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.

2551–2575 of 9607

  • LowFDA (Devices)·Z-2555-2019·2019-10-02

    Arrow International Recalls Central Venous Access Kits Due to Incorrect Banner Card

    Arrow International Inc is recalling 520 units of ARROW+gard Blue PSI Kit Cath-Gard central venous access devices because they may contain the incorrect banner card.

    Product
    8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard for use with 7.5 - 8 Fr.Catheters Product Code: CDC-29803-1A - Product Usage: The MACTM Two-Lumen Central Venous Access Device with ARROWg+ard Blue¿ permits venous access and catheter introduction to the central circulation. It m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2557-2019·2019-10-02

    Randox Urinalysis Control Level 2 Recalled for Incorrect Leukocyte Range

    Randox Laboratories is recalling Randox Urinalysis Control Level 2 kits because the leukocyte range for the Siemens Multistix method was incorrect.

    Product
    Randox Urinalysis Control Level 2 (IVD) Ref: UC5034 - Product Usage: Product is intended for in vitro diagnostic use in the quality control of urine test strips.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V682000·2019-09-27

    Jaguar Recalls 2019-2020 F-Type Vehicles for Incorrect Tire Placard Label

    Jaguar is recalling 2019-2020 F-Type vehicles with 18-inch rear wheels because the tire placard label lists an incorrect tire size, which could lead to improper tire installation.

    Product
    JAGUAR — JAGUAR F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·19V694000·2019-09-26

    Honda Recalls 2019 CR-V for Incorrect Airbag Owner's Guide Information

    Honda is recalling 2019 CR-V vehicles because the owner's guide incorrectly describes the Passenger Airbag Off indicator, potentially increasing injury risk in a crash.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2545-2019·2019-09-25

    CooperSurgical Recalls LEEP Return Patient Pads Due to Expiration Date Errors

    CooperSurgical is recalling LEEP Return Patient Pads because the expiration dates on the outer boxes have the month and day reversed compared to the individual pouches.

    Product
    LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0006-2020·2019-09-18

    QQ Fish Seafood Balls Recalled for Undeclared Egg Allergen

    Great One Trading Inc. is recalling QQ Fish brand Shrimp Flavoured Seafood Balls because they contain an undeclared egg allergen.

    Product
    QQ Fish brand SHRIMP FLAVOURED SEAFOOD BALL; Net weight 200g/7oz
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0007-2020·2019-09-18

    QQ Fish Cuttlefish Flavored Seafood Balls Recalled for Undeclared Egg

    Great One Trading Inc. is recalling QQ Fish brand Cuttlefish Flavored Seafood Balls because the product contains an undeclared allergen, specifically egg.

    Product
    QQ Fish brand CUTTLEFISH FLAVOURED SEAFOOD BALL; Net weight 200g/7oz
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2246-2019·2019-09-18

    YoCrunch Vanilla Yogurt Recalled for Undeclared Peanuts and Eggs

    Danone Waters of America is recalling YoCrunch Vanilla Lowfat Yogurt with Snickers Pieces due to an incorrect overwrap that results in undeclared peanuts and eggs.

    Product
    YoCrunch VANILLA LOWFAT YOGURT WITH SNICKERS PIECES 4 - 4 oz (113g) - 16 oz (453g) 6 packaged or 4 cups per case. UPC 46675 01326
    Category
    Food
    Distribution
    34 states
  • HighFDA (Food)·F-0005-2020·2019-09-18

    QQ Fish Crab Flavored Seafood Ball Recalled for Undeclared Egg

    Great One Trading Inc. is recalling QQ Fish brand Crab Flavored Seafood Ball because it contains undeclared egg, a major allergen not listed on the label.

    Product
    QQ Fish brand CRAB FLAVOURED SEAFOOD BALL; Net weight 200g/7oz
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2149-2019·2019-09-18

    Bakkavor USA Recalls Savory Tuna Salad Due to Undeclared Shrimp

    Bakkavor USA is recalling 16-ounce Savory Tuna Salad containers distributed in Texas because the product contains undeclared shrimp.

    Product
    Savory Tuna salad 16 oz. packaged in Clear PP containers UPC 4122033749
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2154-2019·2019-09-18

    Cena Vegan Pollo Asado Recalled for Undeclared Soy Allergen

    Cena Vegan is recalling Pollo Asado plant-based meat because an inspection found undeclared hydrolyzed soy protein, a major allergen.

    Product
    Cena Vegan Pollo Asado Plant-Based Meat; Net Wt. 16 oz. (448 grams) retail, Net Wt. 5 lb. - food service; UPC: 8 55687 00701 5; Ingredient: Vital wheat gluten, Garbanzo bean flour, Vegetable bouillon, Orange juice, Less than 2% of: Vegetable Oil, Lime Juice, Onion Powder,
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2121-2019·2019-09-18

    Martha White Gluten Free Cornbread Mix Recalled for Gluten Presence

    Hometown Food Company is recalling Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix because the product tested positive for gluten despite being labeled gluten-free.

    Product
    Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix packaged in a 7oz. pouch. 12 pouches per wholesale case. Item UPC: 0 1330082014 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2538-2019·2019-09-18

    Smith & Nephew Recalls Legion Hemi Step Tibial Wedge Due to Packaging Error

    Smith & Nephew is recalling 12 units of Legion Hemi Step Tibial Wedges because they were inadvertently packaged with an incorrect screw component.

    Product
    LEGION(TM) HEMI STEP TIBIAL WEDGE RK/HK, 5 MM, SIZE 3-4 LT.MDL/RT-LAT, REF 71423432 Product Usage: The constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-2152-2019·2019-09-18

    Stonyfield Kids Strawberry Beet Berry Tubes Recalled for Misbranding

    Stonyfield Farm is recalling 4,064 cartons of Kids Strawberry Beet Berry Tubes because the outer carton labeling does not match the product.

    Product
    Stonyfield Kids Strawberry Beet Berry Tubes, 8 count-2oz each; 453g/package; Keep Refrigerated
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-2144-2019·2019-09-18

    Calcium Supplement Recalled for Lacking Declared Vitamin D Content

    Jivan Shakti Inc. is recalling 790 bottles of Dr. Naram's Rasayana D Tablet because FDA testing found no Vitamin D in the product.

    Product
    Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C., DR. NARAM'S RASAYANA D TABLET, Calcium Supplement with Vitamin D*, Dietary Supplement, 60 Tablets, FOR EXPORT ONLY, Imported & Distributed by: Jivan Shakti INC, 933 South Street, Peekskill, NY 10566, Manufactur
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Food)·F-2151-2019·2019-09-18

    FungusAmongUs Shiitake Organic Mushrooms Recalled for Undeclared Sulfites

    Seattle Gourmet Foods Inc. is recalling FungusAmongUs Shiitake Organic Mushrooms due to undeclared sulfites detected by the Florida Department of Agriculture.

    Product
    FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a clear cellophane bag, net Weight 1 ounce. UPC 7 19870 60023 3 for individual 1 ounce bags UPC 50719870600016 for Master caddy that holds 8 packages of 1 ounce bags The label is read in parts: "***O
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2153-2019·2019-09-18

    Abbott Recalls Similac Pro-Sensitive Bottles Due to Packaging Error

    Abbott Nutrition is recalling specific cartons of Similac Pro-Sensitive that may contain Similac Pro-Advance bottles due to a packaging error.

    Product
    Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
    Category
    Food
    Distribution
    8 states
  • LowFDA (Drugs)·D-1847-2019·2019-09-18

    Lamivudine Tablets Recalled for Incorrect Package Insert Labeling

    American Health Packaging is recalling Lamivudine Tablets due to an error in the package insert that incorrectly lists tablet description coding.

    Product
    Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton, NDC 60687-362-21 (Individual Dose NDC: 60687-362-11), Distributed by American Health Packaging, Columbus, OH
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2490-2019·2019-09-18

    Randox Calibration Serum Recalled for Incorrect Analyte Targets

    Randox Laboratories is recalling calibration sera due to realigned targets for AST and ALT. The recall affects 307 kits distributed nationwide and in several foreign locations.

    Product
    This is an in vitro diagnostic product intended for use as a calibration serum in clinical chemistry assays. Randox calibration sera contain 42 analytes and are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·092-2019·2019-09-17

    Perdue Recalls Frozen Chicken Tenders for Undeclared Wheat Allergen

    Perdue Foods is recalling approximately 495 pounds of frozen chicken breast tenders because they contain undeclared wheat and are mislabeled as gluten-free.

    Product
    Perdue Foods LLC — Perdue Foods LLC Recalls Simply Smart Organics Frozen Chicken Ready-to-Eat Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2355-2019·2019-09-11

    Norm-O-Temp 111Z Medical Device Recalled for Missing Tissue Damage Warning

    Cincinnati Sub-Zero Products LLC is recalling Norm-O-Temp model 111Z devices because the manual lacks instructions warning that exceeding 40 Celsius for extended periods can cause tissue damage.

    Product
    Norm-O-Temp model 111Z
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Food)·F-2106-2019·2019-09-11

    Vitony Bakery Guava-Coconut Pudding Cake Recalled for Undeclared Sulfite

    Vitony Bakery is recalling 1,041 units of Guava-Coconut Pudding Cake because the product fails to declare sodium metabisulfite on the label.

    Product
    Vitony Bakery, Bizcocho de Guayaba y Coco (Guava-Coconut Pudding Cake); Peso Neto 14 ONZ. (397 G)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2104-2019·2019-09-11

    Vitony Bakery Guava Cheese Cake Roll Recalled for Allergen Mislabeling

    Vitony Bakery is recalling Guava Cheese Cake Rolls because the packaging failed to declare soy and specific food dyes, and lacked refrigeration instructions.

    Product
    Vitony Bakery, Brazo Gitano Guayaba Queso (Guava- Cheese Cake Roll); Peso Neto 12 ONZ. (340 G)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2356-2019·2019-09-11

    Norm-O-Temp 111W Medical Device Recalled for Missing Tissue Damage Warning

    Cincinnati Sub-Zero Products LLC is recalling Norm-O-Temp model 111W units because the manual lacks instructions warning that exceeding 40 Celsius for extended periods can cause tissue damage.

    Product
    Norm-O-Temp model 111W
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-2442-2019·2019-09-11

    Boston Scientific Recalls Mislabeled AMS 800 Artificial Urinary Sphincter Cuffs

    Boston Scientific is recalling AMS 800 Artificial Urinary Sphincter belt cuffs labeled as 4.5 cm but measuring 4.0 cm due to mislabeling.

    Product
    AMS 800 Artificial Urinary Sphincter AMS 800 Belt Cuff, 4.5 cm Part Number: 72400161
    Category
    Medical Device
    Distribution
    1 state