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.

4501–4525 of 9607

  • LowFDA (Drugs)·D-0906-2017·2017-06-21

    Pharmedium Recalls 216 Bags of Potassium Chloride with Incorrect Volume Labeling

    Pharmedium Services, LLC is recalling 216 bags of Potassium Chloride in 0.9% Sodium Chloride because the product labels incorrectly state a volume of 115.00 mL instead of the actual 100.00 mL.

    Product
    Potassium CHLORide added to 0.9% Sodium Chloride, 30mEq 100 mL Bag, Service Code 2K5824, NDC# 61553-0824-48, Total Volume 100.00 mL incorrectly labeled as 115.00 mL, Rx Only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 38141
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2587-2017·2017-06-21

    Teleflex Recalls Sheridan Intubating Stylets Due to Incorrect Size Labeling

    Teleflex Medical is recalling Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets because the product size listed on the labeling is incorrect.

    Product
    Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are coated with a blue PVC or polypropylene outer covering and are designed to be placed inside an endotracheal tube to obtain a desired sh
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowNHTSA·17V387000·2017-06-20

    KZRV Recalls 2018 Recreational Trailers Due to Missing Certification Date

    KZRV is recalling 2018 recreational trailers because the Federal Certification label lacks the manufacturing date, potentially preventing owners from identifying other safety recalls.

    Product
    KZRV — KZRV VENOM, SPORTSMEN SPORTSTER, SPREE, SPORT TREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·072-2017·2017-06-14

    Golden Platter Foods Recalls Poultry and Beef Products for Undeclared Milk

    Golden Platter Foods Inc. is recalling approximately 31,662 pounds of ready-to-eat poultry and beef products due to misbranding and undeclared milk, a known allergen.

    Product
    Golden Platter Foods Inc. — Golden Platter Foods Inc. Recalls Poultry and Beef Products
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2334-2017·2017-06-14

    Whole Foods Oatmeal Chocolate Chip Cookies Recalled for Undeclared Walnuts

    Whole Foods Market is recalling Oatmeal Chocolate Chip Cookies due to undeclared walnuts, a major food allergen.

    Product
    Oatmeal Chocolate Chip Cookies, 18pk, NET WT. 0 lb 10 oz (283 g), Dist. by Whole Foods Market, 1105 N. Lamar, Austin, TX 78703 USPC 0247181 004992
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2306-2017·2017-06-14

    Arrow International Recalls Two-Lumen Hemodialysis Catheterization Kits

    Arrow International Inc is recalling specific lots of two-lumen hemodialysis catheterization kits due to a Class II medical device recall.

    Product
    Two-Lumen Hemodialysis Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions for High Volume Infusions The Arrow(r) CVC is indicated to provide short-term ( < 30 days) central venous access for treatment of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2308-2017·2017-06-14

    Arrow International Recalls Hemodialysis Catheterization Kits

    Arrow International Inc. is recalling ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kits due to a Class II recall.

    Product
    ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions The Arrow(r) CVC is indicated to provide short-term ( < 30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2319-2017·2017-06-14

    California Sun Dry Sun-Dried Tomato Pesto Recalled for Undeclared Allergens

    California Sun Dry Foods is recalling Sun-Dried Tomato Pesto because the label failed to declare almonds and milk.

    Product
    California Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar; Ingredients (incorrect) Garlic, Canola oil, sundried tomatoes (preserved with sulfating agents) water, sola oil, spices, onion, salt, citric acid,, soy lecithin. Partially processed with Genetic En
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·F-2327-2017·2017-06-14

    Choice Northwest Recalls Paradise Deli Hazelnut Cake for Undeclared Soy

    Choice Northwest is recalling Paradise Deli brand Hazelnut Cake because the product contains undeclared soy lecithin, a major food allergen.

    Product
    Hazelnut Cake, Paradise Deli brand, net wt. 15 oz., UPC 0 31619 10201 4. The label is read in parts: "***Contains: Oregon grown hazelnuts, cane sugar, organic unbleached wheat flour, fresh eggs, sea salt, pure vanilla***PARADISE DELI - PO Box 22411, Eugene, OR 97402 *** 925 37
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2328-2017·2017-06-14

    Parade Deli Cake Recalled for Undeclared Soy Lecithin

    Choice Northwest is recalling Paradise Deli brand Love Your Heart Cake because it contains undeclared soy lecithin. The product was distributed in Oregon.

    Product
    Love Your Heart Cake, Paradise Deli brand, Net Wt. 14 oz., UPC 0 31619 40402 6. The label is read in parts: "***Contains: Fresh apples, fresh carrots, organic unbleached wheat flour, organic cane sugar, Oregon grown hazelnuts, raisins, cinnamon, baking soad, and baking powder*
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2312-2017·2017-06-14

    Cook Medical Recalls Willscher Vas Reapproximator Plates Due to Reprocessing Instructions

    Cook Medical is voluntarily recalling Willscher Vas Reapproximator Plates because the reprocessing instructions lack sufficient detail for cleaning, disinfection, and sterilization.

    Product
    Willscher Vas Reapproximator Plate, Surgical Instrument, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to stabilize the vas ends during microscopic vasovasostomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2315-2017·2017-06-14

    Cook Medical Recalls LapSac Introducer Sets Due to Insufficient Reprocessing Instructions

    Cook Medical is voluntarily recalling 335 LapSac Introducer Sets because the provided reprocessing instructions lack sufficient detail for proper cleaning, disinfection, and sterilization.

    Product
    LapSac Introducer Set, Bag, Extraction, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to aid in the introduction of a LapSac during endoscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2311-2017·2017-06-14

    Cook Medical Recalls Willscher Vas Skewers Due to Insufficient Reprocessing Instructions

    Cook Medical is voluntarily recalling Willscher Vas Skewers because the provided instructions do not contain sufficient detail for proper cleaning, disinfection, and sterilization.

    Product
    Willscher Vas Skewers, Surgical Instrument, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to stabilize the vas ends during microscopic vasovasostomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2313-2017·2017-06-14

    Cook Medical Recalls Endoscopic Curved Needles Due to Reprocessing Instruction Deficiencies

    Cook Medical is voluntarily recalling 725 units of endoscopic curved needles because the reprocessing instructions do not provide sufficient detail for proper cleaning and sterilization.

    Product
    Endoscopic Curved Needle, Surgical Needle Guide, Supplied sterilized by ethylene oxide gas in peel-open packages. Used for internal suturing under direct vision during intraabdominal endoscopic procedures. The needle driver design affords precise placement and control of stand
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2320-2017·2017-06-14

    Denali Moose Tracks Cheesecake Recalled for Incorrect Peanut Allergen Labeling

    The Father's Table, LLC is recalling Denali Original Moose Tracks Cheesecake because the rear label is for a different product and lacks a peanut allergen declaration.

    Product
    Denali "Original" Moose Tracks Cheesecake, Net Wt. 18 oz (510g). Black plastic base with clear plastic dome. Back label includes nutrition labeling for Pumpkin Swirl Cheesecake. Manufactured by The Father's Table, LLC
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2251-2017·2017-06-14

    Teleflex Recalls Pediatric Nasal Cannulas Due to Incorrect Labeling

    Teleflex Medical is recalling 1,150 Hudson RCI Pediatric Nasal Cannulas because the box label says 'Pediatric' while the insert says 'Adult'.

    Product
    Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,
    Category
    Medical Device
    Distribution
    20 states
  • LowFDA (Devices)·Z-2309-2017·2017-06-14

    Beekley Medical Mammography Skin Markers Recalled for Mislabeling

    Beekley Corporation is recalling 0-SPOT Mammography Skin Markers because they were mislabeled with A-SPOT labels. The recall affects 6,032 units distributed in the US and Canada.

    Product
    Beekley Medical 0-SPOT Mammography Skin Markers REF 652
    Category
    Medical Device
    Distribution
    9 states
  • LowFDA (Devices)·Z-2221-2017·2017-06-14

    Acumedia Urea Base Agar Recalled for Incorrect Storage Labeling

    Acumedia is recalling Urea Base Agar because the label listed an incorrect storage temperature range.

    Product
    Urea Base Agar, Acumedia PN 7226 Urea Agar Base is used with agar for the differentiation of microorganisms on the basis of urease production
    Category
    Medical Device
    Distribution
    1 state
  • CriticalUSDA FSIS·065-2017·2017-06-09

    Conagra Recalls Spaghetti and Meatball Products for Undeclared Milk Allergen

    Conagra Brands is recalling approximately 717,338 pounds of spaghetti and meatball products because they contain undeclared milk, a known allergen.

    Product
    Hometown Food Company — Conagra Brands, Inc. Recalls Spaghetti and Meatball Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2017·2017-06-08

    Maid-Rite Recalls Beef Products Due to Undeclared Milk Allergen

    Maid-Rite Specialty Foods is recalling approximately 174,000 pounds of beef products because they contain undeclared milk, a known allergen.

    Product
    Maid-Rite Specialty Foods, Inc — Maid-Rite Specialty Foods, LLC. Recalls Beef Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2289-2017·2017-06-07

    Mikawaya Recalls Mochi Ice Cream Due to Potential Peanut Allergen

    Mikawaya is recalling Mochi Ice Cream Chocolate Chocolate because it may contain Chocolate Peanut Butter Ice Cream, posing a risk to individuals with peanut allergies.

    Product
    Mikawaya Mochi Ice Cream Chocolate Chocolate, 6-1.5oz (43g) pieces, Net Wt. 9.1oz (258g), UPC 070934990609, 24 boxes/case
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2287-2017·2017-06-07

    Lyrical Foods Mushroom and Ricotta Ravioli Recalled for Missing Garlic Labeling

    Lyrical Foods is recalling Kite Hill Mushroom and Ricotta Ravioli because the ingredient statement fails to list garlic.

    Product
    Kite Hill Mushroom and Ricotta Ravioli; frozen Ravioli made with almond milk ricotta: 9 oz. package. UPC 856624004173 Owned and distributed by Lyrical Foods, Hayward, CA.
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2178-2017·2017-06-07

    AbbVie Recalls PEG Kits Due to Missing or Duplicate Components

    AbbVie is recalling 3,331 PEG kits distributed in the US and 31 other countries because they may have missing components, duplicate parts, or missing labels.

    Product
    AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2170-2017·2017-06-07

    Arrow VPS Access Kit Recalled for Missing Dressing Information

    Arrow International is recalling VPS Access Kits because they lack required information regarding the included 3M Tegaderm CHG dressing.

    Product
    Arrow(R) VPS(R) Access Kit for use with 4 and 5 Fr. Peripherally Inserted Central Venous Catheters
    Category
    Medical Device
    Distribution
    1 state