The Recall Desk

State

Alaska product recalls

73,381 recalls have nationwide distribution and so reach Alaska. 1,765 additional recalls listed Alaska specifically in their distribution scope.

What the numbers show

Total
1,765
Critical
118
Severe
470
Most recent
2026-09-23

Of the 1,765 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 1,765 recalls whose distribution notice names Alaska specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19176–19200 of 75146

  • HighCPSC·22781·2022-09-29

    Yamaha Viking Off-Road Side-by-Side Vehicles Recalled for Brake Hazards

    Yamaha is recalling about 330 Model Year 2022 Viking Off-Road Side-by-Side vehicles because improperly installed rear brake lines can leak brake fluid and reduce vehicle control, creating crash and injury hazards.

    Product
    Yamaha Viking Off-Road Side-by-Side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22236·2022-09-29

    HyperJuice Stackable GaN USB-C Chargers Recalled for Fire Hazard

    Hyper Products is recalling about 18,200 HyperJuice Stackable GaN USB-C Chargers (models HJ414 65W and HJ417 100W) because they can overheat and pose a fire hazard. No injuries have been reported.

    Product
    HyperJuice Stackable GaN USB-C Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V722000·2022-09-28

    2023 Western Star 49X Trucks Recalled Due to Tie Rod Defects

    Certain 2023 Western Star and Freightliner trucks are being recalled because tie rod clamps may be improperly heat-treated and crack, potentially causing loss of steering control.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4700, 4900, 49X, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1764-2022·2022-09-28

    FDA expands recall: HLS Set Advanced 7.0 sterility barrier compromise

    Maquet Medical Systems USA has expanded a recall for HLS Set Advanced 7.0, a preconnected medical device used for heart and lung support, due to a potential breach in the sterility barrier that could compromise product sterility.

    Product
    BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70105.2794. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1772-2022·2022-09-28

    Serological Test Positive Control Shows False Negative Results for Hepatitis B

    Randox Serology I Positive Control may test negative for Hepatitis B surface antigen (HBsAg) on certain analyzers despite being designed as a positive control, potentially affecting laboratory quality control procedures.

    Product
    The Randox Serology I Positive Control contains the following analytes in human based plasma: Anti HIV 1/2, Anti HTLV 1/2, Anti HCV, HBsAg, Anti HBc, and Anti Treponema pallidum IgG. The product is delivered as a liquid in a kit of 3 identical ready-to-use vials of 5 mL each.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1769-2022·2022-09-28

    Hemodialysis Water Purification Unit Recalled for Missing EMI Shielding

    Fresenius is recalling 24 units of the AquaC UNO H reverse osmosis unit because internal ethernet cables lack ferrite cores, compromising electromagnetic compatibility in hemodialysis water purification systems.

    Product
    AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse osmosis unit intended for use with hemodialysis systems. Fresenius Part Number: 24-10VA-1 Vivonic Part Number: G02000970-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1765-2022·2022-09-28

    Medical device set recalled for potential sterility barrier compromise

    Maquet Medical Systems USA is recalling the BEQ-HLS 5050 (HLS Set Advanced 5.0) due to a potential breach in the sterility barrier that may compromise product sterility.

    Product
    BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70105.2797. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V721000·2022-09-28

    Rolls-Royce Phantom Headlight Coating Defect Recall

    BMW is recalling 2023 Rolls-Royce Phantom vehicles because headlights may lack metal coating, causing low beams to fail FMVSS 108 and increasing crash risk.

    Product
    ROLLS-ROYCE — ROLLS-ROYCE PHANTOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1776-2022·2022-09-28

    FDA Recalls Grappler Suture Anchors Due to Potential Breakage Risk

    Paragon 28, Inc. is recalling Grappler Suture Anchors (REF: P44-110-3010-SK, Lot 5007499) due to risk that the anchor may break upon insertion, potentially leaving debris in patients and delaying surgery.

    Product
    Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1767-2022·2022-09-28

    Medical Device Recall: CARDIOHELP HLS Set Advanced Sterility Barrier Breach

    Maquet Medical Systems is expanding its recall of the CARDIOHELP HLS Set Advanced due to a potential breach in the sterility barrier that could compromise product sterility, affecting 6,871 US units and 18,670 worldwide.

    Product
    BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70106.9078. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1766-2022·2022-09-28

    HLS Set Advanced Sterility Breach Recall for Cardiac Support Equipment

    Maquet Medical Systems USA is recalling HLS Set Advanced 5050 units due to a potential breach in the sterility barrier. The defect may result in compromised product sterility for this cardiac and respiratory support equipment.

    Product
    BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70106.9077. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1768-2022·2022-09-28

    Absorbable Gelatin Sponge Hemostat Recalled for Endotoxin Contamination

    GELITA MEDICAL GMBH recalled 3,596 boxes of ORCA FOAM hemostats after routine testing found higher than acceptable endotoxin levels. The surgical devices were distributed across the United States.

    Product
    ORCA FOAM STANDARD CUBE 10x10x10 mm, Absorbable Gelatin Sponge Hemostat, USP, REF ORCA FOAM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1738-2022·2022-09-28

    Mountain Dew Major Melon Zero 12-pack cans have incorrect sugar-content labeling

    Mountain Dew Major Melon Zero 12-pack cans sold nationwide are labeled 'Full Sugar' on the can despite containing Zero Sugar formula. The actual product is correct; only the can label is mislabeled.

    Product
    Mountain Dew Major Melon Zero, 12 FL OZ (355mL) can, sold as 12 pack. Bottled under the authority of Pepsico, Inc. Purchase, NY 10577. UPC 0 12000 20506 4 (can) UPC 0 12000 20507 1 (12 pack carton)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1770-2022·2022-09-28

    Dialysis water-treatment unit recalled for missing ferrite cores in cables

    Fresenius is recalling 6 units of the AquaC UNO H reverse osmosis unit used with hemodialysis systems due to missing ferrite cores in internal ethernet cables affecting electromagnetic compatibility.

    Product
    AquaC UNO H [120V, 60Hz, 1700VA, US-Version- a reverse osmosis unit intended for use with hemodialysis systems. Fresenius Part Number: 24-0970-1 Vivonic Part Number: G02000966-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1774-2022·2022-09-28

    Fungitell STAT IVD Assay affected by incorrect printed reconstitution instructions

    Associates of Cape Cod is recalling Fungitell STAT IVD Assay kits due to incorrect printed information on clamshells regarding reconstitution and pretreatment volumes. Users should verify procedures against official documentation before use.

    Product
    Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Ref: FT007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1771-2022·2022-09-28

    Diversatek M-Catch Retrieval Nets: incorrect inner polybag labeling

    Diversatek Healthcare is recalling M-Catch Retrieval Nets (Part Number REF 1175-01, Lot Number 001919) due to incorrect inner polybag labeling. 245 devices were distributed nationwide between September and October 2021.

    Product
    Diversatek Health, M-Catch Retrieval Nets, Part Number REF 1175-01, Quantity 5 EA/u. Used to endoscopically retrieve severed polyps, tissue samples, food bolus, and foreign bodies in the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1541-2022·2022-09-28

    Clonidine Hydrochloride 0.3 mg Tablets Recalled for Strength Mix-up

    UNICHEM PHARMACEUTICALS is recalling Clonidine Hydrochloride Tablets labeled 0.3 mg that contain 0.2 mg tablets instead. The recall affects 18,960 bottles (Lot # GCLH22005) distributed nationwide.

    Product
    CLONIDINE HYDROCHLORIDE — CLONIDINE HYDROCHLORIDE (CLONIDINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E082000·2022-09-27

    Manchester Tank Recalls Propane Tanks Due to Valve Thread Depth Defect

    Manchester Tank & Equipment Co is recalling ManTank Propane Tanks because valve thread depth is less than spec, creating a risk of propane leaks and fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E081000·2022-09-27

    Haldex Air Disc Brake Pads Recalled for Loose Retaining Clip

    Haldex is recalling certain ModulT Gen II Air Disc Brakes because a loose retaining clip may detach, creating a road hazard and increasing crash risk.

    Product
    SERVICE BRAKES, AIR:DISC:PADS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V720000·2022-09-27

    Lightning eMotors Recalls 2022 FE4 and FT3 for Brake Warning Light Defect

    Lightning eMotors is recalling 2022 FE4 and FT3 vehicles because the instrument panel may fail to display brake and ABS warning lights, increasing crash risk.

    Product
    LIGHTNING EMOTORS — LIGHTNING EMOTORS FE4, FT3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V719000·2022-09-26

    Seagrave Recalls 2022 Emergency Vehicles Due to Tie Rod Clamp Defect

    Seagrave is recalling 2022 Marauder and Capitol emergency vehicles because improperly heat-treated tie rod clamps may fail, causing a loss of steering.

    Product
    SEAGRAVE — SEAGRAVE CAPITAL, MARAUDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V718000·2022-09-26

    2023 Volkswagen Atlas Models Recalled for Brake Line Leaks

    Volkswagen is recalling 2023 Atlas and Atlas Cross Sport models due to brake lines that may leak at threaded connections. A brake fluid leak can increase stopping distance, raising crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V717000·2022-09-26

    Doosan Recalls 2021-2022 Portable Air Compressors Due to Brake Seal Leak

    Doosan is recalling 2021-2022 Portable Air Compressors because wheel bearing seals may leak grease into drum brakes, reducing braking performance and increasing crash risk.

    Product
    DOOSAN — DOOSAN PORTABLE AIR COMPRESSOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·034-2022·2022-09-24

    Behrmann Meat and Processing Inc. Recalling Ready-to-Eat Meat Products Due to Listeria Contamination

    Behrmann Meat and Processing Inc. is recalling approximately 87,382 pounds of ready-to-eat meat products because tests detected possible Listeria monocytogenes contamination. No confirmed cases of illness have been reported since the September 24, 2022 recall announcement.

    Product
    Behrmann Meat & Processing, Inc. — Behrmann Meat and Processing Inc. Recalls Various Ready-to-Eat Meat Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·033-2022·2022-09-23

    Empanadas Valrico Recalls Beef and Chicken Empanadas Produced Without Inspection

    Empanadas Valrico Inc. is recalling approximately 6,247 pounds of frozen beef and chicken empanadas produced without federal inspection. The products were distributed in Florida.

    Product
    Empanadas Valrico Inc. Recalls Beef and Chicken Empanada Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide