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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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

1526–1550 of 26155

  • HighFDA (Food)·H-0575-2026·2026-03-25

    Dreamland's Zaatar Chickpea Salad recalled for undeclared allergens

    Dreamland Inc is recalling Zaatar Chickpea Salad distributed to Haggen stores in Washington because it contains undeclared sesame, soy, and wheat allergens not listed on the label.

    Product
    Dreamland's Zaatar Chickpea Salad is packaged in poly bags with a generic label which declares "chickpeas, cumin, zataar, turmeric, dill, onion, garlic, parsley". Dreamland distributed bulk cases (2/5lbs. bags per case) to Haggen store. Bulk 5lbs. bags were not sold directly to c
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0579-2026·2026-03-25

    Clover Sonoma Cottage Cheese Recalled for Potential Under-Pasteurization

    Clover Sonoma low-fat cottage cheese (16 oz and 32 oz sizes) is being recalled due to potential under-pasteurization from a broken pasteurizer seal. The product may not be safe for consumption.

    Product
    CLOVER SONOMA COTTAGE CHEESE LOW FAT 2% MILKFAT NET WT 16OZ UPC 0 70852 54400 7 & 32OZ UPC 0 70852 54200 3 DISTRIBUTED BY: CLOVER-STORNETTA FARMS LLC PETALUMA, CA 94952
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·H-0571-2026·2026-03-25

    Miss Vickies Spicy Dill Pickle chips recalled for undeclared milk allergen

    Frito-Lay North America is recalling Miss Vickies Spicy Dill Pickle 8 oz bags that contain undeclared milk allergen. Affected products were distributed in Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, and Texas.

    Product
    Miss Vickies Spicy Dill Pickle; 8 oz bag
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0570-2026·2026-03-25

    Simply Nature Spinach Bites recalled for possible rodent hair contamination

    Dr. Praeger's Sensible Foods Inc. is recalling Simply Nature Spinach Bites (12 oz) due to the possibility of rodent hair contamination. The affected product was distributed to Maryland and Pennsylvania.

    Product
    Simply Nature, Spinach Bites, 12 oz retail unit, Plastic wrapped bites inside of a retail box. Keep Frozen.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0407-2026·2026-03-25

    Prescription Eye Drops Recalled for Lack of Sterility Assurance

    Apotex Corp. is recalling brimonidine tartrate/timolol maleate ophthalmic solution nationwide due to lack of sterility assurance. The recall affects 107,136 vials across two lots.

    Product
    BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION — BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION (BRIMONIDINE TARTRATE AND TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0390-2026·2026-03-25

    Children's Ibuprofen Suspension Recalled for Foreign Particle Contamination

    Strides Pharma is recalling Children's Ibuprofen Oral Suspension due to the presence of gel-like masses and black particles found in the product. Affected lots 7261973A and 7261974A should not be used.

    Product
    IBUPROFEN — IBUPROFEN (IBUPROFEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0398-2026·2026-03-25

    Dexamethasone Sodium Phosphate Injection Recalled for Failed Impurity Specifications

    Somerset Therapeutics LLC recalled 62,190 vials of Dexamethasone Sodium Phosphate Injection due to out-of-specification impurities detected during stability testing. The affected lot was found to contain elevated levels of certain degradation products at product expiry.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1572-2026·2026-03-25

    MICS3 Angled Sagittal Saw Attachment external screws may loosen during use

    Howmedica Osteonics' MICS3 Angled Sagittal Saw Attachment screws may loosen and detach during use. The recall affects approximately 1,098 units distributed nationwide and internationally.

    Product
    MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1581-2026·2026-03-25

    Leksell Gamma Knife Radiosurgery Systems: Adapter Misalignment Risk Recall

    Elekta recalls Leksell Gamma Knife radiosurgery systems where the adapter may not be properly aligned or locked in place, potentially affecting treatment delivery accuracy.

    Product
    Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell Gamma Knife¿ Elekta Esprit Leksell Gamma Knife¿ (available models Elekta Esprit, Icon", and Perfexion") is a radiosurgery system for use in the stereot
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1582-2026·2026-03-25

    ConvaTec EsteemBody Drainable Pouch may leak due to manufacturing defect

    ConvaTec EsteemBody Drainable Pouches may leak due to a manufacturing defect. The affected products (Ref 423643, 10-45mm, UDI 00768455221264, lots 5K00011 and 5K00714) are distributed worldwide.

    Product
    Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1580-2026·2026-03-25

    Pediatric Crib Recall: Missing Safety Warning Labels on Access Doors

    Stryker is recalling Cub Pediatric Cribs (Model FL19H) due to missing access door warning labels that could affect proper equipment use.

    Product
    Cub Pediatric Crib, Model FL19H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1571-2026·2026-03-25

    Medical device software cybersecurity vulnerability exposes user credentials

    Centricity Universal Viewer Software has a cybersecurity vulnerability that may expose user login credentials on workstations. Unauthorized individuals could impact system availability or manipulate medical data.

    Product
    Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1573-2026·2026-03-25

    Welch Allyn VS100 Vision Screener display flickering may trigger seizures

    The Welch Allyn Spot Vision Screener VS100 may display flickering due to a software issue. Flickering light exposure could trigger photosensitive seizures in susceptible individuals.

    Product
    Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit pe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·26328·2026-03-19

    Wagner 900 Series Power Steamers Recalled Due to Burn Hazard

    Wagner Spray Tech recalled about 700,000 power steamers because the hose and nozzle can get excessively hot, causing burns. Over 50 consumers reported burn injuries, many first- or second-degree.

    Product
    Wagner 900 Series Power Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26333·2026-03-19

    Frigidaire Gas Ranges Recalled for Delayed Ignition Burn Hazard

    Electrolux is recalling about 174,800 Frigidaire gas ranges for a delayed oven ignition hazard that has caused 30 reported burn injuries. Free repairs are available.

    Product
    Frigidaire Gas Ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26329·2026-03-19

    Tainoki Fine Furniture Recalls Office Chairs Due to Fall Hazard

    Tainoki Fine Furniture is recalling about 2,200 swivel office chairs sold at HomeGoods because the chair base can bend and cause a fall hazard. No injuries have been reported.

    Product
    Swivel Office Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26332·2026-03-19

    Goregent Infant Walkers Recalled Due to Fall Hazard Risk

    Goregent infant walkers sold on Amazon are recalled because they can fit through standard doorways and fail to stop at stairs, creating a fall hazard. No injuries have been reported.

    Product
    Goregent Infant Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26330·2026-03-19

    Specialized Turbo Como SL Electric Bicycles Recalled for Fork Failure Fall Hazard

    Specialized Turbo Como SL electric bicycles' fork steerer tubes can develop fatigue cracks leading to failure and fall risk. About 5,720 units sold March 2021–January 2026 are affected.

    Product
    Specialized Turbo Como SL 4.0 & 5.0 Bicycle Forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26335·2026-03-19

    Adult Bicycle Helmets Recalled for Failing Safety Standards

    Approximately 200 Aisstxoer adult bicycle helmets sold on Amazon violate mandatory safety standards and may fail to protect against head injury. Consumers should stop using them immediately and contact the seller for a refund.

    Product
    Aisstxoer Adult Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26334·2026-03-19

    Amazon Basics Camping Folding Pocket Knives Recalled for Laceration Hazard

    Amazon is recalling about 2,840 Camping Folding Pocket Knives because the blade's folding mechanism can fail to stay closed, posing a laceration hazard. No injuries have been reported.

    Product
    Amazon Basics Camping Folding Pocket Knives
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0564-2026·2026-03-18

    Made Fresh Salads Sundried Tomato Cream Cheese Recalled for Listeria Contamination

    Made Fresh Salads brand Sundried Tomato Cream Cheese (5 lb tubs) is being recalled because it may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact the manufacturer or their retailer.

    Product
    Made Fresh Salads brand Sundried Tomato Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0559-2026·2026-03-18

    Made Fresh Salads Jalapeno Cream Cheese Recalled for Listeria Risk

    Made Fresh Salads brand Jalapeno Cream Cheese in 5 lb tubs is being recalled due to potential Listeria monocytogenes contamination. All products with expiration dates through February 27, 2026 sold in New York are affected.

    Product
    Made Fresh Salads brand Jalapeno Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0566-2026·2026-03-18

    Made Fresh Salads Walnut Raisin Cream Cheese Listeria contamination recall

    Made Fresh Salads brand Walnut Raisin Cream Cheese in 5 lb tubs is being recalled because it may be contaminated with Listeria monocytogenes. The recall affects products distributed in New York with expiration dates through 2/27/2026.

    Product
    Made Fresh Salads brand Walnut Raisin Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0568-2026·2026-03-18

    Made Fresh Salads Tofu Whipped product recall due to Listeria contamination

    Made Fresh Salads brand Tofu Whipped in 5 lb tubs is being recalled because products may be contaminated with Listeria monocytogenes. The recalled product was distributed in New York.

    Product
    Made Fresh Salads brand Tofu Whipped; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states