The Recall Desk

Hazard

Mislabeling recalls

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

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mislabeling 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.

126–150 of 256

  • HighFDA (Food)·F-1520-2023·2023-09-27

    Circle K Honey Roasted Peanuts recalled for undeclared soy and wheat allergens

    Mount Franklin Foods is recalling Circle K Honey Roasted Peanuts nationwide due to mislabeling that may result in undeclared soy and/or wheat allergens. Consumers with allergies to these substances should not consume this product.

    Product
    Circle K Honey Roasted Peanuts, Net Wt 2.5 oz, UPC 194283102596
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1519-2023·2023-09-27

    Trail Mix Products Recalled for Undeclared Soy and Wheat Allergens

    Mount Franklin Foods LLC is recalling Circle K Get Up Trail Mix and 7 Select Go! Smart Rise & Shine products nationwide because they may contain undeclared soy and/or wheat allergens due to mislabeling.

    Product
    1. Circle K Get Up Trail Mix, Net Wt 2 oz, UPC 194283102893 2. Circle K Get Up Trail Mix, Net Wt 6 oz, UPC 194283104262 3. 7 Select Go! Smart Rise & Shine, Net Wt 2.5 oz, UPC 00052548681500
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1517-2023·2023-09-27

    Honey Roasted Sunflower Kernels Recalled for Undeclared Soy and Wheat

    Power Snacks Honey Roasted Sunflower Kernels are being recalled nationwide due to potential undeclared soy and wheat allergens from mislabeling. Approximately 88,084 units are affected.

    Product
    Power Snacks Honey Roasted Sunflower Kernels, Net Wt 1 oz; UPC 076500722025
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1521-2023·2023-09-27

    Honey Roasted Cashews Recalled for Undeclared Soy and Wheat Allergens

    Mount Franklin Foods is recalling three varieties of honey roasted cashews nationwide due to undeclared soy and wheat allergens caused by mislabeling.

    Product
    1. 7 Select Cashews Halves & Pieces Honey Roasted, Net Wt 3 oz, UPC 00052548723804 2. 7 Select Cashews Halves & Pieces Honey Roasted, Net Wt 5 oz, UPC 00052548723811 3. Circle K Honey Roasted Cashews, Net Wt 2 oz, UPC 194283102749
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2535-2023·2023-09-20

    Procedural Kits with Ultrasonic Gel Recalled for Inappropriate Use Labeling

    Advance Medical Designs is recalling 117,875 procedural kits containing ultrasonic transmission gel due to mislabeling of use instructions. The recall affects kits distributed to the United States, Canada, United Kingdom, Panama, and Netherlands.

    Product
    Procedural kits containing ultrasonic transmission gel, Item Numbers: a) 20-PC424, b) 20-PC448, c) 20-PC548, d) 20-PC596, e) 20-PC648
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-1147-2023·2023-09-13

    OTC Topical Cream Cartons May Contain Mislabeled Prescription Toothpaste

    Capsaicin Cream 0.025% cartons labeled as pain relief cream may contain Sodium Fluoride 1.1% prescription dental toothpaste instead. Consumers should verify product contents before use.

    Product
    CAPSAICIN — CAPSAICIN (CAPSAICIN)
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-2519-2023·2023-09-13

    Hip Prosthesis Implants Recalled for Size Mismatch Between Label and Device

    Zimmer, Inc. is recalling M/L Taper Hip Prosthesis implants where the outer package labeling and product etch do not match the actual implant size. This mislabeling could lead to implantation of the wrong-sized prosthesis.

    Product
    M/L Taper Hip Prosthesis Extended Offset, Reduced Neck Length, Size 4 (Item Number 00771100640) and Size 6 (Item Number 00771100440)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2444-2023·2023-08-30

    Femoral nail implant recalled for product labeling and packaging mismatch

    Smith & Nephew is recalling 32 units of a femoral nail implant due to labeling mismatch. The package contained 40cm implants but was labeled as 36cm, which could result in incorrect surgical implantation.

    Product
    TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT, REF 71647340, Femur nail
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-1409-2023·2023-08-23

    Dilettante Mocha Cafe Dark Chocolate Truffles Display Placard Allergen Labeling Error

    Dilettante Chocolates recalls display placards for L'Orange Dark Bulk Truffles due to incomplete allergen labeling. The placard's allergen warning does not clearly state milk, though the actual product packaging is correctly labeled.

    Product
    Dilettante Mocha Cafe brand L'Orange Dark Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stor
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2146-2023·2023-07-26

    Aesculap Surgical Needle Recalled for Incorrect Product Code Marking

    Aesculap Implant Systems is recalling Aesculap Surgical Needles (MD610) because they are etched with an incorrect product code. The needles are marked MD611 when they should be marked MD610.

    Product
    Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable Article Number: MD610
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2134-2023·2023-07-19

    Medline Non-Sterile PVP Solution Mislabeled as Sterile

    Medline Industries is recalling 128 units of non-sterile PVP solution incorrectly labeled as sterile. Using a non-sterile product in sterile contexts could create infection risk.

    Product
    MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: OISC HAND BEAR, Model Number DYNJ902348L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23228·2023-06-22

    Boost The Mood Ceramic Mugs Recalled Due to Fire Hazard

    Ceramic mugs labeled "microwave safe" can spark and catch fire when microwaved due to metallic print. About 26,400 units were sold at Ulta Beauty stores and online from October 2022 through March 2023.

    Product
    Boost The Mood Ceramic Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0865-2023·2023-06-14

    Empower Pharmacy Ascorbic Acid Injection Mislabeled as Preserved

    Empower Pharmacy is recalling Ascorbic Acid 500 mg/mL injection solution because vials labeled as preserved are actually preservative-free. The 504 affected vials were distributed nationwide.

    Product
    ASCORBIC ACID PRESERVED INJECTION SOLUTION, 500 mg/mL, 30 mL Sterile Multiple-Dose Vial, RX ONLY, Compounded by: Empower Pharmacy, 5980 W Sam Houston Pkwy N Ste 300 Houston, TX 77041, NDC 72627-2405-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1689-2023·2023-06-14

    TREO Abdominal Stent-Graft Label Does Not Match Actual Device Size

    Bolton Medical is recalling the TREO Abdominal Stent-Graft System because the carton label may not match the actual stent-graft size inside. Implanting the wrong size stent-graft could result in surgical complications.

    Product
    The TREO ABDOMINAL STENT-GRAFT SYSTEM (TREO) consists of four types of implants, specifically a Main Bifurcated Stent-Graft, a Leg Extension Stent-Graft, a Proximal Cuff Stent-Graft and a Straight Iliac Extension Stent-Graft. Each stent-graft is preloaded into its own delivery s
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1697-2023·2023-06-14

    Fluoride Varnish Packaging Error: Wrong Flavor Variant in White Mint Package

    Young Dental Manufacturing is recalling Benco Dental iris 5% fluoride varnish packages labeled White Mint because they may contain Bubblegum varnish instead. The recall affects 344 boxes distributed to Florida, Nevada, and Pennsylvania.

    Product
    BencoDental iris 5% NaF varnish, WHITE MINT ITEM # 4323-635; cavity varnish
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1654-2023·2023-06-07

    Knee Replacement Insert Mislabeled; Contents May Not Match Catalog Number

    Howmedica Osteonics Corp. is recalling TRIATHLON X3 knee replacement bearing inserts because products labeled with one catalog number may actually contain a different specification. This mislabeling could result in incorrect implant sizing during surgery.

    Product
    TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for knee replacement Catalog Number: 5532-G-413-E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0891-2023·2023-05-24

    Duke's Bayou Remoulade Sauce Mislabeled as Gluten-Free Despite Wheat Content

    Duke's Southern Sauces Bayou Remoulade sauce is mislabeled as gluten-free but contains wheat in its soy sauce ingredient. Consumers relying on the false gluten-free label could be harmed.

    Product
    Duke's SOUTHERN SAUCES BAYOU REMOULADE NET WT. 10 FL OZ (296 ml) GLUTEN FREE INGREDIENTS:***SOY SAUCE (WHEAT, SOYBEANS, AND SALT)***CONTAINS SOY, WHEAT, EGGS SAUER BRANDS, INC. RICHMOND, VA 23220 UPC x 52500 08582 7
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1604-2023·2023-05-24

    Dental implant system recalled for incorrect package length labeling

    Hiossen Inc. is recalling 287 units of ET III Nano-HA dental implants due to incorrect package labeling stating implant length as 10mm when the actual length is 8.5mm. No illnesses or injuries have been reported.

    Product
    ET III Nano-HA fixture System ET NH Dental Implant Model # ET3R5010B -Intended for Dental Implant Catalog #: AET3R5010B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0871-2023·2023-05-17

    Takuma Herb Salt Peanuts Recalled for Undeclared Fish Allergen

    Daiso California Warehouse is recalling Takuma food herb salt peanuts because the product contains fish (Bonito, Sardines, Tuna) but does not list it on the label. Consumers with fish allergies could unknowingly consume the product.

    Product
    Takuma food herb salt peanut 80g UPC: 4962679652767
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0876-2023·2023-05-17

    FDA Recalls Kimura Burdock Salt for Undeclared Fish Allergen

    Daiso California Warehouse is recalling Kimura burdock salt because it contains fish (sardines, bonito, tuna) not listed on the label. People with fish allergies may have a serious allergic reaction.

    Product
    Kimura burdock salt 40g UPC: 4972304293524
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0780-2023·2023-05-10

    Soy Flour Products Recalled for Potential Gluten Contamination

    Cargill recalls 977,000 pounds of soy flour products labeled gluten-free that may contain gluten above FDA limits. Products were distributed in the US and multiple countries.

    Product
    PROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB BG/36, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0783-2023·2023-05-10

    Cargill Flour Recalled Due to Undeclared Gluten Contamination

    Cargill is recalling PROSANTE TSOYFLR flour products nationwide and internationally due to potential gluten contamination in products labeled as gluten-free. The recalled products may contain gluten levels above 20 ppm.

    Product
    PROSANTE TSOYFLR 3014P FLK 50LB BG, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0799-2023·2023-05-10

    Cargill recalls bulk ingredient for gluten exceeding safe levels

    Cargill recalls 174,600 lbs of bulk ingredient distributed nationwide and internationally. Products labeled gluten-free contain gluten levels exceeding 20 ppm.

    Product
    PROSANTE TVGPTN 7B MNCD 50LB BG, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0801-2023·2023-05-10

    Cargill Grain Product Recalled for Gluten Contamination Despite Gluten-Free Label

    Cargill is recalling PROSANTE TVGPTN products labeled as gluten-free because they may contain gluten levels above 20 ppm. The recall affects 42,400 pounds distributed nationwide and internationally.

    Product
    PROSANTE TVGPTN 10P MNCD 25LB BG/32P, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0788-2023·2023-05-10

    Soy Flour Recalled for Undeclared Gluten in Gluten-Free Products

    Cargill is recalling PROSANTE TSOYFLR flour products labeled gluten-free because they may contain gluten above 20 ppm. Consumers with celiac disease or gluten sensitivity should not consume these products.

    Product
    PROSANTE TSOYFLR 3P MNCD 50LB BG, paper bag
    Category
    Food
    Distribution
    Distributed nationwide