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 the agency’s own highest classification or reported deaths or serious injuries, 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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4576–4600 of 39749

  • SevereNHTSA·24V263000·2024-04-11

    Keystone Recalls 2024 Trailers Due to Axle Frame Contact Risk

    Keystone RV is recalling 214 specific 2024 trailer models because the suspension equalizer may allow the axle to contact the frame, increasing crash risk.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN HAMPTON, RETREAT, ASPEN TRAIL LOFT, RESIDENCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1352-2024·2024-04-10

    Mojo Non Vented Full Face Mask warning updated for magnet hazard

    SleepNet is updating safety warnings and contraindications for its Mojo Non Vented Full Face Mask due to magnet content. All 11,874 affected units are subject to this warning update.

    Product
    Mojo Non Vented Full Face Mask with Headgear, All Sizes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1114-2024·2024-04-10

    Soy bean sprouts recalled for Listeria monocytogenes contamination

    Samsung Bean Sprout is recalling 500 bags of Sam Sung Soy Bean Sprouts with a sell-by date of December 21, 2023, distributed in Virginia, due to potential Listeria monocytogenes contamination.

    Product
    Soy Bean Sprouts in a package labeled in part: Sam Sung Soy Bean Sprouts, Net Wt. 1LB have a Sell By date of December 21, 2023.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1116-2024·2024-04-10

    Dark Chocolate Cherry Granola Recalled Due to Undeclared Almond Allergen

    Kick Ash Products is recalling Dark Chocolate Cherry Granola because it contains undeclared almond, a common allergen. Affected products may be unsafe for individuals with almond allergies.

    Product
    Kick Ash Products, Door County Love Dark Chocolate Cherry Granola, 1lb, laminated resealable bag
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1357-2024·2024-04-10

    Phantom 2 Nasal Vented Mask recalled due to magnetic device interference risk

    SleepNet is recalling the Phantom 2 Nasal Vented Mask to update contraindications and warning information related to magnets in the device. The recall affects 2,417 units distributed worldwide.

    Product
    Phantom 2 Nasal Vented Mask
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1351-2024·2024-04-10

    Mojo Full Face CPAP Mask Recall: Magnet Safety Update

    SleepNet Corporation is recalling 23,042 Mojo Full Face CPAP masks worldwide because the masks contain magnets that require updated contraindications and warning language.

    Product
    Mojo Full Face with Headgear, All Sizes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1353-2024·2024-04-10

    Mojo 2 Full Face Vented Mask Recalled: Magnet Contraindications Updated

    SleepNet Corporation is recalling 2,787 units of the Mojo 2 Full Face Vented Mask due to updates needed for contraindications and warning language regarding magnets in the device. Worldwide distribution.

    Product
    Mojo 2 Full Face Vented Mask, All Sizes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1354-2024·2024-04-10

    Mojo 2 Full Face Non Vented Mask Recalled for Magnet Safety Concerns

    SleepNet Corporation is recalling Mojo 2 Full Face Non Vented Masks due to magnets in the device and updated contraindications and warnings. The recall affects 2,107 units distributed worldwide.

    Product
    Mojo 2 Full Face Non Vented Mask, All Sizes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1355-2024·2024-04-10

    Mojo 2 CPAP Masks Recalled Worldwide for Magnet Safety Contraindication Update

    SleepNet Corporation is recalling Mojo 2 Full Face CPAP masks (1,268 units worldwide) to update contraindications and warning language due to magnets in the masks. The FDA classified this as a Class I recall.

    Product
    Mojo 2 Full Face AAV Non Vented Mask, All Sizes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V258000·2024-04-10

    Hi-Tech E.V.S. Recalls 2020-2023 Spartan Fire Trucks for Wiring Defect

    Hi-Tech E.V.S. is recalling 2020-2023 Spartan Gladiator and Metrostar fire trucks because a firmware defect in specific nodes may cause electrical circuits to overheat and increase the risk of fire.

    Product
    HI-TECH E.V.S. — HI-TECH E.V.S. SPARTAN GLADIATOR, SPARTAN METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1356-2024·2024-04-10

    iQ 2 Nasal Vented Mask Recalled for Magnet Safety Warnings

    SleepNet Corporation is recalling the iQ 2 Nasal Vented Mask due to magnets requiring updated contraindication and warning language. Approximately 2,477 units distributed worldwide are affected.

    Product
    iQ 2 Nasal Vented Mask
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V253000·2024-04-05

    Forest River Recalls Transit Buses Due to Unsecured Brake Lines

    Forest River Bus is recalling specific 2018-2024 transit bus models because unsecured brake lines may be damaged by the frame rail, increasing crash risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, ELDORADO, ELKHART SENATOR II, CANDIDATE II, ADVANTAGE, ALLSTAR MVP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V080000·2024-04-05

    Autocar Recalls 2023 Xpeditor and Xspotter Vehicles for Steering Defect

    Autocar is recalling 2023 Xpeditor and Xspotter vehicles because steering gears may have fewer recirculating balls than required, risking loss of steering control.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24180·2024-04-04

    C2 Crank Cocking Aids for Excalibur Crossbows Recalled for Impact Injury and Laceration Hazards

    Excalibur Crossbow is recalling about 15,000 C2 Crank cocking aids because the plastic cocking hooks can break during use and become flying projectiles, causing impact injuries and lacerations. One consumer reportedly suffered a permanent eye injury.

    Product
    C2 Crank Cocking Aid for Crossbows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·24179·2024-04-04

    Essential Medical Supply Reannounces Adult Bed Rails Recall; Entrapment and Asphyxia

    Essential Medical Supply is reannouncing a recall of approximately 272,000 Endurance® Hand Bed Rails due to entrapment and asphyxiation hazards. Two additional deaths have been reported since the original 2021 recall.

    Product
    Endurance® Hand Bed Rails
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·24181·2024-04-04

    BLACK+DECKER Garment Steamers Recalled Nationwide for Burn Hazard

    Empower Brands is recalling approximately 1.6 million BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, causing burn injuries. Consumers should stop using the steamers immediately and contact the manufacturer for a full refund.

    Product
    BLACK+DECKER Model HGS011 Easy Garment Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V252000·2024-04-04

    Terex Advance Recalls 2023 Commander Vehicles for Steering Defect

    Terex Advance is recalling 2023 Commander vehicles because steering components may not be installed correctly, increasing the risk of a crash.

    Product
    TEREX ADVANCE — TEREX ADVANCE COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1302-2024·2024-04-03

    Boston Scientific steerable sheath devices recalled due to manufacturing defect risk

    Boston Scientific is recalling 461 POLARSHEATH Steerable Sheath devices due to a manufacturing tooling error that may cause inner sheath delamination and potential fragment release during medical procedures.

    Product
    Boston Scientific POLARSHEATH Steerable Sheath 12F, REF M004CRBS3050
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1326-2024·2024-04-03

    Catheter Extension Recalled by Fresenius Due to Chemical Leachables

    Fresenius is recalling 479,978 stay-safe Luer Lock Catheter Extensions due to chemical leachables in the tubing. Healthcare providers should contact the manufacturer for replacement information.

    Product
    stay-safe /Luer Lock Catheter Ext. 18 in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1107-2024·2024-04-03

    Trader Joe's Roasted and Salted Cashews Recalled Due to Salmonella Risk

    Trader Joe's 50% Less Sodium Roasted & Salted Whole Cashews are being recalled due to potential Salmonella contamination. The recall affects 6,001 cases distributed in California, Washington, and Texas.

    Product
    Trader Joe's 50% Less Sodium Roasted & Salted Whole Cashews Net Wt. 15 oz (1 LB) 454g Dist. & Sold Exclusively By: Trader Joe's, Monrovia, CA 91016 Cashews Product of India and Vietnam
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1286-2024·2024-04-03

    Nimbus II Infusion Pump Systems Recalled for Multiple Potential Device Failures

    InfuTronix is recalling 52,328 Nimbus II Infusion Pump Systems due to potential failure modes including battery failure, system errors, drug product leakage, flow rate issues, and housing damage. The devices will no longer be available or supported after June 20, 2024.

    Product
    Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078; Nimbus II EpiD IT1124; Nimbus II EMS IT1063; Ambulatory Infusion Pump and components
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1323-2024·2024-04-03

    Catheter Extension Tubing Recalled Due to Identified Leachable Substances

    Fresenius Medical Care is recalling 114,982 stay-safe Safe Lock Catheter Extensions due to peroxide cross-linked tubing leachables. Patients and healthcare providers are advised to discontinue use and contact the manufacturer for replacement.

    Product
    stay-safe /Safe Lock Catheter Ext. 12 in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V248000·2024-04-03

    Aston Martin Recalls 2021 DBX Vehicles for Loose Driveline Fasteners

    Aston Martin is recalling 2021 DBX vehicles because loose fasteners on the front propeller shaft and differential may cause loss of front wheel drive or engine stall.

    Product
    ASTON MARTIN — ASTON MARTIN DBX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1099-2024·2024-04-03

    Great Value Honey Roasted Cashews Recalled for Undeclared Milk and Coconut Allergens

    Great Value Honey Roasted Cashews (8.25 oz cans, UPC 0 78742 13334 8) are being recalled due to undeclared milk and coconut allergens on the packaging. Consumers with allergies to these ingredients should not consume the product.

    Product
    Great Value Honey Roasted Cashews, 8.25oz. plastic can, UPC 0 78742 13334 8
    Category
    Food
    Distribution
    30 states