cc, Model 600-010 - Product Usage: intended for use as a bone void filler for voids or gaps that are not intrinsic to the stability of the bony structure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0725-2021·2020-12-30

    Integra Recalls Mislabeled Bactiseal Endoscopic Ventricular Catheters

    Integra LifeSciences is recalling 17 Bactiseal Endoscopic Ventricular Catheters due to mislabeling. The devices were incorrectly identified as a different catheter model.

    Product
    Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use in the treatment of hydrocephalus when shunting cerebrospinal fluid (CSF) from the ventricles of the brain. Part Number: 823087
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0698-2021·2020-12-30

    AMT ENFit-to-Stepped Male Adapter Recalled for Incorrect Pouch Labels

    Applied Medical Technology Inc is recalling specific lots of ENFit-to-Stepped Male adapters because the inner pouches may have incorrect labels, although the outer boxes are correct.

    Product
    AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102. Box PN TRN102, Box UDI (01)00842071109066(17)230901(10)200918-103, Pouch PN ETRN102, Pouch UDI (01)00842071108007(17)230901(10)200902-075
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0172-2021·2020-12-23

    Holiday Cookie Platter Recalled for Undeclared Pecans

    George DeLallo Co. is recalling Holiday Cookie Platters due to undeclared pecans, a major food allergen.

    Product
    Holiday Cookie Platter packaged in plastic container 20 OZ (1.25 LB) 567g. UPC 41415 88690
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0189-2021·2020-12-23

    Treehouse Foods Recalls Honey Mustard Dressing for Unlabeled Milk

    Treehouse Foods is recalling House Recipe Honey Mustard Dressing & Dip because it contains milk, which is not listed on the label.

    Product
    HOUSE RECIPE HONEY MUSTARD DRESSING & DIP NET WT 1 OZ.(28g) cup CONTAINS: EGGS DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077 UPC 0 73473 05797 8
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0171-2021·2020-12-23

    Market of Choice Recalls Sour Cherry Baked Brie for Almond Mislabeling

    Market of Choice Inc. is recalling Sour Cherry Baked Brie because the scale label failed to list almond as an ingredient.

    Product
    Market of Choice brand Sour Cherry Baked Brie is wrapped in a plastic shrink wrap and has a white adhesive store label. UPC 0 217241 414996. The label is read in parts: "***SOUR CHERRY BAKED BRIE*** Puff Pastry (wheat flour, niacin, reduced iron, thiamine mononitrate, riboflav
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0180-2021·2020-12-23

    Fusion Health Recalls Pharmorigins Core Supplement for Unapproved Additive

    Fusion Health and Vitality LLC is recalling Pharmorigins Core dietary supplements due to the unapproved use of a food additive and unapproved marketing statements.

    Product
    PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g) Supplement Facts***Hordenine HCL*** Manufactured by: Fusion Health Vitality, LLC 1360 Union Hill Road, Suite 11B Alpharetta, GA 30004 888.964.5327 UPC 7 28028 21054
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0570-2021·2020-12-23

    Zimmer Biomet Recalls Polaris Spinal System Screws for Labeling Update

    Zimmer Biomet is updating instructions for Polaris and Cypher spinal screws to warn against using them with direct current stimulation due to construct failure risks.

    Product
    Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·PHA-12192020-01·2020-12-19

    USDA Issues Public Health Alert for Ineligible Imported Frozen Chicken Wings

    USDA FSIS issued a public health alert for raw frozen chicken wings from China labeled with a false USDA mark. No recall was requested as the product is no longer in commerce.

    Product
    FSIS Issues Public Health Alert for Ineligible Imported Raw Frozen New Orleans - Roasted Chicken Wings from the Peoples Republic of China
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0168-2021·2020-12-16

    Whole Foods Market Recalls Popcorn Chicken Shaker with Sweet Chili

    Whole Foods Market is recalling Popcorn Chicken Shaker with Sweet Chili due to undeclared shrimp allergen.

    Product
    Whole Foods Market Popcorn Chicken Shaker with Sweet Chili Variable weight sold by lb. Packed For Whole Foods Market
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0161-2021·2020-12-16

    Prairie Farms Chocolate Milk Recalled for Undeclared Egg

    Prairie Farms is recalling 355 gallons of chocolate milk sold in the Chicago area due to undeclared egg.

    Product
    Prairie Farms Premium Flavored Chocolate Milk, 1 gallon, UPC 72730-26110
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0159-2021·2020-12-16

    Chef Myron's Premium Shoyu Sauce Recalled for Gluten-Free Mislabeling

    JMH International is recalling Chef Myron's Premium Shoyu Sauce because it contains wheat-derived gluten despite a gluten-free claim.

    Product
    Chef Myron's Premium Shoyu Sauce, 1 GAL (3.78 L), Item # 400023077, 2 bottles/case; 5 GAL (18.92 L), Item # 400023279, plastic pail
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0154-2021·2020-12-16

    Chef Myron's Teriyaki Sauce Recalled for Gluten-Free Mislabeling

    JMH International is recalling Chef Myron's Premium Teriyaki Sauce because it contains wheat-derived gluten despite a gluten-free claim.

    Product
    Chef Myron's Premium Teriyaki Sauce, 64 FL OZ (1.89 L), Item # 400023118, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0537-2021·2020-12-16

    Chromsystems MassChrom Amino Acid Analysis Plasma Control Level I Recalled

    Chromsystems Instruments & Chemicals GmbH is recalling MassChrom Amino Acid Analysis Plasma Control Level I kits because they do not meet stability criteria and may impact results.

    Product
    MassChrom Amino Acid Analysis Plasma Control Level I, Order No. 0471 - Product Usage: The kit is intended for amino acid metabolic screening, confirmation of a tentative diagnosis, and monitoring of treatment in individuals diagnosed with a metabolic disorder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0539-2021·2020-12-16

    Chromsystems Recalls MassChrom Amino Acid Analysis Plasma Control Level III

    Chromsystems Instruments & Chemicals GmbH is voluntarily recalling 342 vials of MassChrom Amino Acid Analysis Plasma Control Level III due to a Class II device defect.

    Product
    MassChrom Amino Acid Analysis Plasma Control Level III, Order No. 0473 - Product Usage: The kit is intended for amino acid metabolic screening, confirmation of a tentative diagnosis, and monitoring of treatment in individuals diagnosed with a metabolic disorder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0155-2021·2020-12-16

    Chef Myron's Szechuan Sauce Recalled for Gluten-Free Mislabeling

    JMH International is recalling Chef Myron's Szechuan Sauce because it contains wheat-derived fermented soy sauce despite a gluten-free claim.

    Product
    Chef Myron's Szechuan Sauce, 64 FL OZ (1.89 L), Item # 400023293, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0157-2021·2020-12-16

    Chef Myron's Tsukeyaki Sauce Recalled for Gluten-Free Labeling Error

    JMH International is recalling Chef Myron's Tsukeyaki Sauce because it contains wheat-derived ingredients despite a gluten-free claim.

    Product
    Chef Myron's Tsukeyaki Sauce, 64 FL OZ (1.89 L), Item # 400023276, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0563-2021·2020-12-16

    Spacelabs Sentinel V10 and V11 Software Upgrade Recall

    Spacelabs Healthcare is recalling Sentinel V10.x and V11.x software because system upgrades may add or overwrite unrelated comments on existing ECG and ABP tests.

    Product
    Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is easy to install and to use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0548-2021·2020-12-16

    Integra Recalls Mayfield A2000 Skull Cap Instruction Manual

    Integra LifeSciences Corp. is recalling 552 instruction manuals for the Mayfield A2000 Skull Cap to correct inaccurate illustrations.

    Product
    Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: intended for or rigid skeletal fixation during neurosurgical procedures. P/N: 451A2000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0535-2021·2020-12-16

    LivaNova Recalls VNS Therapy SENTIVA DUO Generators Due to Model Number Error

    LivaNova is recalling eight SENTIVA DUO VNS Therapy generators because they display the incorrect model number after a device reset.

    Product
    VNS Therapy SENTIVA DUO # 1000-D - Product Usage: indicated for the treatment of chronic or recurrent depression in patients who are experiencing a treatment-resistant or treatment- intolerant depressive episode.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0152-2021·2020-12-16

    Chef Myron's Eurasian Fusion Sauce Recalled for Gluten Mislabeling

    JMH International is recalling Chef Myron's Eurasian Fusion Sauce because it contains wheat-derived fermented soy sauce despite a gluten-free claim.

    Product
    Chef Myron's Eurasian Fusion Sauce, 64 FL OZ (1.89 L), Item # 400023288, 4 bottles/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0153-2021·2020-12-16

    Chef Myron's Ponzu Sauce Recalled for Gluten-Free Labeling Error

    JMH International is recalling Chef Myron's Ponzu Sauce because it contains wheat-derived ingredients despite a gluten-free claim.

    Product
    Chef Myron's Ponzu Sauce, 64 FL OZ (1.89 L), Item # 400023110, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide