The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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14926–14950 of 27762

  • HighFDA (Devices)·Z-0570-2024·2023-12-27

    Biomet Recalls Hip Implant Adapter Due to Wrong Specification in Packaging

    Biomet is recalling a hip implant adapter lot due to incorrect packaging containing the wrong adapter specification. The mismatch could result in incorrect implant selection during surgery if not detected before use.

    Product
    Biolox Ceramic Option Head Zimmer 12/14 40mm +0, Item Number 00-8777-040-02
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Drugs)·D-0155-2024·2023-12-27

    Nystatin Powder Recall Due to Incorrect Assay Strength on Label

    Fagron, Inc. is recalling 46 containers of Nystatin 500 MU bulk powder used for prescription compounding due to an incorrect assay value on the product label. The mislabeled strength could affect proper compounding of patient medications.

    Product
    NYSTATIN 500 MU, Activity (as is): 6482 Units/mg, bulk powder container, Rx Only, For Prescription Compounding, Fagron, Inc. - 2400 Pilot Knob Rd. St Paul, MN 55120. NDC 51552-0041-3, Bar code 3 51552 00413 9
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0604-2024·2023-12-27

    Abbott Hematology Analyzers Recalled for Unlabeled Latex Component

    Abbott CELL-DYN Ruby and Sapphire hematology analyzers contain latex that is not labeled on the device, posing a risk to users with latex allergies. The recall affects 670 devices distributed across 33 states, Puerto Rico, and Brazil.

    Product
    Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN Sapphire, Model CD Sapphire, list number 08H00-01. Multi-parameter, automated hematology analyzer.
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Devices)·Z-0583-2024·2023-12-27

    Exactech Optetrak Logic Knee System Recalled for Vacuum Bag Failure

    Exactech is recalling certain Optetrak Logic Knee System devices due to loss of vacuum in the inner-most vacuum bag. The company has received three complaints involving four affected devices.

    Product
    Exactech Optetrak Logic Knee System, Catalog Numbers: a) 02-012-47-3011, b) 02-012-47-5009, c) 02-012-47-5011, d) 02-012-65-3013
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Drugs)·D-0156-2024·2023-12-27

    Nystatin Bulk Powder Recalled Due to Incorrect Label Strength

    Fagron Inc. is recalling 9 containers of Nystatin 2 BU bulk powder because the assay value on the label is incorrect, which could affect dosing accuracy in pharmacy compounding.

    Product
    NYSTATIN 2 BU, Activity (as is): 6482 Units/mg, bulk powder container, Rx Only, For Prescription Compounding, Fagron, Inc. - 2400 Pilot Knob Rd. St Paul, MN 55120. NDC 51552-0041-4, Bar code 3 51552 00414 6
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0587-2024·2023-12-27

    Exactech Vantage Ankle System Recalled Due to Vacuum Loss

    Exactech is recalling two catalog numbers of Vantage Ankle System devices due to loss of vacuum in the inner-most vacuum bag. Three complaints have been received relating to four affected devices.

    Product
    Exactech Vantage Ankle System, Catalog Numbers: a) 350-21-04, b) 350-22-03
    Category
    Medical Device
    Distribution
    16 states
  • SevereCPSC·24064·2023-12-21

    Brandline HEAO 4-in-1 High Chairs Recalled for Suffocation and Laceration Risks

    Brandline is recalling about 820 HEAO 4-in-1 high chairs sold on Amazon from November 2022 through September 2023 because they pose suffocation, finger laceration, and entrapment hazards. One child has suffered a laceration requiring medical attention.

    Product
    HEAO 4-in-1 High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24065·2023-12-21

    Hover-1 Helix Hoverboards Recalled Due to Fire Hazard

    About 25,000 Hover-1 Helix hoverboards in Camouflage and Galaxy colors are recalled because their lithium-ion batteries can overheat and catch fire. Three fires have been reported, along with smoke inhalation injuries and property damage.

    Product
    Hover-1 Helix hoverboards (Camouflage and Galaxy colors only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24066·2023-12-21

    FeraDyne Outdoors Recalls Rhino Tree Stands Due to Fall Hazard

    FeraDyne Outdoors is recalling about 50,000 Rhino Tree Stands because the safety harness stitching can rip, creating a fall hazard. No injuries have been reported.

    Product
    Rhino Tree Stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24067·2023-12-21

    Klein Tools and Blackfire Portable Power Stations Recalled for Fire and Burn Hazards

    Klein Tools and Blackfire portable rechargeable power stations are being recalled because their internal inverter boards can overheat, creating fire and burn hazards. Consumers should stop using the units and return them to their original point of purchase.

    Product
    Portable Rechargeable Power Stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24732·2023-12-21

    Pella Architect Series Casement Windows Recalled for Detachment Injury Hazard

    Pella Corporation is recalling approximately 12,000 Architect Series Casement Windows because the window sash can detach from the frame and fall, creating an injury risk. The company has received one report of detachment but no injuries have been reported.

    Product
    Pella Architect Series Casement Windows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24737·2023-12-21

    Litti City and Litti Pritti Dress-Up Playsets and Prextex Slime Eggs Recalled for Phthalate and Lead Violations

    Litti City Premier Doctor and Teacher Purse playsets, Litti Pritti Stylist Handbag set, and Prextex Slime Eggs are recalled for containing phthalates and lead exceeding federal safety standards. No injuries have been reported.

    Product
    Litti City Premier Doctor Playset and Teacher Purse Set, Litti Pritti Stylist Handbag Set, and Prextex Slime Eggs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0599-2024·2023-12-20

    Maggi 2-Minute Noodles Recalled for Undeclared Peanut Allergen

    Maggi 2-Minute Noodles sold in California are being recalled for undeclared peanut allergen. Consumers with peanut allergies should not consume this product.

    Product
    Maggi 2-Minute Noodles; 560g (12 packets per case); plastic pouch; store in a cool dry place
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0515-2024·2023-12-20

    Wilcox Ice Cream Chocolate Recalled Due to Listeria Contamination

    Wilcox SUPER PREMIUM Chocolate ice cream in 1.5 QT and Pint sizes is recalled for potential Listeria monocytogenes contamination. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York with Best By/Sell By dates from 9/13/24 to 11/14/24.

    Product
    Wilcox SUPER PREMIUM Chocolate; 1.5 QT (UPC 04372601502) and Pint (UPC 04372601602)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0526-2024·2023-12-20

    Wilcox Ice Cream Bars Recalled Due to Listeria Contamination Risk

    Wilcox Ice Cream Bars (Espresso) sold in VT, NH, MA, and NY may be contaminated with Listeria monocytogenes. Consumers should not consume the product.

    Product
    Wilcox Ice Cream Bar (Dairy Based) - Espresso (UPC 043726005072)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0587-2024·2023-12-20

    Mixed Fruit Products Containing Cantaloupe Recalled for Salmonella

    Cut Fruit Express is recalling mixed fruit products containing cantaloupe that may be contaminated with Salmonella. The products were distributed in Illinois, Minnesota, and Wisconsin.

    Product
    Mixed Fruit Products that contain Cantaloupe, Honeydew, Pineapple, and Watermelon, Identified with the following Item ID and Description. 4702 Four Fruit CHPW
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0519-2024·2023-12-20

    Wilcox Super Java ice cream recalled due to Listeria contamination risk

    Wilcox SUPER PREMIUM Super Java ice cream (1.5 QT and Pint) may be contaminated with Listeria. Affected products were distributed in VT, NH, MA, and NY with Best By/Sell By dates from 9/13/24 to 11/14/24.

    Product
    Wilcox SUPER PREMIUM Super Java; 1.5 QT (UPC 04372601516) and Pint (UPC 04372601616)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0579-2024·2023-12-20

    Cantaloupe Recall: Salmonella Risk in Malichita Whole Cantaloupe

    PACIFIC TRELLIS FRUIT, LLC is recalling Malichita brand whole cantaloupes in 9-count and 12-count packages due to potential Salmonella contamination. The recall affects 4,872 cases distributed in Wisconsin, Oklahoma, Illinois, Texas, California, and Canada.

    Product
    Malichita brand Whole Cantaloupe 9 count and 12 count
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0524-2024·2023-12-20

    Wilcox Ice Cream Bar Recalled for Possible Listeria Contamination

    Wilcox Ice Cream Bar (Dairy Based) - Vanilla may be contaminated with Listeria monocytogenes. Consumers with best-by dates from September 15, 2024, through November 14, 2024, should not consume the product.

    Product
    Wilcox Ice Cream Bar (Dairy Based) - Vanilla; UPC 043726005041
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0537-2024·2023-12-20

    Wilcox Premium Mint Chocolate Chip Ice Cream Recalled for Listeria Contamination

    Wilcox Premium Mint Chocolate Chip ice cream sold in VT, NH, MA, and NY has been recalled due to potential Listeria monocytogenes contamination. Consumers should discard the product or return it to the point of purchase.

    Product
    Wilcox Premium Mint Chocolate Chip in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0511-2024·2023-12-20

    Wilcox Premium Sea Salt Caramel Ice Cream Recalled for Listeria Contamination

    Wilcox Premium Sea Salt Caramel ice cream is being recalled for potential Listeria monocytogenes contamination. Affected products with best-by dates of 9/14/24 to 11/14/24 were distributed in VT, NH, MA, and NY.

    Product
    Wilcox Premium Sea Salt Caramel; 4 oz Cup; UPC 04372600404; Wilcox Premium Sea Salt Caramel in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0592-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies found in gift baskets due to undeclared tree nuts. The cookies were distributed nationwide to all U.S. states.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #343 Brownie, Cookie & Cake Assortment
    Category
    Food
    Distribution
    49 states
  • CriticalFDA (Food)·F-0525-2024·2023-12-20

    Wilcox Ice Cream Bar Recalled for Potential Listeria Contamination

    Wilcox Ice Cream Bar (Black Raspberry) is being recalled due to potential Listeria monocytogenes contamination. The affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Wilcox Ice Cream Bar (Dairy Based) Black Raspberry (UPC 043726005065)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0516-2024·2023-12-20

    Wilcox Ice Cream Recalls Maple Cream for Potential Listeria Contamination

    Wilcox Ice Cream is recalling Maple Cream in 1.5 quart and pint sizes due to potential Listeria monocytogenes contamination. The affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York with best-by dates from September 13 to November 14, 2024.

    Product
    Wilcox SUPER PREMIUM Maple Cream; 1.5 QT (UPC 04372601510) and Pint (UPC 04372601610)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0596-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. recalls Acorn Raspberry Creme Filled Cookies from gift baskets for undeclared tree nuts. Approximately 4,875 cookies across 1,168 gift boxes were distributed nationwide. Consumers with tree nut allergies should not consume this product.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #926 Tis The Season Bakery Gift Box
    Category
    Food
    Distribution
    49 states