The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 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 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.

5076–5100 of 9610

  • HighFDA (Devices)·Z-0729-2017·2016-12-21

    Merge Cardio software recalled for potential report matching errors

    Merge Healthcare is recalling Merge Cardio software versions 8.30.0 through 10.1.1 because images sent without an order may be matched to the wrong accession number.

    Product
    Merge Cardio software. Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or optical characte
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0723-2017·2016-12-21

    Request Foods Recalls Cheese Manicotti for Undeclared Eggs

    Request Foods Inc. is recalling GFS Cheese Manicotti in tomato sauce due to undeclared eggs. The product was distributed in Michigan, Ohio, Florida, and Kentucky.

    Product
    GFS Cheese Manicotti in tomato sauce. retail 68 oz. pan. 4 retail units per case
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0740-2017·2016-12-21

    BD Recalls Spinal Anesthesia Trays Due to Incorrect Labeling

    Becton Dickinson is recalling 4,500 BD Spinal Anesthesia Trays because a small number were incorrectly labeled as Epidural Trays.

    Product
    BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is intended for use by professional anesthesiologists to perform the spinal anesthesia procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0757-2017·2016-12-21

    Pentax Ultrasound Video Bronchoscope Recalled for Incorrect Instructions

    Pentax of America Inc. is recalling 113 Ultrasound Video Bronchoscopes because they shipped with outdated instructions for use.

    Product
    Ultrasound Video Bronchoscope The EB-1970UK, Ultrasound Video Bronchoscope, is intended to provide optical visualization of, ultrasonic visualization of, and therapeutic access to, the Pulmonary Track including but not restricted to organs, tissues, and subsystem: Nasal Passage
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0722-2017·2016-12-21

    Wegmans Milk Chocolate Covered Pretzels Recalled for Incorrect Labeling

    First Source, LLC is recalling Wegmans Milk Chocolate Covered Pretzels because the rear label is incorrect and lacks allergen declarations.

    Product
    Wegmans Milk Chocolate Covered Pretzels, NET WT 9.5 OZ (269g)
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0749-2017·2016-12-21

    Ulthera Recalls Cellfina Prep Packs Due to Non-Sterile Vacuum Tube

    Ulthera Inc is recalling Cellfina Prep Packs because they contain a non-sterile vacuum tube, while the instructions describe using a sterile tube.

    Product
    Cellfina Prep Pack, Part No. CP1
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0748-2017·2016-12-21

    Ellman Minor Surgery Bipolar Cable Recalled for Mismatched Expiration Dates

    Ellman International is recalling 370 boxes of Minor Surgery Bipolar Cables because the expiration dates on the outer boxes and individual pouches do not match.

    Product
    ellman A CYNOSURE COMPANY Minor Surgery Bipolar Cable, Contents: Five (5) Disposable Bipolar Cables,STERILE The Minor Surgery Bipolar Cable is an accessory that is used to connect the bipolar handpieces to the RF generator for electrosurgical procedures that require the bipolar
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Food)·F-0683-2017·2016-12-21

    Galliker's Lemon Iced Tea Recalled for Missing Pasteurization Documentation

    Galliker Dairy Co. is recalling 2,851 gallon jugs of lemon iced tea because the products were labeled as pasteurized without legal documentation to support the claim.

    Product
    Galliker's Lemon Iced Tea Flavored, 1 GAL and Galliker's Lemon Flavored Iced Tea, 1/2 GAL
    Category
    Food
    Distribution
    3 states
  • LowFDA (Drugs)·D-0205-2017·2016-12-21

    Jubilant Cadista Recalls Methylprednisolone Tablets Due to Incorrect Expiration Date Labeling

    Jubilant Cadista Pharmaceuticals is recalling 1,512 bottles of Methylprednisolone Tablets, USP, 16 mg, because the expiration date is printed incorrectly as 02/0218 instead of 02/2018.

    Product
    Methylprednisolone Tablets, USP, 16 mg, 50-count bottles, Rx only, Manufactured by Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-003-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·118-2016·2016-12-15

    R&R Provision Recalls Breaded Veal Products Due to Undeclared Allergens

    R&R Provision Company is recalling approximately 23,040 pounds of breaded veal products because they contain undeclared whey and nonfat milk.

    Product
    Schiff's Food Service, Inc., DBA R&R Provision Company — R&R Provision Company Inc. Recalls Breaded Veal Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0608-2017·2016-12-14

    Popcorn Shoppe Popcorn Balls Recalled for Undeclared Allergens

    The Popcorn Shoppe is recalling Popcorn Balls because the labels failed to declare milk, soy, and Yellow #5.

    Product
    The Popcorn Shoppe Popcorn Balls (4) 5 oz balls, sold under the brand names of Olde Tyme Recipe, Edwards Orchards & Edwards Orchards West.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0672-2017·2016-12-14

    Mondelez Recalls Oreo Fudge Creme Cookies for Undeclared Milk Allergen

    Mondelez Global LLC is recalling Oreo Fudge Creme cookies (Original and Mint varieties) because milk is not declared on the ingredient list.

    Product
    Nabisco Oreo Fudge Creme Mint Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026967
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0671-2017·2016-12-14

    Mondelez Recalls Oreo Fudge Creme Cookies for Undeclared Milk Allergen

    Mondelez is recalling Oreo Fudge Creme cookies because milk is not listed on the ingredient label.

    Product
    Nabisco Oreo Fudge Creme Original Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026943
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0617-2017·2016-12-14

    Meijer Potato Chips Recalled for Undeclared Milk and Soy Allergens

    Shearers Foods is recalling Meijer brand No Salt Added Original Kettle Cooked Potato Chips due to undeclared milk and soy allergens.

    Product
    Meijer brand No Salt Added Original Kettle Cooked Potato Chips, 8.5oz bag. 15 bags per case.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0677-2017·2016-12-14

    Field Day Organic Ranch Dressing Recalled for Undeclared Milk and Egg Allergens

    Drews LLC is recalling Field Day Organic Ranch Dressing because some bottles have incorrect back labels that fail to list milk and egg as allergens.

    Product
    Field Day Organic Ranch Dressing packaged in an 8 fl. oz. glass bottle, UPC #042563600242. The lot code is located on the back of the bottle above the label. Specifically, the front label of the affected product is correctly labeled Field Day Organic Ranch Dressing, 8 fl oz. The
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0614-2017·2016-12-14

    Handy Seafood Recalls Blue Crab Cake Mini for Undeclared Allergens

    Handy Seafood is recalling Blue Crab Cake Mini products because milk and anchovies were not declared in the allergen statement on the packaging.

    Product
    Handy Seafood, Blue Crab Cake Mini, Mini Crab Cakes, 0.5oz per Cake/12 Cakes per Tray, Skin Packed Tray, 12 Trays per Case, 2 Year Shelf Life, Best By Nov 9, 2018.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0562-2017·2016-12-14

    SSI-GoPicnic Turkey and Cheese Snacks Recalled for Gluten Mislabeling

    SSI-GoPicnic LLC is recalling 1,584 cartons of Turkey Slices & Cheddar Cheese snacks labeled gluten-free because they contain wheat gluten.

    Product
    GoPicnic Turkey Slices & Cheddar Cheese; 4 Individually Packed Snacks; GLUTEN FREE; Best by: 31 JAN 2017
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0709-2017·2016-12-14

    BioFlo PICC Nursing Kits Recalled for Incorrect Glove Expiration Dates

    Navilyst is recalling BioFlo PICC Maximal Barrier Nursing Kits because the included sterile gloves have incorrect expiration dates.

    Product
    BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit - 1) UPN # H965750121/Catalog No: 5018265, 2) UPN # H965750131/Catalog No:5024787, 3) UPN # H965750141/Catalog No: 5024787, 4) UPN # H965750241/Catalog No: 5020644, 5) UPN # H965750325/Catalog No: 5026458, 6) UPN #
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0710-2017·2016-12-14

    BioFlo PICC Nursing Kits Recalled for Incorrect Glove Expiration Dates

    Angiodynamics is recalling BioFlo PICC Maximal Barrier Nursing Kits because included sterile gloves have incorrect expiration dates.

    Product
    BioFlo PICC with ENDEXO and PASV Valve Technology Maximal Barrier Nursing Kit - UPN # H965750191/Catalog No:75-019 The BioFlo PICCs with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous system for intravenous therapy,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0708-2017·2016-12-14

    Navilyst Recalls Xcela PICC Kits Due to Incorrect Glove Expiration Dates

    Navilyst Medical is recalling Xcela Power Injectable PICC Maximal Barrier Nursing Kits because included sterile gloves have incorrect expiration dates.

    Product
    Xcela Power Injectable PICC Maximal Barrier Nursing Kit The Maximal Barrier Nursing Kits are Tandem Pack Convenience Kits packaged with a NMI PICC and accessories. The Xcela Power Injectable PICC is indicated for short or long-term peripheral access to the central venous system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0561-2017·2016-12-14

    Coca-Cola Recalls Dr. Pepper Cherry Cans for Undeclared Corn Syrup

    The Coca-Cola Company is recalling 1,020 cases of Dr. Pepper Cherry 12oz 12-packs in California due to undeclared high-fructose corn syrup.

    Product
    Dr. Pepper Cherry, 12oz (12 pack cans), Manufactured under the authority of Doctor Pepper Company, 5301 Legacy Drive, Plano, TX.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0675-2017·2016-12-14

    A&W Cream Soda Recalled for Caffeine Presence Despite Labeling

    Chesterman Co is recalling A&W Cream Soda, 20 FL OZ, Caffeine Free, because testing revealed the presence of caffeine despite the product being labeled as caffeine-free.

    Product
    A&W Cream Soda, 20 FL OZ, Caffeine Free
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0704-2017·2016-12-14

    Ultradent Recalls UltraSeal XT Plus Clear Refill Due to Labeling Error

    Ultradent Products, Inc. is recalling 31 units of UltraSeal XT Plus Clear Refill, Lot BD79T, because the package was mislabeled with an incorrect part number.

    Product
    UltraSeal XT Plus Clear Refill. The package contains 4x 1.2 ml UltraSeal XT Plus. Product Usage: The UltraSeal XT Plus is used for prophylactic sealing of pits and fissures. It may also be used for micro restorative or initial layer of composite restorations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0714-2017·2016-12-14

    Angiodynamics Recalls PICC Catheters Due to Stylet Diameter Labeling Error

    Angiodynamics Inc. is recalling specific PICC catheters because the stylet diameter may differ from the label, potentially causing stiffening.

    Product
    Peripherally Inserted Central Catheters (PICC), UPN H965750141, Catalog # 75-014 The Maximal Barrier Nursing Kits are Tandem Pack Convenience Kits packaged with a NMI PICC and accessories. The BioFlo PICC with ENDEXO Technology and BioFlo PICC with ENDEXO and PASV Valve Technolo
    Category
    Medical Device
    Distribution
    Distributed nationwide