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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  • Philips Trilogy Evo ventilators recalled for delayed alarm

    Sold nationwide. Philips is recalling four Trilogy ventilator models running Software Version 1.05.15.00, covering 113,717 units in total. In some situations, the Obstruction Alarm does not sound within the time required by applicable standards and may take up to four breaths to trigger. No injuries have been reported.

    SeriousFDAApr 8, 2026Philips4 products

  • Abiomed Impella Controller recalled for possible delayed alarm

    Sold nationwide. Abiomed's Impella Controller may display a delayed "Purge System Blocked" alarm when used with first-generation Impella 5.5 pumps. This could prevent timely detection of a blocked purge system. The issue affects 62 controllers with specific serial numbers in software versions 8.2.2 through 8.5.

    SeriousFDAApr 8, 2026Abiomed

  • Abiomed Impella Generation 1 purge cassettes recalled for leak risk

    Sold nationwide. Abiomed is recalling purge cassettes used in Impella heart pump systems because Generation 1 cassettes have an increased risk of leaking during use. This affects multiple Impella pump models sold globally, with specific batch numbers identified from 2024.

    SeriousFDAApr 8, 2026Abiomed

  • Imu-Tek Colostrum-5 supplements recalled for possible under-processing

    Imu-Tek Animal Health is recalling two products: Imu-Tek Colostrum-5 120-capsule bottles and Imu-Tek Colostrum-5 powder bottles. The company says the product may not have been fully processed. No injuries have been reported.

    ModerateFDAApr 8, 2026Imu-Tek2 products

  • Lone Star Dairy spray dried dairy powder recalled for Salmonella

    Sold nationwide. Lone Star Dairy Products LLC is recalling spray dried milk powder products because Salmonella bacteria was found during testing of finished products. The recall affects specific lot codes of NFDM Low Heat, NFDM High Heat, and SMP Medium Heat products sold in 25 kg bags and 1 metric ton totes.

    SeriousFDAApr 8, 2026Lone Star Dairy Products

  • Cheetos and Loaded dumplings recalled for possible glass

    JFE Franchising is recalling five dumpling products that may contain pieces of glass. The products are sold as Cheetos Flamin' Hot Loaded Dumpling, plus Dumpling Vegetable, Loaded Dumpling Vegetable and Dumpling Party Tray items. No injuries have been reported.

    ModerateFDAApr 8, 2026JFE Franchising2 products

  • Amneal magnesium sulfate IV bag recalled for tranexamic acid mix-up

    Sold nationwide. Some cartons of Amneal Magnesium Sulfate IV bags were mislabeled and contained Tranexamic Acid (a different medication) instead. This mix-up affects lot AH250162 with an expiration date of 8/31/2027. The error was discovered before the product reached patients.

    SeriousFDAApr 8, 2026Amneal Pharmaceuticals

  • Appco Pharma prazosin capsules recalled for nitrosamine impurity

    Sold nationwide. Appco Pharma LLC is recalling prazosin hydrochloride 1mg capsules (100-count bottles) because they may contain higher-than-acceptable levels of a nitrosamine impurity. This impurity was detected during manufacturing quality checks. The recall affects specific lot numbers distributed nationwide.

    ModerateFDAApr 8, 2026Appco Pharma3 products

  • Walgreens, Good Sense and more eye drops recalled for sterility

    Sold nationwide. K.C. Pharmaceuticals is recalling eight sterile eye drop products because the company cannot confirm they are sterile. The drops were sold under store and pharmacy brands including Best Choice, Walgreens, GERI CARE, LEADER, Good Sense, Industrial Eye Relief and Rugby. No injuries have been reported.

    ModerateFDAApr 8, 2026K.C. Pharmaceuticals8 products

  • Amneal tramadol tablets recalled for impurity out of specification

    Sold nationwide. Amneal Pharmaceuticals is recalling specific lots of tramadol 50 mg tablets because they contain higher-than-allowed levels of a chemical impurity called N-nitroso-desmethyl-tramadol (NDSRI). The impurity was discovered during stability testing of tablets nearing the end of their shelf life. No injuries have been reported.

    ModerateFDAApr 8, 2026Amneal Pharmaceuticals

  • Alembic bromfenac eye drops recalled for failed impurity testing

    Sold nationwide. Alembic Pharmaceuticals is recalling specific lots of Bromfenac Ophthalmic Solution 0.07% because the medication failed purity and degradation tests during stability testing at 20 months. The affected eye drops may contain higher-than-acceptable impurity levels, which could affect safety and effectiveness.

    ModerateFDAApr 8, 2026Alembic Pharmaceuticals

  • Good Brain Tonic recalled for potential botulism

    Sold nationwide. Liquid Blenz Corp. is recalling all Good Brain Tonic beverages (16 oz and 32 oz bottles) due to a potential botulism risk. Botulism is a serious form of food poisoning. No illnesses have been reported yet, but the product was distributed nationwide.

    SeriousFDAApr 6, 2026Liquid Blenz

  • RAW FARM raw cheddar cheese recalled for potential E. coli

    Sold nationwide. Raw Farm has recalled specific batches of raw cheddar cheese products (blocks and shredded) due to a potential link to an E. coli O157:H7 outbreak. The recall includes multiple batch numbers and expiration dates listed on the Raw Farm website. No pathogens have been found in Raw Farm products tested so far.

    SeriousFDAApr 2, 2026

  • Universal Broadmoor canopy bed frames recalled for collapse risk

    Sold nationwide. The canopy beams on certain Samson International bed frames can collapse, especially when the bed is moved. The company has received five reports of the canopy collapsing and striking people, resulting in shoulder and head injuries.

    SeriousCPSCApr 2, 2026Samson

  • Tuymec minoxidil hair spray recalled for child poisoning risk

    Sold nationwide. Tuymec Minoxidil Hair Growth Spray bottles sold on Amazon do not have child-resistant caps, violating federal safety rules. Minoxidil is toxic if swallowed by young children and can cause serious injury or death.

    SeriousCPSCApr 2, 2026DrHealBeauty

  • Member's Mark children's pajama sets recalled for burn risk

    Sold nationwide. Sam's Club is recalling Member's Mark Valentine-themed children's pajama sets because they don't meet mandatory flammability standards for sleepwear. This poses a risk of burn injuries. About 18,000 sets were sold online between December 2025 and January 2026.

    SeriousCPSCApr 2, 2026Hansoll Textile

  • HTRC and Haisito T400 battery chargers recalled for fire risk

    Sold nationwide. HTRC and Haisito brand T400 battery chargers can overheat and ignite, causing fires or explosions. The company has received 33 reports of fires and explosions, including three reports of injuries from burns and smoke inhalation.

    SeriousCPSCApr 2, 2026Haitan

  • Sangohe bed rails recalled for entrapment and asphyxiation risk

    Sold nationwide. Sangohe portable bed rails (models 504E and 504Q) can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 36,500 units were sold online starting August 2023.

    SeriousCPSCApr 2, 2026Zhongshan KDB Health Solutions

  • Granitestone Diamond Pro pans recalled for impact and burn hazards

    Sold nationwide. The metal cap on the handle screw of these sauté pans can detach and eject forcefully when the pan is heated. E Mishan has received at least 98 reports of the cap detaching, including one case where a consumer was bruised and burned.

    SeriousCPSCApr 2, 2026Mishan

  • TecFlox hair and beard serum recalled for child poisoning risk

    Sold nationwide. TecFlox minoxidil topical solution bottles do not have child-resistant packaging as required by law. The liquid inside can cause serious injury or death if a young child swallows it. About 900 bottles were sold on Amazon in October 2025.

    SeriousCPSCApr 2, 2026TecFlox

  • ELENKER portable bed rails recalled for entrapment and asphyxiation risk

    Sold nationwide. ELENKER portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. The recalled models are silver collapsible rails sold on Amazon since August 2023.

    SeriousCPSCApr 2, 2026Shiahaha

  • Ocun Condor HMS carabiners recalled for gate malfunction risk

    Sold nationwide. OCUN NA is recalling certain Condor HMS Triple Carabiners sold from February 2025 through February 2026. The carabiner's gate can fail to close automatically and may require manual closing, which could cause the carabiner to fail during climbing and lead to a fall.

    SeriousCPSCApr 2, 2026OCUN

  • Coluans Christmas light-up rings recalled for button battery ingestion risk

    Sold nationwide. These Christmas light-up party favors contain button cell batteries that children can easily access and swallow. Swallowed button batteries can cause serious internal burns and death. The rings were sold on Amazon between August and December 2025.

    SeriousCPSCApr 2, 2026BUDI

  • Gavoyeat Halloween light-up rings recalled for battery ingestion risk

    Sold nationwide. These Halloween light-up rings contain easily accessible button cell batteries that children can remove and swallow. Swallowed button batteries can cause serious internal burns and death within hours. About 800 units were sold on Amazon between June 2025 and January 2026.

    SeriousCPSCApr 2, 2026CSZWEICD

  • Beestech spiral tower toys recalled for choking hazard

    Sold nationwide. Beestech spiral tower toys sold on Amazon contain small plastic balls and are marketed for children under 3 years old, violating federal toy safety rules. The small balls pose a serious choking hazard. About 200 units were sold between November and December 2025.

    SeriousCPSCApr 2, 2026Beestech

  • Stop using Medline Puracol wound dressings

    Sold nationwide. Medline Industries has recalled specific lots of Puracol and Puracol Plus collagen wound dressings due to elevated endotoxin levels. These contaminants can cause inflammation, tissue irritation, delayed healing, fever, low blood pressure, and in severe cases, septic shock.

    SeriousFDAApr 1, 2026Medline

  • Check BD Alaris System network security requirements

    Sold nationwide. The labeling on BD Alaris System with Guardrails Suite MX does not specify which version of Transport Layer Security (TLS) must be enabled on hospital networks for secure Wi-Fi communication with Point-of-Care Units. This could create confusion during setup and potentially leave devices with inadequate security settings.

    ModerateFDAApr 1, 2026CareFusion

  • Olympus cutting forceps recalled for jaw breakage risk

    Sold nationwide. Olympus is recalling seven models of bipolar and PK/PKS cutting forceps, 3,788 units in total, used in medical procedures. The supplier did not adequately validate a welding process for components, and defective welds could cause the forceps' jaw to break during clinical use. No injuries have been reported.

    ModerateFDAApr 1, 2026Olympus7 products

  • Tandem insulin pumps recalled for Czech guide translation errors

    Sold nationwide. Tandem Diabetes Care insulin pumps distributed in the Czech Republic and Slovakia have translation errors in their Czech language user guide. The most serious error tells users to verify the infusion set is connected to the body when it should say the opposite—that it should NOT be connected. Following these incorrect instructions could cause unintended insulin delivery and dangerously low blood sugar.

    ModerateFDAApr 1, 2026Tandem Diabetes Care

  • MiniMed 780G pump software recalled for insulin delivery risk

    Sold nationwide. Medtronic has recalled certain MiniMed 780G insulin pumps due to software defects that can cause the pump to deliver too much insulin, too little insulin, or stop delivering insulin entirely. These defects appeared after software updates (versions 6.60, 6.61, and 6.62) and may result in dangerously high or low blood sugar levels. The recall affects over 26,000 pumps with specific serial numbers.

    SeriousFDAApr 1, 2026Medtronic

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Alaska Recall List — Page 42 | Recall Weekly