The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 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 589 (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.

7526–7550 of 9611

  • ModerateFDA (Food)·F-1592-2014·2014-03-05

    Newman's Own Coffee K-Cups Recalled for Decaffeinated Labeling Errors

    Green Mountain Coffee Roasters is recalling 8,928 boxes of Newman's Own Organic Coffee K-Cups because some caffeinated packs were incorrectly labeled as decaffeinated.

    Product
    Newmans Own¿ Organics Newmans Special Blend 80 Count K-Cup¿ Packs; UPC 09955515593; Product Code: 15593 281792
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-1121-2014·2014-03-05

    Medtronic Everest 20cc Inflation Device Recalled for Incorrect Master Label

    Medtronic Vascular is recalling 191 Everest 20cc Inflation Devices due to an incorrect master label. The devices are sterile, single-use tools used to inflate balloon catheters.

    Product
    Medtronic Everest 20cc Inflation Device; Model Number and Catalog Number: AC2205P The Everest 20cc Inflation device is designed to be used to inflate / deflate balloon catheters as well as to monitor pressure within the balloon. The Everest 20atm Device is outfitted with a man
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V077000·2014-02-27

    Forest River Wildcat Recalled for Incorrect Weight Certification Label

    Forest River is recalling 2014 Wildcat recreational vehicles because the certification tag lists an incorrect gross vehicle weight rating, which could lead to overloading and tire failure.

    Product
    FOREST RIVER — FOREST RIVER WILDCAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1539-2014·2014-02-26

    Mid Pac Foods Recalls Char Sui Sauce for Undeclared Wheat

    Mid Pac Foods is recalling Char Sui sauce because it contains wheat, a major allergen, that is not listed on the label.

    Product
    Mid Pac Foods brand sauce for Char Sui; Net 7 FL. oz (207 ml); Made in Hawaii, Keep in cool place UPC: 7336620250 Manufactured by Mid Pac Foods, Inc. Honolulu, HI.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1535-2014·2014-02-26

    Kinnikinnick Gluten-Free Waffles Recalled for Undeclared Milk Allergen

    DPI Specialty Foods is recalling Kinnikinnick gluten-free waffles because they may contain undeclared milk, despite labeling indicating the product is dairy-free.

    Product
    Kinnikinnick Gluten Free Original Homestyle Waffles Frozen Contains a logos on the package indicating it is gluten free, dairy free, and nut free. 210 g/7.4oz Qty/pkg - 6. UPC 62013300198 1. DPI item # 55844.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0986-2014·2014-02-26

    Synthes 3.2 mm Guide Wire Recalled for Incorrect Raw Material Labeling

    Synthes, Inc. is recalling 3.2 mm Guide Wires because the label lists an incorrect raw material. The recall covers units distributed in the USA, Canada, and Switzerland.

    Product
    Synthes 3.2 mm Guide Wire 400mm. Used for guiding the TFN Helical Blade and TFN Lag Screw into the femoral.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1058-2014·2014-02-26

    BioHorizons Recalls Dental Implants with Incorrect Length Labeling

    BioHorizons is recalling 119 units of dental implants labeled as 10.5mm but actually measuring 12mm. The recall addresses a labeling error regarding the product's physical dimensions.

    Product
    External Implant RBT, D3 Threadform 4.0 X 10.5mm, REF 40105D3, STERILE R, Rx Only, BioHorizons(R), 2300 Riverchase Center, Birmingham, AL 35244 Usage: dental
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0992-2014·2014-02-26

    Synthes Matrix Mandible Short Threaded Drill Guide Recall for Labeling Error

    Synthes, Inc. is recalling 12 units of Matrix Mandible Short Threaded Drill Guides because they have a gray band instead of the green band shown in the guide.

    Product
    Synthes Matrix Mandible Short Threaded Drill Guide intended for oral, maxillofacial surgery; trauma and reconstructive surgery, specifically for fractures of the subcondylar region of the mandible and fractures of the condylar basis region of the mandible.
    Category
    Medical Device
    Distribution
    3 states
  • CriticalFDA (Food)·F-1486-2014·2014-02-19

    Kinnikinnick Gluten-Free Bread Crumbs Recalled for Undeclared Milk

    Unified Western Grocers is recalling Kinnikinnick Gluten Free Bread Crumbs Panko Style due to undeclared milk, despite labels indicating the product is dairy-free.

    Product
    Kinnikinnick Gluten Free Bread Crumbs Panko Style - gluten free, dairy free, nut free. 350g/12.5oz. UPC 62013360015 3 2
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1479-2014·2014-02-19

    Braum's Panko Bread Crumbs Recalled for Undeclared Milk

    Braum's Ice Cream and Dairy is recalling Panko Style Bread Crumbs because they contain undeclared milk. The product was distributed in five states.

    Product
    Panko Style Bread Crumbs net wt. 350g 12.5 oz. gluten free, dairy free, nut free
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1488-2014·2014-02-19

    Kinnikinnick Frozen Waffles Recalled for Undeclared Milk

    Unified Western Grocers is recalling Kinnikinnick Gluten Free Original Homestyle Waffles because they contain undeclared milk despite being labeled as dairy-free.

    Product
    Kinnikinnick Gluten Free Original Homestyle Waffles Frozen Contains a logos on the package indicating it is gluten free, dairy free, and nut free. 210 g/7.4oz Qty/pkg - 6. UPC 62013300198 1.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1494-2014·2014-02-19

    Natures Best Recalls Waffles and Pancakes for Undeclared Milk

    Natures Best is recalling Kinnikinnick pancake and waffle products due to undeclared milk. The recall is nationwide.

    Product
    Original Homestyle Waffles, 7.4oz, Qty/Pkg: 6, UPC 620133001981, NB Item #616953
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1495-2014·2014-02-19

    Natures Best Recalls Waffles and Pancakes for Undeclared Milk

    Natures Best is recalling Kinnikinnick pancake and waffle products because they contain undeclared milk.

    Product
    Cinnamon and Brown Sugar Homestyle Waffles, 7.4oz, Qty/Pkg: 6, UPC 620133001998, NB Item #616961.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1475-2014·2014-02-19

    Farm To Market Bread Co. Sourdough Recalled for Undeclared Wheat

    Farm To Market Bread Co. is recalling San Francisco Sourdough bread because the label fails to list wheat flour, an undeclared allergen.

    Product
    Farm To Market Bread Co. San Francisco Sourdough, net weight 1 lb., unbleached enriched flour, water, sea salt, vitamin C. Farm to Market Bread Co., Kansas City, MO.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1493-2014·2014-02-19

    Natures Best Pancake and Waffle Mix Recalled for Undeclared Milk

    Natures Best is recalling specific lots of Kinnikinnick pancake and waffle mix due to undeclared milk.

    Product
    Pancake and Waffle Mix, 16 oz, UPC 620133105122, NB Item#645556
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1487-2014·2014-02-19

    Kinnikinnick Gluten-Free Pancake and Waffle Mix Recalled for Undeclared Milk

    Unified Western Grocers is recalling Kinnikinnick Gluten Free Pancake and Waffle Mix due to undeclared milk, despite the label indicating the product is dairy free.

    Product
    Kinnikinnick Gluten Free Pancake and Waffle Mix, gluten free, dairy free, nut free. 454 g/ 16 oz UPC 62013300512 2
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1489-2014·2014-02-19

    Kinnikinnick Frozen Waffles Recalled for Undeclared Milk Allergen

    Unified Western Grocers is recalling Kinnikinnick frozen waffles due to undeclared milk, despite labels indicating the product is dairy-free.

    Product
    Kinnikinnick Gluten Free Cinnamon and Brown Sugar Homestyle Waffles - Frozen - gluten free, dairy free, nut free. 210 g/7.4oz Qty/pkg - 6 UPC 62013300199 8
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-1085-2014·2014-02-19

    Actavis Recalls Trelstar Injectable Suspension Due to Labeling Error

    Actavis is recalling 99 cartons of Trelstar 11.25 mg due to a labeling error where the vial was marked 3.75 mg. The product was distributed nationwide and in Puerto Rico.

    Product
    Trelstar (triptorelin pamoate) for Injectable Suspension Single-Dose Vial (NDC 52544-154-02) plus MIXJECT Single-Dose Delivery System containing 2 mL Sterile Water for Injection, USP per carton (NDC 52544-188-76), 11.25 mg, Rx Only, Dist. By: Watson Pharma, Inc., Morristown, NJ 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0939-2014·2014-02-19

    RTI Surgical Recalls OPTEFORM Allograft Paste Due to Incorrect Dispenser

    RTI Surgical, Inc. is recalling 14 units of OPTEFORM Allograft Paste 5cc because they may contain a 10cc fluid dispenser with incorrect fill lines.

    Product
    ***REF 606-01-05***OPTEFORM Allograft Paste 5 cc, bone void filler of bony defects in dental and orthopedic applications.***STERILE Using Radiation. ***Rx Only***Distributor: EXACTECH 2320 NW 66th Court, Gainesville, FL 32653 USA***Manufacturer: RTI Biologicals, Inc. 11621 Resea
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0977-2014·2014-02-19

    Medtronic GRAFTON DBM Flex Recalled for Incorrect Product Dimensions

    Medtronic is recalling GRAFTON DBM Flex units labeled as 2.5 cm x 10 cm that actually measure 2.5 cm x 5 cm.

    Product
    Medtronic GRAFTON (R) DBM, Flex 2.5cm x 10cm, REF T42100, Rx only, STERILE A, QTY: 1 EA, Medtronic Sofamor Danek, USA, Inc., 1800 Pyramid Place, Memphis, TN 38132 Orthopaedic - filler, bone void
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Food)·F-1465-2014·2014-02-12

    Lenguita Cookies Recalled for Undeclared Wheat Allergen

    Gotera, Inc is recalling Lenguita Cookies because the product contains undeclared wheat. The recall affects 217 cases distributed across nine states.

    Product
    Lenguita Cookies net wt. 6 oz., Distributed by Mama Lycha Foods, Houston TX 77055 toll free (877)MAMALYCHA email [email protected] www.mamalycha.com Product of Honduras
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0922-2014·2014-02-12

    Highland Metals Recalls SuperElastic NiTi Archwires Due to Labeling Errors

    Highland Metals, Inc. is recalling SuperElastic NiTi archwires because some packages labeled 'Upper' contain 'Lower' archwires and vice versa.

    Product
    SuperElastic Regular force NiTi lower or upper Natural arches. 0.16 size 10 or 100 count packages. Highland Metals Inc. San Jose, CA The devices are intended to provide force to the teeth to effect movement in order to alter their position.
    Category
    Medical Device
    Distribution
    7 states