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.

3251–3275 of 9607

  • HighFDA (Food)·F-0009-2019·2018-10-10

    Baker's Service Recalls Meat Flavored Pastry for Undeclared Wheat

    Baker's Service of South Florida, Inc. is recalling 179 cases of Meat Flavored Pastry because the finished product labeling failed to declare wheat.

    Product
    Meat Flavored Pastry. The product is packed in a cardboard box. The firm marks the Meat Flavored Pastry option printed on the box. Labeling on the cardboard box reads in part: WHOLESALE FROZEN BAKERY PRODUCTS, TRACY BAKERY, MEAT FLAVORED PASTRY, HANDLING INSTRUCTIONS, PREPARAT
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0010-2019·2018-10-10

    Baker's Service of South Florida Recalls Cheese Pastry for Undeclared Wheat

    Baker's Service of South Florida, Inc. is recalling 706 cases of Cheese Pastry because the product labeling failed to declare wheat as an ingredient.

    Product
    Cheese Pastry. The product is packed in a cardboard box. The firm marks the Cheese Pastry option printed on the box. Labeling on the cardboard box reads in part: WHOLESALE FROZEN BAKERY PRODUCTS, TRACY BAKERY, CHEESE PASTRY, HANDLING INSTRUCTIONS, PREPARATION & BAKING, INGREDI
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0017-2019·2018-10-10

    Burger-Shaped Chocolate Cookies Recalled for Partially Covered Allergen Information

    Wismettac Asian Foods is recalling Everyburger chocolate cookies because a sticker partially covers the ingredient list and allergen information.

    Product
    EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and 80 items per case UPC 8 055880 00701 0 Manufactured by Bourbon 1-3-1 Ekimae Kashiwazaki Nigata 945-8611 Japan Product of Japan
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Drugs)·D-0009-2019·2018-10-10

    Endo Pharmaceuticals Recalls Robaxin-750 Due to Incorrect Dosage Labeling

    Endo Pharmaceuticals is recalling 2,856 bottles of Robaxin-750 (methocarbamol) because the labels contain incorrect dosage instructions.

    Product
    robaxin-750 (methocarbamol tablets, USP), 750 mg, 100-count bottle, Rx Only, Distributed by: Endo Pharmaceuticals Inc., Malvern, PA 19355; Manufactured by: Kremers Urban Pharmaceuticals Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274; NDC 52244-449-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1992-2018·2018-10-10

    Trader Darwin's Chewable Melatonin Recalled for Misbranding and Wrong Product Contents

    Church & Dwight is recalling Trader Darwin's Chewable Peppermint Flavored Melatonin because bottles contain GABA Calm Sublingual Orange tablets instead.

    Product
    Trader Darwin s Chewable Peppermint Flavored Melatonin Dietary Supplement Number of units per package: 100 tablets Package type: Bottle Units per case: 36
    Category
    Drug
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0060-2019·2018-10-10

    Ortho VITROS Prolactin Reagent Pack Recalled for Biotin Interference

    Ortho Clinical Diagnostics is recalling VITROS Prolactin Reagent Packs because biotin supplements may cause biased test results at lower concentrations than stated in the instructions.

    Product
    VITROS Immunodiagnostic Products - Prolactin Reagent Pack (10758750000111) 1849793
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0018-2019·2018-10-10

    Otsuka Recalls Mislabeled Abilify and Abilify Maintena Physician Sample Kits

    Otsuka is recalling 4,738 physician sample kits of Abilify and Abilify Maintena due to labeling errors, including misspelled product names and missing storage instructions.

    Product
    treatNOW ABILIFY (aripiprazole) / ABILIFY MAINTENA 400-mg (aripiprazole) for extended release injectable suspension. Kit contents 2 packs Abilify Tablets 10 mg (14 day supply) plus 1 Abilfy Maintena Vial Kit.Rx only. Distributed and Marketed by: Otsuka America Pharmaceutical, Inc
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0074-2019·2018-10-10

    Smiths Medical Portex Nasal Oxygen Cannula Recall for Labeling Error

    Smiths Medical ASD Inc. is recalling 13,750 Portex First Breath Nasal Oxygen Cannulas because the 'Manufactured' and 'Use By' labels are transposed, incorrectly suggesting the product expired before it was manufactured.

    Product
    smiths medical portex First Breath Nasal Oxygen Cannula, REF 001292, with Gas Monitoring Line, 305 cm (10ft.) & Male Luer Connector, 213 cm (7ft.) Tubing, & Oxygen Adapter. Product Usage: For the administration of nasal oxygen and humidity to patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0075-2019·2018-10-10

    Smiths Medical Portex Nasal Oxygen Cannula Recalled for Labeling Error

    Smiths Medical ASD Inc. is recalling 850 Portex First Breath Nasal Oxygen Cannulas because the 'Manufactured' and 'Use By' dates are transposed, incorrectly suggesting the product expired before it was made.

    Product
    smiths medical portex First Breath Nasal Oxygen Cannula, REF 001293, with Gas Monitoring Line, 305 cm (10ft.) & Female Luer Connector, 213 cm (7ft.) Tubing, & Oxygen Adapter. Product Usage: For the administration of nasal oxygen and humidity to patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0017-2019·2018-10-10

    Otsuka Recalls Mislabeled treatNOW Abilify Physician Sample Kits

    Otsuka is recalling 17,325 treatNOW Abilify physician sample kits due to labeling errors, including misspelled product names and missing storage instructions.

    Product
    treatNOW ABILIFY (aripiprazole) and ABILIFY MAINTENA (aripiprazole) 400MG for extended release injectable suspension. Kit Contents: 2 packs ABILIFY Tablets 10mg (14 day supply) plus 1 ABILIFY MAINTENA Pre-filled Dual Chamber Syringe Kit. Rx only. Not for sale or reimbursement. Di
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0073-2019·2018-10-10

    Smiths Medical Portex Nasal Cannula Recalled for Labeling Error

    Smiths Medical ASD Inc. is recalling 3,000 Portex First Breath Adult Nasal Cannulas because the 'Manufactured' and 'Use By' labels are transposed, suggesting the product expires before it was manufactured.

    Product
    smiths medical portex First Breath Adult Nasal Cannula, REF 001289, Curved Flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0071-2019·2018-10-10

    Smiths Medical Nasal Cannula Recalled for Transposed Date Labels

    Smiths Medical ASD Inc. is recalling 12,000 First Breath Adult Nasal Cannulas because the 'Manufactured' and 'Use By' labels are transposed, incorrectly suggesting the product expired before it was manufactured.

    Product
    smiths medical portex First Breath Adult Nasal Cannula, REF 001283, Non-flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0072-2019·2018-10-10

    Smiths Medical Nasal Cannula Recalled for Incorrect Labeling

    Smiths Medical ASD Inc. is recalling 2,550 adult nasal cannulas because the 'Manufactured' and 'Use By' labels are transposed, suggesting the product expired before it was manufactured.

    Product
    smiths medical portex First Breath Adult Nasal Cannula, REF 001285, Flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·086-2018·2018-10-05

    Canteen Recalls Breaded Chicken Tenders for Undeclared Milk Allergen

    Canteen is recalling ready-to-eat breaded chicken tenders because they contain undeclared milk (whey), a known allergen.

    Product
    Compass Group/Canteen — Canteen/Covenco Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Drugs)·D-0081-2019·2018-10-03

    Hetero Labs Recalls Montelukast Sodium Tablets Due to Labeling Error

    Hetero Labs Limited is recalling 98,016 bottles of Montelukast Sodium 10 mg tablets because one lot may contain Losartan Potassium 50 mg tablets.

    Product
    MONTELUKAST SODIUM — MONTELUKAST SODIUM (MONTELUKAST SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1972-2018·2018-10-03

    Men's Health Supplement Recalled for Undeclared Ingredients

    Confidence Inc. is recalling For-Men-10 dietary supplements because they contain undeclared ingredients, including HPMC and artificial colors.

    Product
    FP0392, For-Men-10, All Natural Formula to Overall Men's Health, A Dietary Supplement, 60 Tablets, UPC: 8 92483 00139 7
    Category
    Food
    Distribution
    20 states
  • HighFDA (Food)·F-1986-2018·2018-10-03

    Gotham Greens Classic Pesto Recalled for Incorrect Ingredient Labeling

    Brett Anthony Foods is recalling Gotham Greens Classic Pesto because the ingredient list incorrectly omits milk (parmigiano).

    Product
    Gotham Greens Classic Pesto 6.5 oz. plastic cup, 12 cups per case. Refrigerated. UPC 85392700334
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-1971-2018·2018-10-03

    Confidence Bone-Lock Dietary Supplement Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Bone-Lock dietary supplements containing undeclared ingredients, including Hydroxypropyl Methylcellulose, Titanium Dioxide, and Polyethylene Glycol.

    Product
    FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 00145 8
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Food)·F-1989-2018·2018-10-03

    Trader Joe's Cinnamon Coffee Cake Recalled for Undeclared Soy

    Pin Hsiao & Associates, LLC dba Zen Bakery is recalling Trader Joe's Cinnamon Coffee Cake because it contains undeclared soy lecithin.

    Product
    TRADER JOE'S Cinnamon Coffee Cake; NET WT. 16 OZ (1 LB) 454g; SKU# 94235; UPC: 00942355
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3246-2018·2018-10-03

    Zimmer Biomet Recalls Mislabelled Tibial Nail Due to Size Discrepancy

    Zimmer Biomet is recalling a specific lot of 8.3mm tibial nails that are actually 12mm. The product was distributed only in the Netherlands.

    Product
    Zimmer Natural Nail Tibial Nail - Yellow 8.3mm, Model Number 47249534008 Product Usage - The Zimmer Natural Nail System is intended for temporary fracture fixation and stabilization of the bone. Indications for the Tibial nails include the following in the tibia: Compound an
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-3253-2018·2018-10-03

    Medtronic Diagnostic Catheter Recalled for Incorrect French Size Labeling

    Medtronic is recalling 250 units of DxTerity TRA 5F Diagnostic Catheters because the inner pouch may incorrectly display a 6 French size indicator instead of the correct 5 French size.

    Product
    Medtronic DxTerity(TM) TRA 5F, Diagnostic Catheter, REF U5TRAN35
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Food)·F-1988-2018·2018-10-03

    Caffeine-Free Barq's Root Beer Recalled for Mislabeling

    Swire Coca Cola USA is recalling Caffeine-Free Barq's Root Beer 12 Packs due to mislabeling. The recall covers 2,945 cases distributed nationwide.

    Product
    Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3252-2018·2018-10-03

    Biomet Sports Medicine Drill Bit Recalled for Incorrect Expiration Date Labeling

    Zimmer Biomet is recalling 217 units of Biomet Sports Medicine Juggerknot Long Flex Drill Bits because the expiration date is incorrectly listed on the label.

    Product
    Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone fixation with indications for use in: Shoulder, Foot and Ankle, Knee, Hand and Wrist and Hip repair.Stainless Steel, Sterile Item Number: 110016992
    Category
    Medical Device
    Distribution
    10 states
  • CriticalFDA (Food)·F-1973-2018·2018-09-26

    Market of Choice Recalls Sesame Noodle Salad Vegan for Undeclared Egg

    Market of Choice Inc is recalling Sesame Noodle Salad Vegan in 8 oz. and 16 oz. containers due to undeclared egg. The product was distributed in Oregon.

    Product
    Sesame Noodle Salad Vegan, packaged in 8 oz. or 16 oz. plastic container. UPC of 8 oz. container: 0 211630 203994. UPC of 16 oz. container: 0 211637 807492. The label is read in parts: "***SESAME NOODLE SALAD VEGAN***Soba Noodles (wheat, our, buckwheat, tapioca starch, s
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V677000·2018-09-26

    Daimler FCCC MC Motorhome Chassis Recall for Air Gauge Line Misconnection

    Daimler Trucks North America is recalling 2017-2019 FCCC MC motorhome chassis because primary and secondary air lines were incorrectly connected to the pressure gauges, increasing crash risk.

    Product
    FCCC — FCCC MC
    Category
    Vehicle
    Distribution
    Distributed nationwide