The Recall Desk

Hazard

Mis Labeling recalls

9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,606
Critical
160
Severe
588
Most recent
2026-09-09

Of the 9,606 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.

526–550 of 9606

  • CriticalFDA (Food)·F-1044-2024·2024-03-13

    Vegetarian Pia Cake Taro Durian Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling Vegetarian Pia Cake Taro Durian (14 oz bags) due to undeclared egg allergen. The recall affects approximately 222,320 bags distributed across 31 U.S. states and Canada.

    Product
    Vegetarian Pia Cake Taro Durian, 14 oz (400g)
    Category
    Food
    Distribution
    32 states
  • HighFDA (Devices)·Z-1253-2024·2024-03-13

    Apollo Onyx Delivery Microcatheter recalled for incorrect indications for use

    Micro Therapeutics is recalling Apollo Onyx Delivery Microcatheter devices with incorrect indications for use. European-version devices were distributed in the U.S. across 29 states.

    Product
    The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the infusion of the Onyx liquid embolic system (LES). The catheter has a semi-rigid proximal shaft and a highly flexible distal shaft to facilitate the advancement of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1250-2024·2024-03-13

    MRI System Spatial Field Gradient Values Incorrectly Displayed and Documented

    Vantage Titan MRI systems display and document spatial field gradient values that are lower than correct, which may cause discomfort in patients with MR-conditional devices.

    Product
    Vantage Titan, Model: MRT-1504
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1249-2024·2024-03-13

    MRI System Displays Incorrect Field Gradient Safety Values

    Canon Medical's Vantage Elan MRI system may display incorrect maximum Spatial Field Gradient values, potentially causing discomfort in patients with MR conditional devices.

    Product
    MRI system: Vantage Elan, Model: MRT-2020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1033-2024·2024-03-13

    Dried Tangerine Plum Recalled Due to Undeclared Sulfites

    Rong Shing Trading NY Inc is recalling 4.7oz bottles of Dried Tangerine Plum due to undeclared sulfites. Products distributed in Florida and New York with best-before date 05/31/2023 may be affected.

    Product
    Dried Tangerine Plum; packaged in 4.7oz (135g) clear plastic bottle; UPC 6928580580214
    Category
    Food
    Distribution
    2 states
  • HighUSDA FSIS·013-2024·2024-03-13

    Kroger Apple Walnut Chicken Salad Bowl Recalled for Undeclared Wheat

    Taylor Farms Pacific is recalling Kroger brand apple walnut with chicken salad bowls due to undeclared wheat allergen. No adverse reactions have been reported.

    Product
    Taylor Farm - Pacific — Taylor Farms Pacific Recalls Kroger Brand Ready-To-Eat Apple Walnut With Chicken Salad Bowl Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    12 states
  • HighNHTSA·24V186000·2024-03-08

    Coachmen Prism Motorhomes Recalled for Incorrect Seat Belt Labeling

    Forest River is recalling 2023-2024 Coachmen Prism motorhomes because the Federal Information label may list the wrong number of seat belts, leading to incorrect cargo capacity information.

    Product
    COACHMEN — COACHMEN PRISM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1219-2024·2024-03-06

    Hip Implant Component Mislabeled With Wrong Insert Type on Packaging

    LINK BiMobile hip implant liners are being recalled because packaging incorrectly identifies the insert type as F instead of G. This labeling error could delay surgery or result in the wrong component being used.

    Product
    LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 184-280/12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1001-2024·2024-03-06

    Reser's Amish Macaroni Salad recalled for undeclared wheat allergen

    Reser's Amish Macaroni Salad is recalled because some containers have a mislabeled side label that does not declare wheat, which is an ingredient in the product. This poses a risk to people with wheat allergies.

    Product
    The recalled Reser's Amish Macaroni Salad was packaged in a plastic clear container where the top lid is labeled as Reser's Amish Macaroni Salad, Net Wt. 1lb., and the container side label indicates Reser s Southern Style with Egg Potato Salad, Net Wt. 1lb. UPC 0 71117 19044 1.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0930-2024·2024-03-06

    Healthprint Vitamin D3 5000 recalled for sub-potency and incorrect labeling

    Ancient Formulas' Healthprint Vitamin D3 5000 supplement contains less Vitamin D than claimed and has incorrect daily value labeling. The recall affects 111 bottles distributed in Florida.

    Product
    Healthprint Vitamin D3 5000 Dietary Supplement, 200 tablets, packaged in plastic bottle.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0908-2024·2024-02-28

    Spice product recalled for undeclared wheat allergen

    Vandevi Compounded Asafoetida spice is recalled due to undeclared wheat. Consumers with wheat allergies should not use this product.

    Product
    Vandevi Compounded Asafoetida 50 gm, 100 gms 200 gm, 500 gm, 1 kg. Packaged in yellow plastic bottles with plastic shrink wrap blue/yellow labels.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1153-2024·2024-02-28

    EndoVive Replacement Button Kits mislabeled with incorrect sizing

    Boston Scientific is recalling EndoVive Replacement Button Kits due to sizing mislabeling that could cause undersizing and serious complications including tissue damage and sepsis.

    Product
    EndoVive Replacement Button Kit w/ ENFIT 28F 2.8 CM, Outer Box UPN M00509500 or M00509510.
    Category
    Medical Device
    Distribution
    0 states
  • HighUSDA FSIS·008-2024·2024-02-28

    M&P Production Recalls Raw Lamb and Beef Samsa for Undeclared Sesame

    M&P Production LTD is recalling raw lamb and beef samsa products because they contain sesame seeds, a known allergen, that are not declared on the label.

    Product
    M&P Production LTD — M&P Production LTD Recalls Raw Lamb and Beef Samsa Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    4 states
  • HighFDA (Drugs)·D-0342-2024·2024-02-28

    Adrenalin Epinephrine Injection Recalled Due to Incorrect Expiration Date Label

    Henry Schein Inc. and Glove Club HSI Gloves Inc. are recalling 1,099 vials of Adrenalin (Epinephrine) Injection because the expiration date on the repack pouch label is incorrect. The product was distributed nationwide.

    Product
    ADRENALIN — ADRENALIN (EPINEPHRINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1168-2024·2024-02-28

    W&H Surgical Handpiece S-12 Recalled for Incorrect Laser Marking

    W&H Surgical handpiece S-12 devices were incorrectly laser marked with '1:1' instead of the correct '1:2' during production. 160 units are affected.

    Product
    W&H Surgical handpiece S-12. For Surgical treatment of dental hard tissue Model Number: 30061000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-02272024-01·2024-02-27

    Nurture Life Chicken Parm Meal Alert for Undeclared Egg Allergen

    USDA FSIS issued a public health alert for Nurture Life Chicken Parm with Super Veggie Spaghetti due to an undeclared egg allergen. Consumers with egg allergies should not consume the product.

    Product
    FSIS Issues Public Health Alert for Nurture Life Ready-To-Eat Chicken Meal Product Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0869-2024·2024-02-21

    Al Amir Baba Ghannooj Recalled for Undeclared Sesame Allergen

    Al Amir Fresh Foods Baba Ghannooj Grilled Eggplant is recalled for undeclared sesame. The product contains tahini but the label does not list sesame as an ingredient, posing a risk to consumers with sesame allergies.

    Product
    Al Amir Fresh Foods Baba Ghannooj Grilled Eggplant, packaged in round plastic clear container, net wt. 8oz. There are 12 containers per case. UPC on 8oz container: 7 55134 12342 1. The recalled product label declares: Ingredients: Fresh Grilled Eggplant, Tahini Paste, Garlico (F
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0872-2024·2024-02-21

    Woodstock 5 Grain Cereal recalled for undisclosed wheat allergen

    Woodstock 5 Grain Cereal is recalled because triticale, a product ingredient, is not identified as wheat on the label. This creates a risk for people with wheat allergies.

    Product
    Woodstock 5 Grain Cereal. Oats, Rye, Triticale, Barley, Golden Flax. Net Wt. 18.5 oz (1 lb 2.5 oz) 524g. UPC 0 42563-01772 9. Distributed by Woodstock, 313 Iron Horse Way, Providence, RI 02908. Packaged in a plant that also processes wheat.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1086-2024·2024-02-21

    Quidel Sofia 2 Flu + SARS Test Kits Recalled for Incorrect Expiration Dates

    Quidel Corporation is recalling one lot of Sofia 2 Flu + SARS Antigen FIA diagnostic test kits due to incorrect expiration dates on packaging. Kits labeled to expire April 30 and May 31, 2025 actually expire September 12, 2024.

    Product
    The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a sandwich design that is used with Sofia 2 to detect nucleocapsid protein from influenza A, influenza B, and SARS-CoV-2. This test allows for the detection of SARS-CoV and SARS-CoV-2, but does not differ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0862-2024·2024-02-14

    Wegmans Petite Pastry Tray recalled for undeclared soy lecithin

    Wegmans is recalling 24ct Petite Pastry Tray croissants due to undeclared soy lecithin. The affected products were distributed across nine states from New York to North Carolina.

    Product
    24ct Petite Pastry Tray, plastic tray with white base and clear lid (not a scale label) (UPC: UPC 7789034215)
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-0860-2024·2024-02-14

    Wegmans Chocolate Croissants Recalled for Undeclared Soy Lecithin

    Wegmans has recalled chocolate croissants containing undeclared soy lecithin due to allergen risk. The recall affects 10,338 units distributed across nine states.

    Product
    5 oz 2pk Chocolate Croissant, bakery box with clear top (UPC 7789050655) and Chocolate Croissant 2 oz, bakery box with clear top (UPC 7789048398)
    Category
    Food
    Distribution
    9 states