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.

451–475 of 9606

  • ModerateFDA (Devices)·Z-2143-2024·2024-06-19

    Darby Dental Prophylaxis Paste Mislabeled with Incorrect Part Number

    Young Dental Manufacturing is recalling 534 units of Darby Prophylaxis Paste with 1.23% Fluoride Ion (Lot 248607) due to incorrect part number labeling. The product was labeled as part number 045032 instead of the correct 040032.

    Product
    Darby Prophylaxis Paste with 1.23% Fluoride Ion, Mint Coarse
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2036-2024·2024-06-19

    NEOMED nonsterile pharmacy syringes recalled for missing expiration dates on labels

    Avanos Medical recalls NEOMED nonsterile pharmacy syringes because expiration dates were not printed on outer shipping labels, resulting in expired products being distributed.

    Product
    NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a. 0.5mL Oral Syringe Blue NonSterile, Product Code BB-S05EO; b. 12mL Oral Syringe Blue NonSterile, Product Code BB-S12EO; c. 1mL Oral Syringe Blue NonSterile, Product Code BB-S1EO; d. 2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1359-2024·2024-06-19

    TriyBrewed Coffee Concentrate Recalled for Missing Ingredient and Nutrition Labels

    Waco Bottling LLC is recalling TriyBrewed Coffee Concentrate 6oz bottles due to missing ingredient statement and nutrition label. Consumers cannot verify product contents or nutritional information.

    Product
    TriyBrewed Coffee Concentrate 6oz/177ml, amber glass bottle, 6pcs to case
    Category
    Food
    Distribution
    0 states
  • HighCPSC·24260·2024-06-13

    Daikin Air Conditioning and Heat Pump Units Recalled for Fire Hazard

    Daikin Comfort Technologies Manufacturing is recalling about 12,100 Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units due to incorrect electrical ratings on the serial plate that could lead to improper wiring and fire risk.

    Product
    Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1299-2024·2024-06-12

    Della Fattoria Sicilian Semolina Bread Recalled for Undeclared Sesame Seeds

    Della Fattoria, LLC is recalling Della Fattoria Sicilian Semolina bread due to missing sesame seed declarations on the label. Consumers with sesame allergies should not consume this product.

    Product
    Della Fattoria Sicilian Semolina
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0538-2024·2024-06-12

    Cephalexin Oral Suspension Recalled for Incorrect Dosage Label

    Bryant Ranch Prepack is recalling Cephalexin oral suspension because the back label incorrectly states the bottle contains 5g instead of 10g. No illnesses have been reported.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0540-2024·2024-06-12

    Cephalexin oral suspension recalled for incorrect dose labeling

    Bryant Ranch Prepack is recalling 61 bottles of Cephalexin for Oral Suspension due to a back label stating an incorrect dose amount—5g instead of 10g per bottle.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0537-2024·2024-06-12

    Cephalexin oral suspension recalled for incorrect label dosage amount

    Bryant Ranch Prepack is recalling Cephalexin oral suspension (125mg/5mL) due to back label errors stating the dose as 2.5g instead of the correct 5g per bottle. No illnesses have been reported.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0539-2024·2024-06-12

    Cephalexin for Oral Suspension Recalled for Back Label Error

    Cephalexin for Oral Suspension is being recalled due to a back label error. The label states 'Each contains' instead of 'Each Bottle contains,' affecting 190 bottles distributed nationwide.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-06102024-01·2024-06-10

    USDA Issues Public Health Alert for Misbranded Southwestern Salad Bowls

    USDA FSIS issued a public health alert for Bistro Grande Southwestern Style salad bowls containing undeclared wheat and fish allergens.

    Product
    FSIS Issues Public Health Alert For Southwestern Style Salad Bowls With Chicken Due To Misbranding And Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighUSDA FSIS·PHA-06072024-01·2024-06-07

    Frozen Bao Curry Chicken Recalled for Undeclared Soy and Sesame Allergens

    USDA FSIS issued a public health alert for frozen bao curry chicken products that may contain undeclared soy and sesame allergens.

    Product
    Brett Anthony Foods — FSIS Issues Public Health Alert for Frozen Ready-To-Eat Bao Curry Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V416000·2024-06-06

    RAM ProMaster vehicles recalled for missing side door beam and incorrect seating label

    Certain 2021-2024 RAM ProMaster vehicles lack a side door beam and have incorrect seating capacity information on the tire placard. These defects may reduce occupant protection in side-impact crashes and could result in improper vehicle loading.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·24T007000·2024-06-03

    Hankook Kinergy GT Tires Recalled for Missing Identification Codes

    Hankook is recalling specific Kinergy GT tires because they lack required week and year codes, making it difficult to identify tires involved in future safety recalls.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24247·2024-05-30

    ADIOS Super Vinegar Cleaner recalled for poisoning and chemical burn risk

    Compare Brands is recalling ADIOS! Super Vinegar All Natural Cleaner due to deceptive labeling that violates federal hazardous-substances rules, posing risks of poisoning and chemical burns.

    Product
    ADIOS! Super Vinegar All Natural Cleaner, 30%
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0508-2024·2024-05-29

    Phenylephrine Injection Recalled Due to Ephedrine Label Mix-Up

    Hikma Injectables USA Inc is recalling phenylephrine injection syringes that were mislabeled as containing ephedrine. The mix-up creates a serious risk of administering the wrong medication to patients.

    Product
    Phenylephrine in 0.9% Sodium Chloride Injection Preservative Free, 100mcg/mL, 5mL syringe, Rx only, Hikma Injectables USA Inc, 36 Stults Road, Dayton, NJ 08810, NDC 63037-123-25
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Food)·F-1252-2024·2024-05-29

    Geissler's Supermarket Pink Lady Salmon Roll Recalled for Undeclared Egg Allergen

    Geissler's Supermarket is recalling Pink Lady Salmon & Avo Roll Combo sushi due to undeclared egg allergen. Consumers with egg allergies risk allergic reactions if they consume this product.

    Product
    Geissler's Supermarket Pink Lady Salmon &Avo Roll Combo (sushi roll) Ingredients read in part: "***INGREDIENTS: SALMON, AVOCADO, WATER. NORI.WHITESTEAMEORICE. VINEGAR. SUGAR. SALT.LEMON.MIRIN. WASABI. GINGER. SOYSAUCE (WHEAT, SOYBEANS,ALCOHOL) HOT SAUCE: SUGAR. MAYO. CHILI, SRIR
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1258-2024·2024-05-29

    Marketside Brioche Rolls recalled for undeclared soy lecithin

    Marketside Brioche Rolls may contain undeclared soy lecithin, posing a risk to consumers with soy allergies. Consumers should not eat this product if they have a soy allergy.

    Product
    Marketside Brioche Rolls, Authentic French Recipe, Net Wt. (.88 OZ (280g)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1263-2024·2024-05-29

    Aldi Macaroni Salad Mislabeled as Coleslaw; Contains Undeclared Wheat

    Aldi macaroni salad products are mislabeled with a coleslaw ingredient statement that does not declare wheat. Consumers with wheat allergies could experience serious allergic reactions if they consume the product.

    Product
    Product is MACARONI Salad, but the bottom container is mislabeled with the ingredients statement for COLESLAW. Product is refrigerated and packaged in a clear square container with 3 applied labels with a clear lid. Net Wt: 32oz. (2lbs) 907 g. There are 6 packages per case. Dist
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1257-2024·2024-05-29

    Mucci's Tiramisu Italian Dessert Recalled Due to Undeclared Milk

    Mucci Food Products, Ltd. is recalling Tiramisu Italian Dessert due to undeclared milk and incomplete allergen labeling. Consumers with milk allergies are at risk.

    Product
    Mucci Food Products, Ltd. Tiramisu Italian Dessert, 2, 4.25 lb trays per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1875-2024·2024-05-29

    Merit Medical Guide Sheath Roadster Recalled for Incorrect Dilator Sizing

    Merit Medical is recalling Prelude Guide Sheath Roadster devices because some sheaths labeled as .018 dilators may actually contain .038 dilators, creating a risk of using incorrectly-sized medical devices.

    Product
    Prelude Guide Sheath Roadster, REF PG6F45S018, 6F 0.087" (2.2 mm), 45 cm, STERILE EO, RX ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1249-2024·2024-05-29

    Price Chopper Fat Free Cottage Cheese with Pineapple Recalled for Undeclared Sugar

    HP Hood is recalling Price Chopper Fat Free Cottage Cheese with Pineapple 16oz tubs due to undeclared sugar. Affected products have Item # 54267 and specific production dates in May 2024.

    Product
    Price Chopper Fat Free Cottage Cheese with Pineapple Added 16oz plastic tub.
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·24V357000·2024-05-21

    Vermeer Recalls BC900XL Trailers Due to Incorrect Manual Torque Values

    Vermeer is recalling 2015-2022 BC900XL brush chipper trailers because the service manuals list incorrect lug nut torque values, which could lead to wheel detachment.

    Product
    VERMEER — VERMEER BC900XL
    Category
    Vehicle
    Distribution
    Distributed nationwide