The Recall Desk

State

Alaska product recalls

72,940 recalls have nationwide distribution and so reach Alaska. 1,764 additional recalls listed Alaska specifically in their distribution scope.

What the numbers show

Total
1,764
Critical
118
Severe
350
Most recent
2026-09-09

Of the 1,764 recalls naming Alaska we have scored against our rubric, 118 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 350 (20%) are Severe.

These figures cover only the 1,764 recalls whose distribution notice names Alaska specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3676–3700 of 74704

  • ModerateFDA (Devices)·Z-1062-2026·2026-01-21

    Allura Xper FD10C systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 38 Allura Xper FD10C systems because the drip tray beneath the cooling unit may not have been installed.

    Product
    Product Name: Allura Xper FD10C; Model number: 722001;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1054-2026·2026-01-21

    Facial procedure packs recalled over recalled B. Braun administration sets inside

    Medline is recalling 16 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
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: DR HOLCOMB FACIAL PACK, Medline kit SKU DYNJ54488A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1068-2026·2026-01-21

    Allura Xper FD10, model 722026, recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 95 units of the Allura Xper FD10, model 722026, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD10; Model Number: 722010;
    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
  • 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-0274-2026·2026-01-21

    Admission and admin kits recalled over recalled B. Braun administration sets

    Medline is recalling 1725 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
    CHILDREN NYQUIL, COLD&FLU, BERRY, 8oz, 12ct
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (Devices)·Z-1051-2026·2026-01-21

    Pre-op kits recalled because they contain recalled B. Braun administration sets

    Medline is recalling 32 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
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.
    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-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-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
  • 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 425 COMMERCIAL SHELL, COMMERCIAL VEHICLE, VIEW, 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 G80 ELECTRIFIED, G80, GV60, GV80
    Category
    Vehicle
    Distribution
    Distributed nationwide