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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851–875 of 36490

  • SevereCPSC·26435·2026-04-23

    32 Degrees heated socks have caused first- and second-degree burns

    32 Degrees heated socks sold at Costco are recalled after 14 heat-related incidents, 13 of them involving first- or second-degree burns. About 207,806 units are affected.

    Product
    32 Degrees Heated Socks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26431·2026-04-23

    FitRx adjustable dumbbell weight plates can dislodge from the handle

    FitRx SmartBell Quick-Select adjustable dumbbells are recalled after more than 115 reports of weight plates dislodging during use, with at least six injuries including broken toes.

    Product
    FitRx SmartBell Quick-Select 5-52.5lbs Adjustable Dumbbells
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V264000·2026-04-23

    REV Recalls 2026 Motorhomes Due to Unexpected Generator Activation

    REV is recalling 2026 Fleetwood and Holiday Rambler motorhomes because a furnace defect may turn on the generator unexpectedly, posing a carbon monoxide risk.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FORTIS, VACATIONER, ADMIRAL, FLAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1799-2026·2026-04-22

    B. Braun Hemodialysis Bloodlines Recalled Due to Potential Air Bubble Accumulation

    B. Braun Medical Inc is recalling STREAMLINE BLOODLINE SET FOR DIALOG (Model Number: SL-2010M2096) because air bubbles may accumulate in the arterial line.

    Product
    B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Number: SL-2010M2096
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1798-2026·2026-04-22

    B. Braun StreamLine Dialog DR bloodlines may accumulate arterial air bubbles

    B. Braun is recalling StreamLine Bloodline Sets for Dialog DR because small air bubbles can accumulate in the arterial line under negative pressure. 3,158,104 units are affected.

    Product
    B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR. Model Number: SL-2010M2096A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1802-2026·2026-04-22

    B. Braun hemodialysis bloodlines may accumulate air bubbles in the arterial line

    B. Braun is recalling one model of hemodialysis bloodline because small air bubbles can accumulate in the arterial line when blood gases adhere to the tubing under negative pressure.

    Product
    B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model Number: B3-3632M3705.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V256000·2026-04-22

    Toyota RAV4 front seat brackets may be welded improperly

    Toyota is recalling certain 2025 RAV4 vehicles because the front seat brackets for the seat rails may be welded improperly, which can prevent the seat from restraining an occupant in a crash.

    Product
    TOYOTA — TOYOTA RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V258000·2026-04-22

    Volkswagen Taos fuel pressure sensor may separate in a rear-end crash

    Volkswagen is recalling certain 2025-2026 Taos vehicles because the fuel pressure sensor may dislodge from the fuel tank in a rear-end crash, failing FMVSS 301 fuel system integrity.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1803-2026·2026-04-22

    B. Braun 4.8 mm hemodialysis bloodlines may accumulate arterial air bubbles

    B. Braun is recalling hemodialysis bloodlines with a 4.8 mm pump segment because small air bubbles can accumulate in the arterial line under negative pressure. 4,884 units are affected.

    Product
    B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1797-2026·2026-04-22

    Omnipod 5 insulin pods from 49 lots have torn internal cannulas

    Omnipod 5 Pods from 49 lots have an internal soft cannula tear that lets insulin leak inside the Pod instead of being delivered. 1,240,115 units are affected.

    Product
    Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1801-2026·2026-04-22

    B. Braun StreamLine long bloodlines may accumulate arterial air bubbles

    B. Braun is recalling StreamLine Bloodline Long Version sets because small air bubbles can accumulate in the arterial line under negative pressure. 328,640 units are affected.

    Product
    B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1800-2026·2026-04-22

    B. Braun StreamLine Fresenius bloodlines may accumulate arterial air bubbles

    B. Braun is recalling StreamLine Fresenius bloodlines supplied for DaVita because small air bubbles can accumulate in the arterial line under negative pressure. 1,174,271 units are affected.

    Product
    B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V255000·2026-04-21

    Tesla Cybertruck brake rotor stud holes may crack and separate

    Tesla is recalling certain 2024-2026 Cybertruck vehicles with 18-inch steel wheels because brake rotor stud holes may crack and allow the stud to separate from the wheel hub.

    Product
    TESLA — TESLA CYBERTRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V252000·2026-04-20

    Mitsubishi Outlander liftgate gas springs may corrode and lose pressure

    Mitsubishi is recalling certain Outlander and Outlander PHEV vehicles because the liftgate gas spring cylinders may corrode and lose pressure, risking rupture or a falling liftgate.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26T011000·2026-04-18

    Goodyear Eagle F1 Supersport Tires Recalled for Tread Separation Risk

    Goodyear is recalling specific Eagle F1 Supersport tires because the tread may separate, increasing the risk of a crash. Owners should contact Goodyear for a free replacement or refund.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V247000·2026-04-17

    Altec Recalls 2025-2026 Digger Derrick and Aerial Devices for Radar Defect

    Altec is recalling 2025-2026 Digger Derrick and Aerial Device vehicles because improperly installed front-end radar may cause unexpected brake activation, increasing crash risk.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V248000·2026-04-17

    Land Rover and Jaguar mild hybrids may lose drive power from converter fault

    Jaguar Land Rover is recalling certain mild-hybrid vehicles because the DC-DC converter can fail due to an internal fault, causing a loss of drive power. 170,169 vehicles are affected.

    Product
    LAND ROVER — LAND ROVER, JAGUAR DEFENDER, RANGE ROVER EVOQUE, RANGE ROVER, DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E021000·2026-04-16

    Chrysler Recalls Mopar Engines Due to Debris-Related Fire Risk

    Chrysler is recalling specific Mopar engines where internal debris may cause failure, leading to loss of drive power or engine compartment fire.

    Product
    ENGINE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26414·2026-04-16

    SEGMART toddler trampoline accessory straps pose a strangulation hazard to children

    SEGMART toddler trampoline accessory kits are recalled because children can become entangled in the hammock, punching bag and hand ring straps. One child suffered a rope burn to the neck.

    Product
    SEGMART 55" Indoor/Outdoor Mini Round Toddler Trampolines with Enclosure Nets and Accessory Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26409·2026-04-16

    Magic Pocket Staffs can expand unintentionally, causing eye and face injuries

    nvyue Magic Pocket Staffs are recalled after 163 reports of injuries to the eyes, face and hands, including corneal lacerations and temporary vision loss. About 25,000 units are affected.

    Product
    nvyue Magic Pocket Staffs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0653-2026·2026-04-15

    Boner Bears Honey Male Enhancement contains undeclared pharmaceutical drugs

    Pure Vitamins and Natural Supplements, LLC is recalling Boner Bears Honey Male Enhancement because FDA testing found undeclared sildenafil and tadalafil, prescription drugs not listed on the label.

    Product
    Boner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume 1 entire pouch 30 minutes before Intercourse. MANUFACTURED IN: FLORIDA. UPC 788362191603
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1727-2026·2026-04-15

    Medline delivery packs recalled over syringe rotating adaptor disconnection risk

    Medline is recalling Delivery Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. DELIVERY PACK, Medline SKU # DYNJ42892F; 2. DELIVERY PACK, Medline SKU # DYNJ42892G.
    Category
    Medical Device
    Distribution
    Distributed nationwide