Alaska recalls

1,901 federal recalls affecting Alaska in the last 12 months: 27 sold in Alaska plus 1,874 sold nationwide. From the CPSC, FDA, USDA and NHTSA.

Recent recalls

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  • Currey & Company Nottaway chandeliers recalled for electrocution risk

    Sold nationwide. Currey & Company's Nottaway chandeliers lack proper electrical grounding, which can cause electrocution. The affected two-tier and three-tier models were sold in gold, bronze, and champagne finishes between November 2025 and May 2026. Only chandeliers with no visible screw on the outside of the top distributor cap are affected.

    SeriousCPSCJul 16, 2026Currey &

  • Boon PIVOT toddler towers recalled for tip-over risk

    Sold nationwide. The Boon PIVOT toddler tower kitchen step stool can tip over or shift during use, creating a risk of serious injury. TOMY has received 11 reports of the stools becoming unstable or leaning, though no injuries have been reported yet.

    SeriousCPSCJul 16, 2026Tomy

  • Liizousuda paint thinner recalled for child poisoning risk

    Sold nationwide. Liizousuda paint thinner bottles sold on Amazon have regular caps that children can open easily. The product contains petroleum distillates that can cause serious injury or death if swallowed, and can damage the lungs if inhaled. Federal law requires this type of product to have child-resistant packaging.

    SeriousCPSCJul 16, 2026Gudebo

  • Panasonic NB-G200 toaster ovens recalled for shock and fire risk

    Sold nationwide. The power cord on Panasonic Model NB-G200 electric toaster ovens may not be adequately insulated due to a protective fiberglass sleeve that doesn't cover it properly. This can create a risk of electric shock or fire. Four consumers have reported tripped circuit breakers or outlets, but no fires or injuries have occurred so far.

    SeriousCPSCJul 16, 2026Panasonic

  • Oitnlaughter projecting finger lights recalled for battery ingestion risk

    Sold nationwide. These LED finger lights contain button cell batteries that children can easily access and swallow. Swallowing these batteries can cause serious internal injuries, including chemical burns, and can be fatal.

    SeriousCPSCJul 16, 2026Delightmi

  • High Valley Orchard chocolate raisins recalled for undeclared peanut

    Sold nationwide. High Valley Orchard Chocolate Covered Raisins (15oz bags, UPC 0 952348 80170 0, Lot #0160933, Best by Jan 23 2027) were packaged with undeclared peanuts due to a packaging error. The label lists only milk and soy, but the product may contain peanuts, which poses a serious risk to people with peanut allergies.

    SeriousFDAJul 15, 2026High Valley Orchard

  • Greenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batteries Due to Risk of Serious Injury from Fire Hazard

    Sold nationwide. Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit, posing a risk of serious injury from fire hazard.

    CPSCJul 9, 2026Greenworks Tools

  • Flaunt MagSafe power banks recalled for fire and burn risk

    Sold nationwide. The lithium-ion battery in Flaunt MagSafe Battery Chargers (Model E33A) can overheat and catch fire. The company has received five reports of fires, including two burn injuries. About 1,400 units were sold online from May 2024 through April 2025.

    SeriousCPSCJul 9, 2026Flaunt

  • WonderStone infant walkers recalled for fall hazard risk

    Sold nationwide. WonderStone infant walkers can fit through standard doorways and fail to stop at the edge of a step, violating the mandatory safety standard for infant walkers. This poses a risk of serious injury or death from falls.

    SeriousCPSCJul 9, 2026Wonder Stone Toys

  • Moodooy bed rails recalled for entrapment risk

    Sold nationwide. Moodooy adult portable bed rails can trap users between the rail and mattress, creating a serious risk of asphyxiation. The rails also lack required warning labels and don't meet federal safety standards for adult bed rails.

    SeriousCPSCJul 9, 2026YUEZHANG

  • BBRKIN biometric gun safes recalled for unauthorized opening risk

    Sold nationwide. The biometric locks on these gun safes can be opened by people who aren't authorized to access them, creating a serious safety risk. The safes were sold on Amazon from 2020 to 2024 and are used to store firearms and valuables.

    SeriousCPSCJul 9, 2026Jomani

  • Best Buy Insignia gas ranges recalled for fire hazard risk

    Sold nationwide. The front knobs on certain Insignia gas ranges can be accidentally turned on by people or pets, creating a risk of fire. Best Buy is offering free knob covers to prevent accidental activation. No injuries have been reported so far.

    SeriousCPSCJul 9, 2026Best Buy

  • Cuisinart Propel+ gas grill recalled for laceration risk

    Sold nationwide. The tempered glass window on the pizza oven of this grill can shatter during use, creating a laceration hazard. Conair has received 37 reports of the glass shattering and one report of fire; no injuries have been reported so far.

    SeriousCPSCJul 9, 2026Cuisinart

  • Zimmer Biomet A.T.S 4000 tourniquet hoses recalled for sterility risk

    Sold nationwide. Zimmer Biomet is recalling two A.T.S 4000 TS tourniquet system hoses because the sealing area of the sterile pouch may be breached. If used, the hose may cause a moderate, localized infection. If found before use, surgery may be briefly extended while another device is located.

    ModerateFDAJul 8, 2026Zimmer Biomet2 products

  • GORE TAG thoracic endoprosthesis recalled for catheter separation

    Sold nationwide. W L Gore & Associates has recalled specific batches of the GORE TAG Thoracic Branch Endoprosthesis Side Branch Component due to a risk of catheter separation during use. This is a surgical implant used to repair certain aortic conditions. The separation could potentially affect the device's ability to function as intended.

    ModerateFDAJul 8, 2026Gore

  • Masimo Radius VSM devices recalled for false alarms, skin irritation

    Sold nationwide. Masimo is recalling two Radius VSM products: an ECG pre-connected electrode set and disposable blood pressure cuffs, covering 1,800 units in total. The ECG feature may incorrectly flag abnormally slow or fast heart rates in patients with normal rhythms, which could distract clinicians from true alarms and delay treatment. The blood pressure cuffs may have rough edges that can cause skin irritation or redness. No injuries have been reported.

    ModerateFDAJul 8, 2026Masimo Corporation2 products

  • Laborie Solar GI System recalled for moisture accumulation risk

    Sold nationwide. Laborie Medical Technologies' Solar GI System water perfusion devices may accumulate moisture inside tubing, filters, and pressure sensors during extended clinical use. This moisture buildup can affect how the system measures airflow and pressure, potentially impacting test results.

    ModerateFDAJul 8, 2026Laborie Medical Technologies Corp

  • Bard catheters and trays recalled for lidocaine ampoule concerns

    Sold nationwide. Bard Access Systems is recalling 14 products, including PICC, midline, and dialysis catheters and biopsy trays. The recall stems from lidocaine ampoules that were made under deficient manufacturing practices, and the supplier is recalling them. No injuries have been reported.

    ModerateFDAJul 8, 2026Bard14 products

  • Covidien Shiley decannulation plug recalled for mislabeled DEHP

    Sold nationwide. The Shiley Disposable Decannulation Plug (DDCP), a red connector used on tracheostomy tubes to block airflow, carries labeling that incorrectly indicates it does not contain DEHP (a chemical compound). The product actually contains 30–35% DEHP. Users relying on the label may not be aware of DEHP exposure during use.

    ModerateFDAJul 8, 2026Covidien LLC

  • Zeiss Intrabeam radiation applicator recalled for manufacturing defect

    Sold nationwide. Certain Zeiss Intrabeam Spherical Applicator 1.5 cm units used in intraoperative radiation therapy did not meet manufacturing specifications. A total of 13 units were affected across the United States, Puerto Rico, and several other countries. No injuries have been reported.

    ModerateFDAJul 8, 2026Carl Zeiss Meditec

  • Siemens ARTIS icono ceiling monitor recalled for loose screws

    Sold nationwide. Siemens has identified a potential issue with the Display ceiling suspension (DCS Fix XL) component on ARTIS icono ceiling systems. Over time, screws that secure the monitor to the suspension may gradually loosen, which could affect the stability of the mounted display.

    ModerateFDAJul 8, 2026Siemens

  • RayCare 2024A SP1 recalled for beam note data loss risk

    Sold nationwide. RayCare 2024A SP1 oncology information system has a software issue where beam set delivery notes can lose data if modified at the same time or updated during an active treatment session. Users may not be notified when these changes occur, potentially affecting treatment records.

    ModerateFDAJul 8, 2026Raysearch Laboratories2 products

  • Accuray Cyberknife recalled for collimator fall risk

    Sold nationwide. In some cases, the collimator (a precision component) may not fully dock into the Cyberknife treatment system. This triggers a safety interlock that blocks motion from the operator console. However, if staff enter the treatment room and use the in-room control pendant to move the system, the collimator can release and fall from its housing, creating a potential impact hazard.

    ModerateFDAJul 8, 2026Accuray Incorporated

  • Siemens ARTIS icono systems recalled for loss of movement risk

    Sold nationwide. Siemens is recalling three models of its ARTIS icono imaging systems, 234 units in total, because the detector lift may stop moving after it is adjusted to its highest or lowest height limit. No injuries have been reported.

    ModerateFDAJul 8, 2026Siemens3 products

  • Accuray Cyberknife recalled for collimator drop risk

    Sold nationwide. In some cases, the collimator (a precision component) may not fully dock into the Cyberknife system. If operators bypass the safety interlock by using the in-room control pendant, the collimator can release and fall from the machine housing. This affects 48 Cyberknife units worldwide running software version 11X or earlier.

    ModerateFDAJul 8, 2026Accuray Incorporated

  • Pilling Wecksorb Neurosponges recalled for endotoxin contamination

    Sold nationwide. Pilling Wecksorb Neurosponges—sterile cotton sponges used during brain and spine surgery—may contain higher-than-safe levels of endotoxins (bacterial toxins). The affected sponges were manufactured between 2021 and 2024. No injuries have been reported, but elevated endotoxins could trigger an inflammatory response during surgery.

    ModerateFDAJul 8, 2026TELEFLEX LLC

  • Baxter operating table adapter recalled for loosening risk

    Sold nationwide. The Adapter for Head Positioning (Model 1739994) used with Baxter operating tables may become loose during patient positioning and move unintentionally. This affects 13 units distributed worldwide, primarily in Minnesota, Maryland, Pennsylvania, Canada, and numerous other countries.

    ModerateFDAJul 8, 2026Baxter

  • Boston Scientific CRE balloon catheters recalled for sterile packaging breach

    Sold nationwide. Boston Scientific is recalling 12 sizes of its CRE and CRE Pro Wireguided balloon catheters because the pouches they are packaged in may not keep the devices sterile. The recall covers 81,543 units per product and was distributed in the US and many other countries. No injuries have been reported.

    ModerateFDAJul 8, 2026Boston Scientific12 products

  • Hamilton Medical IntelliCuff recalled for motor malfunction risk

    Sold nationwide. The IntelliCuff portable cuff pressure controller may display a "Cuff System Leakage" error and cause the motor to pump continuously instead of maintaining the pressure set by the user. This can prevent the device from working as intended.

    ModerateFDAJul 8, 2026Hamilton Medical AG

  • Medtronic Harmony delivery catheter recalled for possible tip detachment

    Sold nationwide. Certain lots of the Medtronic Harmony Delivery Catheter System may have a manufacturing defect that increases the risk of the distal tip detaching from the delivery system during use. This could occur under specific procedural or anatomical conditions. About 1,881 units worldwide are affected.

    SeriousFDAJul 8, 2026Medtronic Heart Valves Division

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