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.

Filters

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

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

4626–4650 of 113838

  • ModerateFDA (Devices)·Z-1083-2026·2026-01-21

    Procedure kits recalled over suction irrigators that can leak during use

    Medline is recalling 4,536 procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.

    Product
    Brand Name: PALACOS Product Name: PALACOS MV pro 40; PALACOS MV pro 80 Model/Catalog Number: 5150633; 5150635 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1061-2026·2026-01-21

    Hydrophilic catheters recalled over an incorrect expiration date on labeling

    Hangzhou Bever Medical Devices is recalling 149,310 BD Ready-to-Use Hydrophilic Catheters, 14 Fr, over a labeling error giving an incorrect expiration date.

    Product
    BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0402-2026·2026-01-21

    Mandible and ear procedure packs recalled over recalled B. Braun sets

    Medline is recalling 96 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Atwater's, Holiday Cookie Tin, 19.65 ounces, Round metal tin with a window lid
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0256-2026·2026-01-21

    Fluocinolone topical solution recalled after failing an impurity specification

    Sun Pharmaceutical Industries is recalling 24,624 bottles of Fluocinolone Acetonide Topical Solution 0.01% after an out of specification result for a known impurity.

    Product
    FLUOCINOLONE ACETONIDE — FLUOCINOLONE ACETONIDE (FLUOCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0259-2026·2026-01-21

    Carotid anesthesia kits recalled over recalled B. Braun administration sets inside

    Medline is recalling 10 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0280-2026·2026-01-21

    PALACOS MV plus G bone cement recalled because ampoules may not break

    Heraeus Medical is recalling PALACOS MV+G pro 40 and PALACOS MV+G pro 80 bone cement because an unfortunate combination of factors can leave ampoules unbroken, so no appropriate cement dough is formed.

    Product
    Swan, White Clear Alcohol, 50%, 16oz, 12 count
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1073-2026·2026-01-21

    Allura Xper FD20 Biplane, model 722013, recalled over a missing drip tray

    Philips Medical Systems Nederland is recalling 23 units of the Allura Xper FD20 Biplane, model 722013, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD10; Model Number: 722026;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1040-2026·2026-01-21

    CT pendant replacement kits recalled for missing a safe hand position label

    Mobius Imaging is recalling 101 detachable 10in pendant replacement components for the AIRO CT X-ray System because they do not carry the Safe Hand Position Warning label.

    Product
    Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1048-2026·2026-01-21

    Infusion system software recalled to emphasize instructions in the manual

    Fresenius Kabi is recalling 30 units of Ivenix Infusion System LVP software to emphasize the instructions for LVP duration programming set out in the IFU.

    Product
    Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1041-2026·2026-01-21

    CT pendant upgrades recalled for missing a safe hand position label

    Mobius Imaging is recalling 26 detachable 10in pendant upgrade components for the AIRO CT X-ray System because they do not carry the Safe Hand Position Warning label.

    Product
    Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography (CT) X-ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V023000·2026-01-20

    2025 Nissan Sentra door strikers may fail while vehicle in motion

    Nissan is recalling certain 2025 Sentra vehicles because door strikers may have been improperly welded and could break, allowing doors to open while the vehicle is moving. This increases the risk of injury or crash.

    Product
    NISSAN — NISSAN SENTRA, ALTIMA, KICKS, FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26C001000·2026-01-20

    Evenflo Recalls Titan 65 Child Seats Missing Tether Straps

    Evenflo is recalling specific Titan 65 child seats that may lack a tether strap, which could reduce crash protection and increase injury risk.

    Product
    CHILD SEAT:TETHER: STRAP/WEBBING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V020000·2026-01-19

    Fifth wheel trailer ramp door may break away from its frame

    Forest River is recalling certain fifth wheel travel trailers across the Work and Play, Coachmen Adrenaline, Chaparral, Riverstone, Takoda, Shasta Phoenix and Cedar Creek ranges because the ramp door may break away.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN, SHASTA CEDAR CREEK, CHAPARRAL, RIVERSTONE, ADRENALINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·001-2026·2026-01-16

    Suzanna's Kitchen Recalls Grilled Chicken Breast Fillets Due to Listeria Risk

    Suzanna's Kitchen is recalling approximately 13,720 pounds of ready-to-eat grilled chicken breast fillets due to possible Listeria monocytogenes contamination.

    Product
    Suzanna's Kitchen Inc — Suzanna’s Kitchen Recalls Ready-To-Eat Grilled Chicken Breast Fillet Products due to Possible Listeria Contamination
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·26V015000·2026-01-16

    Newmar Recalls 2026 Freedom Aire Motorhomes Due to Fire Risk

    Newmar is recalling 2026 Freedom Aire motorhomes because a water tank heating pad may fail, increasing the risk of a fire.

    Product
    NEWMAR — NEWMAR FREEDOM AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V016000·2026-01-16

    Winnebago water tank heating pad may fail from high resistance

    Winnebago is recalling certain motorhomes equipped with a ThermaHeat Tank Pad because the water tank heating pad may experience high resistance and fail, increasing the risk of a fire.

    Product
    WINNEBAGO — WINNEBAGO MINNIE WINNIE, TRAVATO, SPIRIT, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V017000·2026-01-16

    Lucid Air rearview camera image may not display when reversing

    Lucid is recalling certain 2022-2026 Air vehicles with the AD02 package on software versions 2.8.0 through 2.8.16, because the rearview camera image may not display when the vehicle is in reverse.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V019000·2026-01-16

    2025–2026 Genesis GV80, G80, GV70, GV60 instrument panel display software error

    Hyundai is recalling certain 2025–2026 Genesis vehicles because a software error may cause the instrument panel display to fail, potentially hiding critical safety information like the speedometer and fuel gauge.

    Product
    GENESIS — GENESIS GV60, G80, G80 ELECTRIFIED, GV80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26E004000·2026-01-16

    Lippert Recalls Bus Windows with Illegible DOT Markings

    Lippert is recalling certain bus windows that may have illegible DOT markings, failing to comply with Federal Motor Vehicle Safety Standard 205.

    Product
    VISIBILITY:GLASS, SIDE/REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide