The Recall Desk

State

Alaska product recalls

73,495 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 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23026–23050 of 75261

  • SevereNHTSA·21V981000·2021-12-16

    Terex Advance Mixer Trucks Recalled for Fuel Leak Fire Risk

    Terex is recalling 2016-2022 Front Discharge Mixer trucks because fuel tubes may crack, causing high-pressure leaks that increase fire risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E101000·2021-12-16

    Bosch High Pressure Fuel Pump Recall for Engine Stall Risk

    Robert Bosch is recalling high pressure fuel pumps for BMW and Chrysler vehicles due to a risk of sudden engine stall while driving.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V986000·2021-12-16

    Ford Recalls 2021-2022 F-150 Trucks for Driveshaft Fracture Risk

    Ford is recalling 2021-2022 F-150 vehicles because underbody insulators may loosen and damage the driveshaft, potentially causing loss of vehicle control.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22712·2021-12-16

    Northern Lights Alaura Two-Tone Jar Candles Recall Due to Laceration and Fire Hazards

    Northern Lights is recalling Alaura Two-Tone Jar Candles sold at Costco because the glass containers can shatter, crack, or break while burning, posing laceration and fire hazards. The company has received 138 reports of breakage, including three reports of laceration injuries.

    Product
    Alaura Two-Tone Jar Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V979000·2021-12-16

    2021-2022 Ford Mustang Mach-E and 2022 Maverick seat belt attachment recall

    Ford is recalling 2021-2022 Mustang Mach-E and 2022 Maverick vehicles due to improperly attached rear seat belt buckles. The defect may prevent proper occupant restraint in a crash, creating an injury risk.

    Product
    FORD — FORD MUSTANG MACH E, MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V982000·2021-12-16

    2021 Ford Bronco Radar Misalignment Affects Cruise Control and Emergency Braking

    Ford is recalling certain 2021 Bronco and Ranger vehicles due to a misaligned cruise control radar module that may prevent the adaptive cruise control and emergency braking systems from functioning properly, increasing crash risk.

    Product
    FORD — FORD RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V983000·2021-12-16

    Ford Recalls 2018 F-150 Trucks for Tailgate Latch Defect

    Ford is recalling 2018 F-150 trucks because tailgate latches may open unexpectedly while driving, creating a road hazard.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V987000·2021-12-16

    2021 Honda Rebel 1100 Radiator Cap May Leak Hot Coolant

    Honda is recalling 2021 Rebel 1100 motorcycles because the radiator cap may have been improperly formed, creating an insufficient seal. A leaking cap could spray hot coolant, increasing risk of injury or crash.

    Product
    HONDA — HONDA REBEL 1100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V980000·2021-12-16

    2021 Ford Mustang side curtain air bags may not inflate properly

    Ford is recalling 2021 Mustang vehicles because the side curtain air bag inflators may have been manufactured with incorrect gas pressure, potentially resulting in improper inflation during a crash.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22713·2021-12-16

    Karmas Far Infant Bath Seats Recalled for Drowning Hazard

    Karmas Far infant bath seats fail federal safety standards and can tip over during use, posing a drowning hazard to babies. About 900 units sold online between August 2017 and October 2021 are affected. No injuries have been reported.

    Product
    Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V985000·2021-12-16

    Chevrolet and GMC Trucks: Spare Tire Incompatibility Disables Braking System

    General Motors is recalling certain 2019-2021 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks. The supplied 17-inch spare tire is incompatible with aftermarket wheels, disabling the anti-lock braking system and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0344-2022·2021-12-15

    Puritan Bennett 980 Series Ventilators Recalled for Incorrect Capacitor Assembly

    Covidien is recalling 278 Puritan Bennett 980 Series Ventilators worldwide due to incorrect capacitor assembly that may cause devices to become inoperable during patient use.

    Product
    Puritan Bennett 980 Series Ventilator, 980U3ESDIUU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V971000·2021-12-15

    MCI Recalls Diesel Buses Due to Fuel Tube Fire Risk

    Motor Coach Industries is recalling 1,125 diesel buses because fuel tubes may crack and leak, increasing the risk of fire.

    Product
    MCI — MCI D45CRTLE, D4520, D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0342-2022·2021-12-15

    Puritan Bennett 980 Ventilator Recalled for Capacitor Assembly Error

    Puritan Bennett 980 Series Ventilators are recalled due to an assembly error in a capacitor that may cause the device to become inoperable during use. The recall affects 278 units.

    Product
    Puritan Bennett 980 Series Ventilator, 980U1ENASAA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0339-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recalled for Assembly Defect

    Covidien is recalling Puritan Bennett 980 Series Ventilators due to an assembly error in a capacitor. The defect may cause the ventilator to become inoperable during use.

    Product
    Puritan Bennett 980 Series Ventilator, 980A3ENNISB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0266-2022·2021-12-15

    AmericanScreening Hand Sanitizer Recalled for Misleading Bottle Resemblance

    AmericanScreening Hand Sanitizer (ethyl alcohol 70%), 8 FL OZ bottles, is being recalled nationwide because the containers resemble drinking water bottles, posing a risk of accidental ingestion.

    Product
    AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA Vitamin E & Moisturizer, 8 FL OZ (237 mL) bottle with either a black or clear top, Distributed by American Screening LLC Shreveport, LA, 71106 UPC 8 40050 51579 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0343-2022·2021-12-15

    Puritan Bennett 980 Ventilator Recalled for Capacitor Assembly Error

    Covidien is recalling the Puritan Bennett 980 Series Ventilator due to incorrect capacitor assembly that may cause the device to become inoperable during patient use.

    Product
    Puritan Bennett 980 Series Ventilator, 980U1ESDIUC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0341-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recall Due to Manufacturing Defect

    Covidien is recalling 278 Puritan Bennett 980 Series Ventilators due to a manufacturing error where a capacitor was assembled incorrectly, which may cause the device to become inoperable during use.

    Product
    Puritan Bennett 980 Series Ventilator, 980S3ENDICU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0245-2022·2021-12-15

    North Coast Smoked Salmon Trim Recalled for Listeria Contamination

    Oregon Lox Company is recalling North Coast Smoked Salmon Trim (3 lb packages, UPC 008603002551) due to potential Listeria monocytogenes contamination. The product was distributed in Alaska, California, Oregon, and Washington.

    Product
    North Coast Smoked Salmon Trim - Partial Slices of Cold Smoked Salmon, net wt. 3 lb. UPC 008603002551. The Ingredients statement on the label are read in parts: "***INGREDIENTS: Salmon, salt, brown sugar, sodium nitrite, FD&C Yellow 6/Red 40, natural hardwood smoke…
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0346-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recalled for Capacitor Assembly Defect

    Covidien is recalling 278 Puritan Bennett 980 Series Ventilators (Model 980X1ENDIPC) due to incorrect capacitor assembly that may cause the device to malfunction during use.

    Product
    Puritan Bennett 980 Series Ventilator, 980X1ENDIPC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0335-2022·2021-12-15

    OsteoMed Surgical Consoles Recalled for Electrical Safety Violations

    OsteoMed OsteoPower Power Consoles and footswitches are being recalled due to non-compliance with electrical safety standard IEC 60601. The product has shocked a patient, creating a significant electrical hazard.

    Product
    OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control Console 2 REF 450-0021-01 -Power Control Console 2 REF ECOS-450-0021-00 -OsteoMed OsteoPower Power Console 2i REF 450-0005-00 -OsteoMed D-Power Control…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0349-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator recalled for assembly defect

    Puritan Bennett 980 Series Ventilators are recalled due to a capacitor assembly error that may cause the device to become inoperable during use. The recall affects 278 units distributed worldwide.

    Product
    Puritan Bennett 980 Series Ventilator, 980X1JADIJJ
    Category
    Medical Device
    Distribution
    Distributed nationwide