The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (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.

6126–6150 of 9610

  • HighFDA (Food)·F-0008-2016·2015-10-21

    Old Time Candy Recalls French Burnt Peanuts Due to Allergen Mislabeling

    Old Time Candy is recalling 72 containers of French Burnt Peanuts because the packaging fails to list peanuts, sugar, artificial colors, and salt as ingredients.

    Product
    French Burnt Peanuts, NET WEIGHT 8 OZ (227g) Old Time Candy.com Distributed by Old Time Candy Company LaGrange, OH 44050 www.oldtimecandy.com Ingredients: Dextrose, Citric Acid, Calcium Stearate, Artificial Flavors, Artificial Colors***. May Contain Milk And Soy.
    Category
    Food
    Distribution
    29 states
  • ModerateFDA (Drugs)·D-0018-2016·2015-10-21

    Mentholatum Recalls WellPatch Capsaicin Patches Due to Labeling Error

    The Mentholatum Company is recalling WellPatch Capsaicin Pain Relief Patches because the word 'not' was missing from safety instructions, potentially leading to improper use.

    Product
    WellPatch¿ Capsaicin Pain Relief Patch, 0.025% Natural Capsaicin, External Analgesic, 4 Large Patches, Distributed by Consignor; The Mentholatum Company, Orchard Park, NY, Manufactured by Consignee; Mentholatum (China) Pharmaceuticals, Guangdong China --- NDC 10742-8126-2, UPC 31
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0009-2016·2015-10-21

    Win Luck Recalls Glutinous Rice for Undeclared Alcohol Content

    Win Luck Trading Inc is recalling Grove Grow Notes Glutinous Rice because it contains undeclared alcohol. The product was distributed in New Jersey.

    Product
    Glutinous Rice, Net WT. 1000 g, packaged in plastic bottles, UPC 6958020881168, Made in China
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0122-2016·2015-10-21

    Alere Cholestech LDX Multianalyte Controls Recalled for Incorrect Ranges

    Alere San Diego is recalling Cholestech LDX Multianalyte Controls because the assigned control ranges for Total Cholesterol and Triglycerides are incorrect.

    Product
    Alere Cholestech LDX Multianalyte Controls, PN 88769 and 88773. Enables users to monitor the performance of total cholesterol (TC), high density lipoprotein cholesterol (HDL), triglycerides (TRG) and glucose (GLU) test procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0126-2016·2015-10-21

    Synthes Screw Inserter Recalled for Incorrect Etched Graphics

    Synthes (USA) Products LLC is recalling 793 units of the Screw Inserter because the etched graphics may not correspond to the instrument's actual angle.

    Product
    Synthes Screw Inserter; for use with Intramedullary Rod, orthopedic device. Used to secure the head element to the head element inserter to prevent disengagement during head element insertion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0124-2016·2015-10-21

    Synthes Humerus Plates Recalled for Incorrect Part Number Labeling

    Synthes (USA) Products LLC is recalling 36 units of VA-LCP Humerus Plates because one part number was incorrectly etched on the device.

    Product
    Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm- Sterile and Synthes 2.7MM/3.5MM VA-LCP Extended Medial Distal Humerus Plates 10H/RT/189mm-Sterile The Synthes 2.7 mm/3.5 mm Variable Angle LCP Elbow System is intended for fixation of fractures of the distal
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Devices)·Z-0120-2016·2015-10-21

    Ev3 Neurovascular Recalls Pipeline Embolization Devices Due to Incorrect Instructions

    Micro Therapeutics Inc, dba Ev3 Neurovascular, is recalling 23 Pipeline and Pipeline Flex Embolization Devices because they were shipped with EU-version Instructions for Use.

    Product
    -Pipeline Embolization Device -Pipeline Flex Embolization Device The Pipeline and Pipeline Flex Embolization Devices consist of a permanent implant combined with a guidewire based delivery system. The Pipeline and Pipeline Flex embolization device implant is a braided, multi
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0127-2016·2015-10-21

    Arrow International Recalls PICC Catheters Due to Labeling Inaccuracy

    Arrow International Inc is recalling 4FR Single Lumen Pressure Injectable PICC catheters because the instructions state they withstand 10 pressure injections, but they are only tested for 5.

    Product
    4FR Single Lumen Pressure Injectable PICC; intravascular therapeutic catheter, for long-term use greater than 30 days.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·128-2015·2015-10-20

    Taylor Farms Recalls Turkey Meatloaf Due to Undeclared Allergens

    Taylor Farms is recalling approximately 276 pounds of turkey meatloaf products because they contain undeclared eggs, soy, and wheat.

    Product
    Taylor Farms New Jersey, Inc. — Taylor Farms Recalls Turkey Meatloaf Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·15V670000·2015-10-19

    Utilimaster Walk-In Van Recall for Incorrect Tire Placard Cargo Capacity

    Spartan Motors USA is recalling 2014-2015 Utilimaster Walk-In Vans because the tire placard may display incorrect cargo capacity information, potentially leading to vehicle overload.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0005-2016·2015-10-14

    Caribou Coffee Recalls Biscotti for Missing Soy Ingredient Labeling

    Caribou Coffee Company Inc. is recalling two types of biscotti because soy lecithin was missing from the ingredient list.

    Product
    Caribou Chocolate Chip Toffee Pecan Biscotti, Net Wt. 1.4 oz. (40g) in clear cello flow wrap bag.
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-0105-2016·2015-10-14

    CooperSurgical LEEP REDIKIT Recalled for Incorrect Lidocaine Concentration Labeling

    CooperSurgical is recalling LEEP REDIKIT surgical kits because the labels list 2% Lidocaine HCl, but the kits contain 1% Lidocaine HCl vials.

    Product
    CooperSurgical LEEP REDIKIT-Used as a surgical preparatory kit for Loop Electrosurgical Excision Procedure P/N 6061
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-0027-2016·2015-10-14

    Zimmer Universal Locking System Recalled for Incorrect Silk Screening

    Zimmer, Inc. is recalling 18 units of the Universal Locking System due to incorrect catalog numbers printed on the trays.

    Product
    Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unu
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0022-2016·2015-10-14

    Medtronic SureScan Pacemaker ID Cards Mislabel MR Conditional Status

    Medtronic is recalling 777 identification cards for SureScan pacemaker patients that incorrectly indicate the entire system is MR Conditional.

    Product
    Medtronic Medical Device Identification Card for SureScan pacemaker patients. The front of this card identifies the implanted pacing system components currently registered to the patient. The back of the card lists patient's following physician as well as specific messa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0004-2016·2015-10-14

    Blue Plate Light Mayonnaise Recalled for Incorrect Labeling

    Reily Foods Co. is recalling one lot of Blue Plate Light Mayonnaise because the packaging displays the ingredient and nutrition information for regular Blue Plate Mayonnaise.

    Product
    Blue Plate(R) LIGHT MAYONNAISE, 18 Fl OZ (1 PT 2 OZ) 532, mL. UPC 47900-50638
    Category
    Food
    Distribution
    12 states
  • HighNHTSA·15V645000·2015-10-13

    Forest River Recalls 2015-2016 Trailers for Incorrect Tire Placard

    Forest River is recalling specific 2015 Wildwood and 2016 Salem recreational trailers because the tire and wheel placard lists incorrect sizes, which could lead to vehicle instability if the wrong tires are installed.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V650000·2015-10-13

    Forest River Cherokee Recalled for Incorrect Federal Placard Information

    Forest River is recalling 2013-2014 Cherokee trailers because the Federal placard displays incorrect tire and weight information, which could lead to vehicle overload.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3256-2015·2015-10-07

    Hill Country Fare Spring Water Recalled for Possible Undeclared Milk Allergen

    Hill Country Fare Natural Spring Water is being recalled due to a possible undeclared milk allergen. The product was distributed in Texas.

    Product
    Hill Country Fare Natural Spring Water 1 GAL./3.78L container packaged in polyethylene jug
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-3247-2015·2015-10-07

    Russet House Recalls Frozen Sweet Potato Fries Due to Undeclared Gluten

    Russet House is recalling specific lots of America's Choice frozen sweet potato fries because they contain undeclared gluten. The product was distributed in six northeastern states.

    Product
    America's Choice Straight Cut Sweet Potatoes Fries, Frozen 539 g in plastic bag. Distributed by: ONPOINT Inc. Montvale, NJ. Product of Canada UPC: 7 54807 12025 5
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-3255-2015·2015-10-07

    Real Foods Broccoli Salad Kit Recalled for Undeclared Peanuts

    Real Foods, LLC is recalling 13 cases of Broccoli Salad Kit because peanuts were inadvertently added instead of sunflower seeds, and the label does not declare peanuts.

    Product
    Broccoli Salad Kit, product ID; 028-07092, packaged in a bulk case, Net wt. 11 lbs (4.99 kg). UPC: 0 45009 07092 0 The product is labeled in parts "***BROCCOLI SALAD KIT***Ingredients: Ingredients: Broccoli, Broccoli Slaw (broccoli, carrots, red cabbage), Coleslaw Dressing (hi
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2820-2015·2015-10-07

    Zimmer Recalls Guide Wires Due to Incorrect Expiration Date Labeling

    Zimmer, Inc. is recalling 112,568 sterile guide wires because the labels state a 10-year expiration date, while testing supports only 5 years.

    Product
    Zimmer Guide Wires for orthopedic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-3258-2015·2015-10-07

    Coquette's Gluten Free Cupcakes Recalled for Incorrect Allergen Labeling

    Coquette's Bistro and Bakery is recalling 120 packages of gluten-free cupcakes because the label incorrectly states the product contains no egg or dairy, despite containing both.

    Product
    Coquette's Gluten Free Spring Pack Cupcakes (4 pack), Oranges n' Cream & Strawberry Mint Lemonade. coquettesbistro.com. NET Wt. 9.67 OZ. No expiration date on package, sold in ambient air at retail.
    Category
    Food
    Distribution
    2 states