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.

1276–1300 of 9606

  • LowFDA (Drugs)·D-0256-2022·2021-12-01

    Butalbital/APAP/Caf Tablets Missing Controlled Substance Label

    Bryant Ranch Prepack is recalling Butalbital, APAP, and Caffeine 50/325/40 mg tablets because the label is missing the controlled substance classification "CIII" required by law.

    Product
    Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b) 60-count bottles, NDC: 63629-8392-03, barcode 083923152614; c) 90-count bottles, NDC:63629-8392-04, barcode 083924152614, Lannett Company Inc; Rx only, Packaged
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0257-2022·2021-12-01

    Butalbital, APAP, Caffeine Tablets Missing Schedule III Label

    Bryant Ranch Prepack is recalling Butalbital, APAP, Caffeine 50/325/40 mg tablets in multiple bottle sizes because the controlled substance classification "CIII" is missing from the label.

    Product
    Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC: 71335-1767-09, barcode 083929164865; b) 20-count bottles, NDC: 71335-1767-01, barcode 083921157837; c) 30-count bottles, NDC: 71335-1767-02, barcode 083922165687, d) 60-count bottles, NDC: 71335-1767-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0228-2022·2021-11-24

    Beaver Xstar Crescent Knife Surgical Blades Recalled for Wrong Blade Orientation

    Beaver Visitec International recalls CustomEyes Cataract Surgical Kits containing Xstar Crescent Knives with incorrect blade orientation. Kits labeled as 55-degree bevel-down blades actually contain bevel-up blades.

    Product
    bvi CustomEyes Kit-AMO Germany GmbH Katarakt-set - Dr. Wagner: CustomEyes Cataract Surgical Kits that contain Beaver Xstar¿ Crescent Knife (REF#373809) as a component a) REF# 588221 REF#: 373809
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0265-2022·2021-11-24

    Smith & Nephew EVOS Self-Tapping Locking Screws recalled due to switched package labels

    Smith & Nephew is recalling 224 units of EVOS Self-Tapping Locking Screws because package labels were switched, creating a risk that incorrect screw sizes could be implanted during surgery.

    Product
    Smith and Nephew EVOS Self-Tapping Locking Screw SST: (1)REF 72413575, 3.5MM x 75MM, and (2) REF 72413570, 3.5MM X 70MM. Sterile.
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0230-2022·2021-11-24

    Surgical Crescent Knife Recalled for Incorrect Blade Orientation Labeling

    Beaver Visitec International is recalling bvi CustomEyes Kits containing Crescent Knives due to incorrect labeling. Products labeled as 55-degree bevel-down blades actually contain bevel-up blades.

    Product
    bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component-non-sterile sample for evaluation purposes REF# BVI 58000587
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0227-2022·2021-11-24

    Beaver Xstar Crescent Knife surgical blades may have incorrect bevel angle

    Approximately 5950 Beaver Xstar Crescent Knife surgical blades may be packaged with the wrong bevel angle, potentially affecting proper surgical technique during cataract procedures.

    Product
    Beaver Xstar Crescent Knife, 2.5mm, 55 degrees, bevel down. Intended for or cataract surgery. REF#: 373809
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0221-2022·2021-11-24

    Simply Fresh Salads Cranberry Walnut Salad Recall for Undeclared Wheat

    Five Star Gourmet Foods is recalling Simply Fresh Salads Cranberry Walnut Salad because wheat allergen is not declared on the label, though flatbread chips containing wheat are visible in the package. The product is distributed in WA, AZ, PA, and TX.

    Product
    Simply Fresh Salads - Cranberry Walnut Salad with Very Berry Vinaigrette; sweet-tart cranberries & Walnuts, feta cheese, crunchy flatbread and spring mix. Keep refrigerated. Net Wt. 4.2 oz. (119g) UPC: 8 50012 79394 6 Contains: Milk, treenut (walnut) Distributed by: FiveStar
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-0232-2022·2021-11-24

    Cartia XT Diltiazem Hydrochloride Capsules Recalled for Incorrect Expiration Date

    Teva Pharmaceuticals USA is recalling Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules, USP) 120 mg due to an incorrect expiration date printed on the label. The affected lot was distributed nationwide.

    Product
    CARTIA — CARTIA (DILTIAZEM HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·21V915000·2021-11-22

    Thomas Built Buses Saf-T-Liner HDX Recalled for Incorrect Weight Label

    Daimler Trucks North America is recalling one 2021 Thomas Built Buses Saf-T-Liner HDX transit bus because the gross axle weight rating label may be incorrect.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0121-2022·2021-11-17

    Sundelight Golden Raisins Recalled for Undeclared Sulfites

    Best Foods NJ, Inc. is recalling Sundelight Golden Raisins due to undeclared sulfites. The product was distributed to retail stores in Maryland, New Jersey, and New York.

    Product
    Sundelight Golden Raisins Net Wt 7oz. UPC: 14760 84059. Plastic pouches. 20 pouches/per case
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-0157-2022·2021-11-17

    NOW Bee Pollen 500mg Capsules Recalled for Metronidazole Contamination

    NOW Health Group Inc. is recalling NOW Bee Pollen 500mg 100 VCAPS (UPC 733739025203) because the product may contain Metronidazole, an antibiotic not listed on the label.

    Product
    NOW Bee Pollen 500mg 100 VCAPS UPC 733739025203
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Food)·F-0156-2022·2021-11-17

    NOW Ginseng & Royal Jelly supplement may contain Metronidazole

    NOW Health Group Inc. is recalling NOW Ginseng & Royal Jelly 90 VCAPS and MMA Nutrition Ginselin 90 Veg Capsules because the products may contain Metronidazole, an undeclared pharmaceutical ingredient.

    Product
    NOW Ginseng & Royal Jelly 90 VCAPS UPC 733739040077 MMA Nutrition Ginselin 90 Veg Capsules UPC 733739440075
    Category
    Drug
    Distribution
    47 states
  • ModerateFDA (Drugs)·D-0227-2022·2021-11-17

    Ezetimibe and Simvastatin Tablets Recalled for Defective Excipient and Foreign Tablets

    Golden State Medical Supply Inc. is recalling specific lots of Ezetimibe and Simvastatin 10 mg/40 mg tablets because an excipient used in manufacturing failed to meet conductivity specifications, and some bottles were found to contain foreign tablets.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    2 states
  • LowFDA (Drugs)·D-0096-2022·2021-11-17

    Cetirizine Hydrochloride 10 mg Tablets Labeling Error Recall

    A-S Medication Solutions LLC is recalling Cetirizine hydrochloride 10 mg tablets due to a labeling error: bottles were labeled as 90-count when they actually contain 30 tablets.

    Product
    CETIRIZINE — CETIRIZINE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    4 states
  • HighNHTSA·21V877000·2021-11-12

    2021-2022 Forest River Cherokee Travel Trailers Recalled for Incorrect Tire Placard

    Forest River is recalling 2021-2022 Cherokee travel trailers because the tire size and weight rating printed on the Federal Placard are incorrect. This could cause the vehicle to be overloaded and lose control.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0106-2022·2021-11-10

    Picket Fence Creamery White Chocolate Raspberry Ice Cream Recall for Undeclared Soy

    Picket Fence Creamery is recalling White Chocolate Raspberry ice cream because it contains undeclared soy lecithin, which poses a risk to consumers with soy allergies.

    Product
    Picket Fence Creamery, Woodward, IA, White Chocolate Raspberry ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0104-2022·2021-11-10

    Picket Fence Creamery Maple Ice Cream Recall for Undeclared Soy

    Picket Fence Creamery is recalling maple ice cream sold in Iowa grocery stores because it contains undeclared soy lecithin, which poses a hazard to consumers with soy allergies.

    Product
    Picket Fence Creamery, Woodward, IA, Maple ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0095-2022·2021-11-10

    Pharmanex Kids Jungamals dietary supplement missing fish allergen label

    NSE Products, Inc. is recalling Pharmanex Kids Jungamals dietary supplement because the label does not disclose fish allergen present in the product's Vitamin E ingredient.

    Product
    Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets, white bottle, NSE Products Inc., Provo, UT 84601 1-888-PHARMANEX
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0102-2022·2021-11-10

    Picket Fence Creamery Key Lime Pie Ice Cream Recall

    Picket Fence Creamery is recalling Key Lime Pie ice cream due to undeclared wheat and soy lecithin, and lack of gluten-free labeling. The product was distributed to grocery stores in Iowa.

    Product
    Picket Fence Creamery, Woodward, IA, Key Lime Pie! ice cream, in quarts, pints and 1/2 pints
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0199-2022·2021-11-10

    MEDRAD Twist & Go Syringe Recalled Due to Labeling Error

    Bayer Medical Care is recalling 6,950 units of MEDRAD Twist & Go Disposable Syringes due to labeling errors that could cause confusion about syringe compatibility with the MEDRAD Mark 7 Arterion Injection System.

    Product
    The MEDRAD Twist & Go Disposable Syringe 150 mL with Quick Fill Tube is a syringe made from a clear polycarbonate material and is an accessory to the MEDRAD Mark 7 Arterion Injection System. It is designed to be loaded into the injector head of the injection system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0100-2022·2021-11-10

    Picket Fence Creamery Mocha Ice Cream Recalled for Undeclared Soy

    Picket Fence Creamery is recalling Mocha! ice cream in multiple sizes due to undeclared soy lecithin. Consumers with soy allergies who purchased this product should not consume it.

    Product
    Picket Fence Creamery, Woodward, IA, Mocha! ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0105-2022·2021-11-10

    Picket Fence Creamery S'mores Ice Cream Recalled for Undeclared Soy

    Picket Fence Creamery is recalling S'mores ice cream in multiple sizes due to undeclared soy lecithin, which poses a risk to consumers with soy allergies.

    Product
    Picket Fence Creamery, Woodward, IA, S'mores! ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0076-2022·2021-11-10

    Meijer Honey Ham & Cheddar Pretzel Roll Sliders Recall

    Meijer is recalling Fresh From Meijer Honey Ham & Cheddar Pretzel Roll Sliders because they contain undeclared soy lecithin, which poses a risk to consumers with soy allergies.

    Product
    Fresh From Meijer, Honey Ham & Cheddar Pretzel Roll Sliders, 6.24 Oz., Plastic clam-shell - clear lid, black bottom, UPC 7-13733-76501-5
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0099-2022·2021-11-10

    Picket Fence Creamery Ice Cream Recall: Undeclared Soy Lecithin

    Picket Fence Creamery is recalling CowaBrownie! ice cream in multiple sizes due to undeclared soy lecithin. Consumers with soy allergies should not consume this product.

    Product
    Picket Fence Creamery, Woodward, IA, CowaBrownie! ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state