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.

3126–3150 of 9607

  • HighUSDA FSIS·117-2018·2018-11-23

    Chunwei Inc. Recalls Meat and Poultry Products Due to Misbranding and Undeclared Allergens

    Chunwei, Inc. is recalling meat and poultry products because they are misbranded and may contain undeclared allergens and MSG, with no confirmed illness reports.

    Product
    Chunwei, Inc. Recalls Meat and Poultry Products Due to Misbranding and Undeclared Allergens and Monosodium Glutamate
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0621-2019·2018-11-21

    Wegmans Placek Coffee Cake Recalled for Undeclared Milk

    Wegmans Food Markets is recalling Placek Coffee Cake products because they contain undeclared milk, a major food allergen.

    Product
    Wegmans Placek Coffee Cake - 11 oz., UPC 77890 41407 and 22 oz., UPC 77890 39002
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0455-2019·2018-11-21

    Straumann Recalls Neodent GM Mini Conical Abutments Due to Label Mismatch

    Straumann Manufacturing is recalling 21 units of Neodent GM Mini Conical Abutments because the laser-engraved label does not match the item in the package.

    Product
    Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Abutments are intermediary prosthetic components to be installed onto GM implants to support the final prosthesis. They are provided in a rotational shape for the coupling with the prosthesis and in different gingiva
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0467-2019·2018-11-21

    Stryker Recalls Reprocessed Diagnostic EP Catheters Due to Item Number Error

    Stryker Sustainability Solutions is recalling two reprocessed diagnostic EP catheters because they were identified as item # D134903 but are actually item # D134909, which is not approved for reprocessing.

    Product
    Stryker Sustainability Solutions LASSO NAV eco Reprocessed Diagnostic EP Catheters designed to obtain electrophysiological mapping of the cardiac structures of the heart.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0444-2019·2018-11-21

    Espiner Tissue Retrieval System Recalled for Incorrect Volume Labeling

    Espiner Medical Ltd is recalling 230 units of the Eco-Sac Tissue Retrieval System because the label incorrectly states the volume is 1200 ml instead of 1000 ml.

    Product
    Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml EMP160ECO-US-5 (GTIN:5060358120367) Product Usage: Tissue Retrieval sac made from ripstop nylon. The EMP160ECO-US-5 is a semi-automatic sac, which incorporates a monofilament drawstring around the mouth of th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0468-2019·2018-11-21

    Arrow Multi-Lumen CVC Kit Recalled for Labeling Inconsistencies

    Arrow International is recalling 3,640 units of the AGB+ Multi-Lumen CVC Kit because some labels incorrectly state the spring-wire guide size as .032 instead of .025.

    Product
    Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code CDC-45703-B1A - Product Usage: The multiple-lumen catheter permits venous access to the central circulation by the way of the femoral, jugular, or subclavian veins
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0243-2019·2018-11-21

    Right Value Drug Stores Recalls Tadalafil SR 12 mg Capsules for Misbranding

    Right Value Drug Stores, Inc. is recalling Tadalafil SR 12 mg capsules distributed in California due to labeling misbranding.

    Product
    Tadalafil SR 12 mg Capsules packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop 122 Grapevine Hwy. Hurst, TX 76054 817-282-9376 NDC 99999-9969-51
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-0242-2019·2018-11-21

    Right Value Drug Stores Recalls Tadalafil SR 7 mg Capsules for Misbranding

    Right Value Drug Stores, Inc. is recalling Tadalafil SR 7 mg capsules due to misbranding. The affected lots were distributed in California.

    Product
    Tadalafil SR 7 mg Capsules packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop 122 Grapevine Hwy. Hurst, TX 76054. NDC 99999-9970-88
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-0240-2019·2018-11-21

    Right Value Drug Stores Recalls Progesterone SR 100 mg Capsules for Misbranding

    Right Value Drug Stores, Inc. is recalling 6,580 capsules of Progesterone SR 100 mg due to misbranding. The affected product was distributed in California.

    Product
    Progesterone SR 100 mg Capsules, packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop 122 Grapevine Hwy. Hurst, TX 76054 817-282-9376. NDC 99999-0104-55
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-0241-2019·2018-11-21

    Right Value Drug Stores Recalls Progesterone SR 200 mg Capsules for Misbranding

    Right Value Drug Stores, Inc. is recalling specific lots of Progesterone SR 200 mg Capsules due to misbranding. The affected products were distributed in California.

    Product
    Progesterone SR 200 mg Capsules, packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop 122 Grapevine Hwy. Hurst, TX 76054 817-282-9376. NDC 99999-0018-74
    Category
    Drug
    Distribution
    1 state
  • HighUSDA FSIS·115-2018·2018-11-19

    Deleite Foods Recalls Marinated Chicken Thigh Meat Due to Undeclared Allergens

    Deleite Foods Enterprises is recalling approximately 11,000 pounds of marinated raw chicken thigh meat because the labels fail to declare wheat and soy allergens.

    Product
    Deleite Foods Enterprises, Inc. Recalls Poultry Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0431-2019·2018-11-14

    New Seasons Market Hot & Sour Broth Recalled for Undeclared Soy

    New Seasons Market LLC is recalling 1,908 jars of Hot & Sour Broth because the product contains soy but the label does not declare it.

    Product
    New Seasons Market Hot & Sour Broth, packaged in 24 oz glass jar. UPC 840600108672
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0370-2019·2018-11-14

    Village Baker Cinnamon Chip Sourdough Recalled for Undeclared Allergens

    Artisan Baking Company is recalling Village Baker Cinnamon Chip Sourdough because the label fails to declare milk powder and soy lecithin.

    Product
    Village Baker SPECIALTY ARTISAN BREADS CINNAMON CHIP SOURDOUGH. The product is whole sliced loaves packed in clear plastic bags that are closed with a twist tie. The net weight is 1.5 lbs. The loaves were sold as individual units. The UPC is 6 42739 00121 9. The product's la
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0366-2019·2018-11-14

    Tropical Dreams Ice Cream Recalled for Undeclared Soy and Coconut Allergens

    Edney and Sellers, Ltd. is recalling Tropical Dreams Super Premium Ice Cream in Hawaii because soy oil and coconut were not declared on the label.

    Product
    Tropical Dreams Super Premium Ice Cream Chocolate Coconut Macadamia Nut; Pint container; UPC 7 18122 41477 2 Ingredients: Cream, Sugar, Skim milk powder, water, cocoa powder, dark chocolate, pure vanilla, macadamia nuts, corn syrup, barley malt, carob bean gum and guar gum (s
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0371-2019·2018-11-14

    Fred Meyer Recalls Mislabeled Cornbread Sold as Angel Food Cake Bar

    Fred Meyer Inc. is recalling 432 units of cornbread mislabeled as Angel Food Cake Bar due to undeclared milk and soy allergens.

    Product
    Product 8x8 " individually packaged in black plastic trays with clear plastic dome lid is cornbread and it was MIS-LABELED as Angel Food Cake Bar. The label of Angel Food Cake Bar has the UPC 111110-02100. The label is read in parts: "***Angel Food Cake Bar *** Net wt. 12
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0368-2019·2018-11-14

    Tropical Dreams Vegan Chocolate Ice Cream Recalled for Undeclared Soy Oil

    Edney and Sellers, Ltd. is recalling Tropical Dreams Super Premium Ice Cream Vegan Chocolate because soy oil was not declared on the package label.

    Product
    Tropical Dreams Super Premium Ice Cream Vegan Chocolate ; Pint container; UPC 685450676526 Ingredients: Coconut milk, organic sugar, water, cocoa powder, malt syrup. . Food Allergy warning: This product was prepared at facilities where milk, eggs, wheat, peanuts, tree nut
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0367-2019·2018-11-14

    Tropical Dreams Ice Cream Recalled for Undeclared Soy Oil

    Edney and Sellers, Ltd. is recalling Tropical Dreams Super Premium Ice Cream in Toasted Coconut flavor because soy oil was not declared on the label.

    Product
    Tropical Dreams Super Premium Ice Cream Toasted Coconut; Pint container; UPC 7 66150 09985 0 Ingredients: Cream, Sugar, coconut milk powder, water, toasted coconut, carob bean gum and guar gum (stabilizer), dextrose. Food Allergy warning: This product was prepared at facil
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0223-2019·2018-11-14

    Tailor Made Compounding Recalls Tesamorelin Vials Due to Incorrect Expiration Dates

    Tailor Made Compounding is recalling 10,280 vials of Tesamorelin because the labels indicate a 1-year expiration date instead of the correct 6-month date.

    Product
    Tesamorelin, 1mg/vial, 6mL vial, Lyophilized Powder for Reconstitution and Subcutaneous Injection, Rx Only, Tailor Made Compounding, Nicholasville, KY 40356
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0399-2019·2018-11-14

    Zimmer Biomet Recalls StageOne Hip Cement Spacer Molds

    Zimmer Biomet is recalling 72 units of StageOne Hip cement spacer molds due to a potential for comingling of 43MM and 51MM sizes.

    Product
    StageOne Hip, Models 431207 & 431209Usage: Product Usage: The single-use cement spacer molds are sterile disposables made of medical grade silicone with a 316L stainless steel reinforcement stem. They are designed to be filled with polymethylmethacrylate/gentamicin bone cem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0369-2019·2018-11-14

    Tropical Dreams Vegan Coconut Ice Cream Recalled for Undeclared Soy Oil

    Edney and Sellers, Ltd. is recalling Tropical Dreams Super Premium Ice Cream Vegan Coconut because soy oil was not declared on the package label.

    Product
    Tropical Dreams Super Premium Ice Cream Vegan Coconut; Pint container; UPC: 7 66150 09985 0 Ingredients: Coconut milk, organic sugar, carob bean gum and guar gum (stabilizer), dextrose. Food Allergy warning: This product was prepared at facilities where milk, eggs, wheat,
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0218-2019·2018-11-14

    Janssen Recalls Ortho-Novum 7/7/7 Tablets Due to Incorrect Dispenser Instructions

    Janssen Pharmaceuticals is recalling Ortho-Novum 7/7/7 tablets because the packaging included instructions for the wrong type of pill dispenser.

    Product
    Ortho-Novum 7/7/7 (norethindrone/ethinyl/estradiol) Tablets, 0.5 mg/0.035 mg, 0.75 mg/0.035 mg, 1 mg/0.035, 28-Day Regimen per pouch, packaged in a) 6 Veridate Tablet Dispensers and 6 Refill pouches (NDC 504-58-178-28) per carton (NDC 50458-178-06); and b) 12 Veridate Tablet Disp
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0405-2019·2018-11-14

    Integrity Implants Recalls FlareHawk Interbody Fusion System Instructions for Use

    Integrity Implants is correcting Instructions for Use for the FlareHawk Interbody Fusion System due to discrepancies in cleaning parameters.

    Product
    FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product Usage: Indicated for spinal intervertebral body fusion with autogenous bone graft in skeletally mature individuals with degenerative disc disease.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0403-2019·2018-11-14

    DT MedTech Recalls Ankle Implant Due to Incorrect Package Labeling

    DT MedTech is recalling specific talar implants for ankle joints because the package labels incorrectly identify the device.

    Product
    DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE 4 Part Number: 302114 components are prostheses for a mobile bearing ankle joint.
    Category
    Medical Device
    Distribution
    0 states