The Recall Desk

State

Alaska product recalls

73,503 recalls have nationwide distribution and so reach Alaska. 1,766 additional recalls listed Alaska specifically in their distribution scope.

What the numbers show

Total
1,766
Critical
118
Severe
470
Most recent
2026-10-14

Of the 1,766 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 470 (27%) are Severe.

These figures cover only the 1,766 recalls whose distribution notice names Alaska specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23626–23650 of 75269

  • SevereNHTSA·21V805000·2021-10-15

    Ford vehicles recalled for damaged side impact airbag sensors

    Ford is recalling certain 2022 and 2021 model vehicles due to damaged side impact airbag sensors that may fail to deploy properly in a crash.

    Product
    FORD — FORD, LINCOLN F-150, F-350 SD, F-250 SD, EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V806000·2021-10-15

    Yamaha Recalls 2020-2021 XVS950 Motorcycles Due to Engine Oil Leak

    Yamaha is recalling 2020-2021 XVS950 motorcycles because the engine case may leak oil onto the rear tire, increasing the risk of a crash.

    Product
    YAMAHA — YAMAHA BOLT R-SPEC XVS950
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V812000·2021-10-15

    2021 Volkswagen Atlas front wheel bearing bolts may loosen and cause crash risk

    Volkswagen is recalling certain 2021 Atlas, Atlas Cross Sport, and Passat vehicles because the front wheel bearing bolts may have been incorrectly tightened and could loosen, potentially causing loss of control and crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, PASSAT, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V809000·2021-10-15

    2021 Ford Bronco Sport Moonroof Glass May Detach from Vehicle

    Ford is recalling certain 2021 Bronco Sport vehicles because the moonroof glass may not be bonded correctly to the frame and could detach. A detached glass panel could become a road hazard and increase crash risk.

    Product
    FORD — FORD BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V814000·2021-10-15

    2022 KZRV Sporttrek and Stratus Trailers Fire Risk Recall

    KZRV is recalling certain 2022 Sporttrek and Stratus trailers due to improper circuit breaker connections in water heater and fireplace circuits. The incorrect amperage could increase fire risk.

    Product
    KZRV — KZRV STRATUS, SPORTTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V810000·2021-10-15

    Smeal Recalls 2021 Pumper Fire Trucks Due to Lifting Cable Defect

    Smeal Holding, LLC is recalling one 2021 Pumper Fire Apparatus because improperly crimped lifting cables may cause the generator set to fall, increasing injury risk.

    Product
    SMEAL — SMEAL PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V798000·2021-10-14

    RAM Pickup and Cab Chassis Trucks: Intake Heater Relay Fire Risk

    Certain 2021-2022 RAM pickup and cab chassis trucks with Cummins diesel engines may experience electrical shorts in the Intake Heater Grid Relay, causing a fire hazard. Owners should park outside until dealers inspect and repair the defect.

    Product
    RAM — RAM 2500, 4500, 3500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V800000·2021-10-14

    Volvo Recalls 2001-2007 V70 and XC70 for Air Bag Inflator Defect

    Volvo is recalling 2001-2007 V70 and XC70 vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    VOLVO — VOLVO V70, XC70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V799000·2021-10-14

    Van Hool Buses Recalled for Wheelchair Lift Barrier Defect

    Van Hool is recalling 422 buses because wheelchair lift barriers may fail under force, increasing injury risk.

    Product
    VAN HOOL — VAN HOOL T2145, C2045, CX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V797000·2021-10-14

    2021 Jeep Grand Cherokee High Beam Headlights May Not Activate

    In certain 2021 Jeep Grand Cherokee L vehicles, the high beam headlights will not activate when the lighting switch is in auto position unless the switch is first changed to on. This defect reduces visibility and increases crash risk.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0004-2022·2021-10-13

    Betaxolol Ophthalmic Solution Recalled for Sterility Failure

    Akorn, Inc. is recalling Betaxolol Ophthalmic Solution, USP 0.5% due to confirmed sterility failure detected during stability testing. The affected lot was distributed nationwide.

    Product
    Betaxolol Ophthalmic Solution, USP, 0.5%, (Betaxolol HCl 5.6 mg/mL), 5 mL dropper bottle, Rx only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Carton NDC: 17478-705-10, Bottle NDC 17478-705-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0001-2022·2021-10-13

    ALPHA MALE+ Male Enhancer Fruit Chew Strips Recalled for Unapproved Drug

    ALPHA MALE+ Male Enhancer fruit chew strips are being recalled because they contain tadalafil and were marketed without FDA approval. Consumers should stop using the product and consult a healthcare provider if they have questions.

    Product
    ALPHA MALE+ Male Enhancer, fruit chew strips, 1 strip per foil pouch, Distributed by Umbrella Labs, Made in the USA, UPC 8 60003 03770 6. Also manufactured for and distributed by: Alpha Male Plus, Tucson, AZ UPC 8 60003 74518 2 (pouch), UPC 8 60003 74512 0(carton)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·038-2021·2021-10-13

    Butterball Recalls Ground Turkey Products Due to Possible Blue Plastic Contamination

    Butterball is recalling approximately 14,107 pounds of ground turkey products that may contain blue plastic. The recall covers specific 2.5-lb and 3-lb trays sold nationwide.

    Product
    Butterball, LLC — Butterball, LLC Recalls Ground Turkey Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0010-2022·2021-10-13

    FDA Recalls Ultrasound Gels and Lotions for Potential Bacterial Contamination

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical may contain bacterial contamination. The FDA has issued a Class I recall affecting 8,702 units distributed worldwide.

    Product
    Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon bottle, REF: 4210, located in the following DJO, LLC / DJO FRANCE kits:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V795000·2021-10-13

    Zero SR/F Motorcycles Recalled for Loose Rear Rotor Bolts

    Zero Motorcycles is recalling 2020 SR/F motorcycles because insufficiently tightened rear rotor bolts may reduce braking capability and increase crash risk.

    Product
    ZERO — ZERO SR/F
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0002-2022·2021-10-13

    Artesunate for Injection Recalled Due to Sterility Assurance Failure

    AMIVAS (US), LLC is recalling Artesunate for Injection (110 mg/vial) because an air filter failed post-integrity testing, creating a lack of sterility assurance for the product.

    Product
    Artesunate for Injection, 110 mg/vial, packaged in a) 2x2 pack containing 2 Single-dose vials artesunate (73607-001-01) and 2 vials sterile diluent (NDC 73607-001-02) per carton (NDC 73607-001-11); 4x4 pack containing 4 Single-dose vials artesunate (73607-001-01) and 4 vials…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0003-2022·2021-10-13

    Firvanq Vancomycin Oral Solution Kits Recalled for Incorrect Diluent

    Azurity Pharmaceuticals is recalling 2,751 kits of Firvanq (vancomycin hydrochloride for oral solution) distributed nationwide because an incorrect diluent component was included in the kit.

    Product
    FIRVANQ — FIRVANQ (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0009-2022·2021-10-13

    Ultrasound gel distributed with medical devices recalled for bacterial contamination

    Ultrasound gel manufactured by Eco-Med Pharmaceutical and distributed with various medical device kits may contain bacterial contamination. Users should stop using affected products and follow FDA guidance.

    Product
    GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO FRANCE in the following kits, Part/Description: 2073/ INTELECT RPW 120V, 2073-BR/ INTELECT RPW 120V BRAZIL, 2074/ INTELECT RPW 230 V…
    Category
    Medical Device
    Distribution
    Distributed nationwide