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 agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

2776–2800 of 36527

  • SevereFDA (Devices)·Z-1279-2025·2025-03-26

    Smiths Medical ProPort Implantable Port Component Separation Due to Manufacturing Defect

    Smiths Medical is recalling ProPort Plastic implantable port systems because the plastic port housing and port reservoir may separate due to a manufacturing defect. The recall affects 2,311 units distributed worldwide.

    Product
    smiths medical ProPort Plastic Venous Access System, PolyFlow Polyurethane Catheter, 1.9mm O.D. (5.8 Fr) x 1.0mm I.D., REF 21-4152-24
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0638-2025·2025-03-26

    Berry Buddies breakfast cups recalled for undeclared wheat and egg allergens

    Berry Buddies fruit-and-pancake cups are being recalled because the back label does not list wheat and eggs as allergens. People with allergies to these ingredients could have serious reactions.

    Product
    Berry Buddies; Blueberries, Mini Pancakes & Real Maple Syrup; NET WT 2.1 oz (60 g); 3-compartment non-flex plastic container with heat-sealed plastic film containing mini pancakes, blueberries, and maple syrup
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-0281-2025·2025-03-26

    Dietary Supplement Tainted with Undeclared Sildenafil and Tadalafil

    Vitality male enhancement dietary supplement recalled nationwide. Product contains undeclared prescription drugs sildenafil and tadalafil not disclosed to consumers.

    Product
    Vitality, Fast Acting Male Enhancement Product, Dietary Supplement, a) One Capsule per Packet, b) 6 capsules per bottle, Xtreme Potency.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0653-2025·2025-03-26

    Lyons Magnus chocolate shakes recalled due to potential Listeria contamination

    Two chocolate shake products from Lyons Magnus are being recalled due to potential Listeria monocytogenes contamination affecting approximately 763,250 cases distributed to healthcare facilities nationwide.

    Product
    Ready Care Chocolate Shake (4 oz), UPC 10045796017341; Imperial Chocolate Shake (4 oz), UPC 00074865926997
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0658-2025·2025-03-26

    Ready Care and Imperial Shakes Recalled for Listeria Contamination Risk

    Ready Care and Imperial Strawberry Banana Shakes are being recalled due to potential Listeria monocytogenes contamination. The affected products were distributed to long-term care facilities, hospitals, and nursing homes.

    Product
    Ready Care Strawberry Banana Shake No Sugar Added (4 oz), UPC 10045796018447; Imperial Strawberry Banana Shake No Sugar Added (4 oz), UPC 00074865987325
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0660-2025·2025-03-26

    Ready Care Chocolate Shake Plus Recalled for Potential Listeria Contamination

    Lyons Magnus LLC is recalling Ready Care Chocolate Shake Plus (4 oz) due to potential Listeria monocytogenes contamination. The recall affects 763,250 cases distributed to long-term care facilities, skilled nursing homes, and hospitals.

    Product
    Ready Care Chocolate Shake Plus (4 oz), UPC 10045796017471
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1281-2025·2025-03-26

    Smiths Medical ProPort Implantable Port Risk of Component Separation

    Smiths Medical is recalling its ProPort Plastic Implantable Ports due to a manufacturing defect that may cause the port housing and reservoir to separate, potentially compromising device function.

    Product
    smiths medical ProPort Plastic Venous Access System, PolyFlow Polyurethane Catheter, 2.6mm O.D. (7.8Fr) x 1.6mm I.D., REF 21-4155-24
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0662-2025·2025-03-26

    Ready Care Vanilla Shake Plus 4 oz Recalled for Listeria Contamination

    Lyons Magnus LLC is recalling Ready Care Vanilla Shake Plus (4 oz, UPC 10045796017549) due to potential contamination with Listeria monocytogenes. The product was distributed to hospitals, nursing homes, and long-term care facilities across the United States.

    Product
    Ready Care Vanilla Shake Plus (4 oz), UPC 10045796017549
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0655-2025·2025-03-26

    Vanilla Shake Products Recalled Due to Potential Listeria Contamination

    Lyons Magnus is recalling Ready Care and Imperial Vanilla Shake products for potential Listeria monocytogenes contamination. The affected products were distributed to healthcare facilities nationwide.

    Product
    Ready Care Vanilla Shake (4 oz), UPC 10045796017334; Imperial Vanilla Shake (4 oz), UPC 00074865926836
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0656-2025·2025-03-26

    Ready Care and Imperial Chocolate Shakes Recalled for Listeria Contamination Risk

    Lyons Magnus LLC is recalling Ready Care and Imperial Chocolate Shakes due to potential Listeria monocytogenes contamination. The recalled products were distributed nationwide to healthcare facilities and long-term care settings.

    Product
    Ready Care Chocolate Shake No Sugar Added (4 oz), UPC 10045796036335; Imperial Chocolate Shake No Sugar Added (4 oz), UPC 10734730244720
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0654-2025·2025-03-26

    Lyons Magnus Recalls Strawberry Shakes for Potential Listeria Contamination

    Lyons Magnus LLC is recalling Ready Care and Imperial Strawberry Shake products due to potential Listeria monocytogenes contamination. The recall affects 763,250 cases distributed to healthcare facilities.

    Product
    Ready Care Strawberry Shake (4 oz), UPC 10045796017358; Imperial Strawberry Shake (4 oz), UPC 00074865927017
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0661-2025·2025-03-26

    Ready Care Strawberry Shake Recalled for Potential Listeria Contamination

    Lyons Magnus LLC is recalling Ready Care Strawberry Shake Plus (4 oz) due to potential Listeria monocytogenes contamination. The affected product has been distributed to healthcare facilities nationwide.

    Product
    Ready Care Strawberry Shake Plus (4 oz), UPC 10045796017495
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·25V055000·2025-03-25

    Volvo Recalls 2023-2025 VNR Electric Trucks Due to Battery Fire Risk

    Volvo Trucks North America is recalling 2023-2025 VNR Electric trucks because loose hardware in the high-voltage battery may cause a short circuit and fire.

    Product
    VOLVO — VOLVO VNRE (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V181000·2025-03-24

    Peterbilt and Kenworth high voltage contactors can open cutting drive power

    PACCAR is recalling certain 2021-2025 Peterbilt 520, 579 and Kenworth T680 trucks because the high voltage contactors may open, causing a sudden loss of high voltage and drive power.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, 579, 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V182000·2025-03-24

    PACCAR Recalls Kenworth and Peterbilt Electric Trucks for Electrical Defect

    PACCAR is recalling specific Kenworth and Peterbilt electric trucks because a loose electrical connection in the cradle harness may cause a loss of drive power, increasing crash risk.

    Product
    KENWORTH — KENWORTH, PETERBILT K270, K370, 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V179000·2025-03-24

    Volvo Recalls Plug-In Hybrids Due to High-Voltage Battery Fire Risk

    Volvo is recalling specific 2020-2022 plug-in hybrid models because a high-voltage battery short circuit could cause a fire. Owners should stop charging until repairs are completed.

    Product
    VOLVO — VOLVO XC60, V60, S60, XC90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V178000·2025-03-21

    International truck calipers can contact suspension stopping the outer brake pad

    International is recalling certain 2019-2025 HV, MV and Workstar 7400 trucks because the caliper may contact a suspension spring or axle U-bolt and prevent the outer brake pad functioning.

    Product
    INTERNATIONAL — INTERNATIONAL MV, HV, WORKSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25191·2025-03-20

    Bella Pro Series and Cooks espresso machines recalled due to burn and laceration hazards

    Sensio recalls about 12,300 Bella Pro Series and Cooks Steam Espresso machines because the brew cup handle can eject forcefully, shattering the carafe. Eight of 18 ejection reports involved burn and laceration injuries.

    Product
    Bella Pro Series and Cooks Steam Espresso machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25188·2025-03-20

    Model Year 2025 Ski-Doo and Lynx Snowmobiles Recalled for Engine Mount Failure

    Bombardier Recreational Products recalls about 4,144 Model Year 2025 Ski-Doo and Lynx snowmobiles due to engine control module mounts that may break and cause stuck throttle, creating a crash hazard.

    Product
    Model Year 2025 Ski-Doo and Lynx snowmobiles equipped with a 600R E-TEC, 850 E-TEC or 850 E-TEC Turbo R engine
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25187·2025-03-20

    Aiper Seagull Pro Cordless Pool Cleaners Recalled for Fire and Burn Hazards

    About 32,660 Aiper Seagull Pro pool cleaners are recalled because the power adapter can overheat and catch fire. The firm reported 19 incidents of melting, smoking or fires, resulting in 5 property damage claims with no injuries.

    Product
    Aiper Seagull Pro ZT6001 cordless robotic pool cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25193·2025-03-20

    Segway Ninebot Max G30P and G30LP KickScooters Recalled for Fall Hazard

    The folding mechanism on about 220,000 Segway Ninebot Max G30P and G30LP KickScooters can fail during use, causing the handlebars to fold and posing a fall hazard. Segway has received 68 reports of failures, including 20 injuries.

    Product
    Segway Ninebot Max G30P and Max G30LP KickScooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0633-2025·2025-03-19

    Ulker Biskrem Cocoa Biscuits Recalled for Undeclared Wheat and Egg

    ZB Importing LLC recalls Ulker Biskrem Cocoa Biscuits due to undeclared wheat and egg. Consumers with these allergies should not consume the product.

    Product
    Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1289-2025·2025-03-19

    Portex Endotracheal Tubes may deliver inadequate ventilation due to smaller diameter

    Portex Endotracheal Tubes from Smiths Medical ASD, Inc. may have a smaller diameter than expected, potentially causing inadequate ventilation and patient hypoxia.

    Product
    Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127/035 100/141/025 100/141/030 100/141/035
    Category
    Medical Device
    Distribution
    Distributed nationwide