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.

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.

1401–1425 of 9607

  • HighFDA (Food)·F-0779-2021·2021-07-21

    Living Free Lung & Joint Congestion Herbal Dietary Supplement Soy Allergen

    Bea Lydeckers Naturals Inc is recalling Living Free Lung & Joint Congestion Herbal Dietary Supplement because the label declares lecithin but does not identify it as soy lecithin, creating an undeclared soy allergen hazard.

    Product
    Living Free Lung & Joint Congestion Herbal Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Lung & Joint Congestion Herbal Dietary Supplement***Glandular,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0780-2021·2021-07-21

    Living Free Nerve & Muscle Herbal Dietary Supplement Soy Allergen Undeclared

    Bea Lydeckers Naturals Inc is recalling Living Free Nerve & Muscle Herbal Dietary Supplement because the label declares lecithin but does not specify that it contains soy lecithin, potentially endangering consumers with soy allergies.

    Product
    Living Free Nerve & Muscle Herbal Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Nerve & Muscle Herbal Dietary Supplement***Herbal and Glandular Suppleme
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2079-2021·2021-07-21

    Catheter Sheath Introducer Recalled for Size Labeling Discrepancy

    Cordis Corporation is recalling 680 Avanti® Catheter Sheath Introducer units because the actual product dimensions are larger than the labeling indicates.

    Product
    Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2078-2021·2021-07-21

    Unifine Pentips Plus pen needles distributed with incorrect needle sizes

    Owen Mumford USA is recalling Unifine Pentips Plus pen needles because two cases of 4mm needles were mistakenly packaged as 8mm needles, which could result in patients receiving incorrect needle sizes for their insulin pens.

    Product
    Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0781-2021·2021-07-21

    Living Free Nerve & Muscle Plus Supplement Recalled for Undeclared Soy

    Bea Lydeckers Naturals Inc is recalling Living Free Nerve & Muscle Plus Cetyl-Myristoleate supplement because the label declares lecithin but does not declare that the lecithin is soy-derived, posing a risk to consumers with soy allergies.

    Product
    Living Free Nerve & Muscle Plus Cetyl-Myristoleate Herbal and Glandular Supplement, 180 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Nerve & Muscle Plus Cetyl-Myristoleate ***
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0768-2021·2021-07-14

    Jersey Cookie Monster Ice Cream recalled for undeclared soy

    Greenwood Ice Cream is recalling Jersey Cookie Monster Ice Cream because the ingredient statement does not include soy, posing a risk to consumers with soy allergies.

    Product
    JERSEY COOKIE MONSTER ICE CREAM 3 GALLONS (11.34 LITERS) MFG: GREENWOOD ICE CREAM CO LTD 4829 PEACHTREE ROAD, ATLANTA, GA 30341 UPC 0 12609 06378 0
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0756-2021·2021-07-07

    Tulkoff Spicy Kimchi Aioli recalled for undeclared allergens

    Tulkoff Food Products Inc. is recalling Tulkoff Spicy Kimchi Aioli (18 fl oz) due to undeclared soy and wheat allergens. The product was distributed in New Jersey, Pennsylvania, and Maryland.

    Product
    Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09.18.2021M, 8 bottles per case, keep refrigerated
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1996-2021·2021-07-07

    Infusion Pump Order Form Discontinued Due to Ambiguous Reuse Instructions

    Flowonix Medical is recalling physician order forms for Prometra infusion pumps due to ambiguous wording that could be misinterpreted as instructions to reuse previously extracted medication, posing an infection risk.

    Product
    Physician Order Form (PL-15400-00, Nov. 2018) distributed to end user used with the following: Prometra Programmable Infusion Pump System: MODEL/CATALOG #(s): Catalog No. US Model GTIN-14 11827 Prometra Programmable 20mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1993-2021·2021-07-07

    Percutaneous Dilation Tracheostomy Kit Recalled for Incorrect Size Labeling

    One lot of PORTEX ULTRperc Percutaneous Dilation Tracheostomy Kit (Lot 4072715) was incorrectly labeled as 7.0mm when it is 9.0mm. The 40 units were distributed in Pennsylvania, Michigan, Maryland, and Florida.

    Product
    PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit, REF 100/596/090 - Product Usage: intended for use in a controlled setting such as an Intensive Care Unit or operating room with the assistance of trained personnel.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1975-2021·2021-07-07

    PERLA TL Lateral Connector Open Spinal Fusion Devices Recalled for External Label Error

    SPINEART SA is recalling 44 units of PERLA TL Lateral Connector Open spinal fusion connectors distributed in the U.S. due to external labels that incorrectly list the rod size.

    Product
    PERLA TL Lateral Connector Open - Product Usage: intended to be used with autograft and/or allograft. Pediatric pedicle screw fixation is limited to a posterior approach. Models: PERLA TL Lateral Connector Open, 15mm PERLA TL Lateral Connector Open, 30mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0643-2021·2021-07-07

    QiYu Hand Sanitizer Recalled for Subpotent Ethyl Alcohol Content

    HoYu (US) Logistics Inc is recalling QiYu Hand Sanitizer (75% ethyl alcohol) because the product is subpotent. The recall affects 30,880 bottles distributed nationwide.

    Product
    QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui Cosmetics Co., Ltd, Baiyun District, Guanzhou, China Distributed by HoYu (US) Logistics Inc UPC 6 926645 716288
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0755-2021·2021-07-07

    Just Nuts Japanese Style Peanuts recalled for unapproved food dye

    El Presidente Foods is recalling Just Nuts Japanese Style Peanuts (6.17 oz bags, Lot 317-20, expiring July 19, 2021) distributed in California because FDA inspection found the peanuts contained non-approved Red #6 dye.

    Product
    Just Nuts Japanese Style Peanuts, Crunchy coated peanuts. 6.17 oz. polyethene bags. UPC : 1 90236 0000 1 Distributed by El Presidente, Foods Co., Yorba Linda, CA Made in Mexico.
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21V497000·2021-07-01

    2021 GMC Canyon Vehicles Recalled for Incorrect Tire Load Capacity Label

    General Motors is recalling 7,199 2021 GMC Canyon vehicles because the tire and loading information placard lists load capacity 51 pounds higher than intended, increasing the risk of vehicle overload and crashes.

    Product
    GMC — GMC CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0679-2021·2021-06-30

    O'Brien's Own Gourmet Granola Recalled for Undeclared Milk

    O'Brien's Own Gourmet Granola blueberry muffin flavor is recalled because the product contains whey but does not declare milk on the label, creating a risk for consumers with milk allergies.

    Product
    O'Brien's Own Gourmet Granola, blueberry muffin, Net Wt. 12 OZ , UPC 6 09132 49665 3, Manufactured and Distributed by O'Brien's Own Gourmet Granola, Center Point, IA.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0681-2021·2021-06-30

    O'Brien's Own Gourmet Granola Chocolate Peanut Butter Recalled

    O'Brien's Own Gourmet Granola in chocolate peanut butter flavor is being recalled because the product contains whey but does not declare milk on the label, posing a risk to consumers with milk allergies.

    Product
    O'Brien's Own Gourmet Granola, chocolate peanut butter, Net Wt. 12 OZ , UPC 6 09132 49668 4; Manufactured and Distributed by O'Brien's Own Gourmet Granola, Center Point, IA.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0682-2021·2021-06-30

    Su Cocina Pan Molido Bread Crumbs Recalled for Undeclared Milk

    Dominguez Foods of Washington is recalling Su Cocina Pan Molido bread crumbs because the label declares whey but does not declare milk, posing a risk to consumers with milk allergies.

    Product
    Su Cocina Pan Molido bread crumbs in 8 oz. packages. UPC 6 79790 05912 5. The label of 8 oz. package is read in parts: "***Plain Bread Crumbs *** Su Cocina Pan Molido***INGREDIENTS: Enriched wheat Flour ***Corn Starch, Corn Syrup, Water, Contains 2% or less of the following: So
    Category
    Food
    Distribution
    2 states
  • ModerateNHTSA·21V475000·2021-06-25

    Forest River Recalls 2021 East to West Entrada Motorhomes for Placard Error

    Forest River is recalling 2021 East to West Entrada motorhomes because the federal placard incorrectly lists six seat belts instead of four, potentially leaving passengers unsecured.

    Product
    EAST TO WEST — EAST TO WEST ENTRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0628-2021·2021-06-23

    Imperia Elita Vitaccino Coffee Recalled for Unapproved Drug Ingredients

    Imperia Elita Vitaccino Coffee sachets are being recalled because they were marketed without FDA approval and contain pharmaceutical ingredients Sibutramine and Fluoxetine. All lots distributed nationwide are affected.

    Product
    Imperia Elita Vitaccino Coffee, 10 g sachets, 15 sachets per box, Global Beauty Technologies, Manufactured for: Imperia-Elita Ltd. & Co, KG D- 35435 Wettenberg
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1850-2021·2021-06-23

    Hip Prosthesis Stems Mislabeled with Incorrect Size Designation

    Corin Ltd is recalling TriIFit TS size 2 hip prosthesis stems that were labeled incorrectly as TriFit CF size 7 stems, and vice versa. Patients receiving mismatched implants face risk of poor fit and potential complications.

    Product
    Corin TriIFit TS SIZE 2, STANDARD TAPERED STEM, CEMENTLESS, REF 694.0002. Hip prosthesis component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1851-2021·2021-06-23

    Hip prosthesis components recalled for mislabeling with incorrect sizes and types

    Corin TriFit hip prosthesis components from lot 467881 were mislabeled, with size 2 stems labeled as size 7 and vice versa. Surgeons could implant incorrect components during hip replacement surgery.

    Product
    Corin TriFit CF SIZE 7, LATERALISED 127o, COMBINED FIXATION STEM, CEMENTLESS, REF 6961007. Hip prosthesis component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0670-2021·2021-06-23

    Hix Sauces Buffalo Wing Sauce Recall Due to Undeclared Milk Allergen

    Hix Sauces Buffalo Wing Sauce is being recalled because the product label declares butter but does not list milk as an ingredient, creating an allergen risk for consumers with milk allergies.

    Product
    Hix Sauces, Buffalo Wing Sauce, Original Spice, Net Wt. 12.5 oz (355g)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0648-2021·2021-06-23

    Ketamine HCl Injection Solution Recalled for Labeling and Expiration Date Errors

    Prisma Health Outsourcing Facility is recalling Ketamine HCl Injection Solution (10 mg / 2 mL) distributed in South Carolina due to incorrect expiration dates and incorrect Beyond Use Dates (BUD) on the labeling.

    Product
    Ketamine HCl Injection Solution, 10 mg / 2 mL (5 mg/mL), Rx Only, Compounded by Prisma Health Outsourcing Facility 1071 Holland Rd. Suite 2 Simpsonville, SC 29681. NDC: 73463-0100-01
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1834-2021·2021-06-16

    Surgical procedure pack anesthetic mislabeled with wrong drug and strength

    DeRoyal Angio Cath Removal Tray contains mislabeled anesthetic; the label indicates 1% Lidocaine but the tray actually contains 0.5% Bupivacaine. This FDA Class I recall affects 60 trays distributed in MS, VA, LA, and NY.

    Product
    DeRoyal Angio Cath Removal Tray, REF 89-9936.02
    Category
    Medical Device
    Distribution
    Distributed nationwide