Hawaii recalls

1,920 federal recalls affecting Hawaii in the last 12 months: 46 sold in Hawaii plus 1,874 sold nationwide. From the CPSC, FDA, USDA and NHTSA.

Recent recalls

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  • Jerify magnetic toy sets recalled for magnet ingestion risk

    Sold nationwide. These 30-piece magnetic toy sets contain high-powered magnets in the hands and feet that can come loose and be swallowed by children. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious injuries including intestinal perforation, blockage, and blood poisoning. Two children have already been hospitalized after removing and swallowing magnets from these toys.

    SeriousCPSCSep 17, 2026Colerinsec

  • Charbroil Bistro Pro electric grills recalled for electric shock risk

    Sold nationwide. The grounding wire inside these electric grills can disconnect from the heating element, which removes a safety layer that normally protects against electric shock. This affects specific models made between October and December 2025. No injuries have been reported.

    ModerateCPSCSep 17, 2026Char-Broil

  • Windstone Medical AMS Convenience Kit recalled for detached port parts

    Sold nationwide. Windstone Medical Packaging's AMS Convenience Kit DSAEK Pack contains saline solution bags with blue connector pieces that may detach from the infusion port during normal use. This could allow contamination or improper fluid delivery during ophthalmic surgery.

    SeriousFDASep 16, 2026Windstone Medical Packaging

  • Nipro MedicaLyte and Citric Complete dialysis concentrates recalled for endotoxin

    Sold nationwide. Nipro is recalling four hemodialysis concentrate products because they may contain high levels of endotoxin, a substance from bacteria. The recall covers about 13,000 cases and 100 drums across the US, Guatemala, and Panama, with US distribution in FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA. No injuries have been reported.

    SeriousFDASep 16, 2026Nipro4 products

  • HeartSine defibrillators recalled for electrical fault risk

    Sold nationwide. HeartSine Technologies has recalled certain models of the SAM 350P, SAM 360P, and SAM 450P public access defibrillators (PADs) due to a damaged membrane component that can cause an intermittent electrical fault. The fault could prevent the device from operating properly when needed in a cardiac emergency. Approximately 11,912 affected units have been identified by serial number.

    SeriousFDASep 16, 2026HeartSine

  • Bard catheter trays recalled for contaminated pericare wipes

    Sold nationwide. Bard is recalling six Foley and intermittent catheter tray products because the pericare wipes packed with them may have contamination on their surface. The recall followed customer complaints, and no injuries have been reported. The trays were distributed across the United States and in several other countries.

    ModerateFDASep 16, 2026Bard6 products

  • Getinge PVC thoracic catheters recalled for bacterial endotoxin

    Sold nationwide. Atrium Medical is recalling three Getinge PVC thoracic catheter products, covering 11 model sizes, from a single lot. Testing found bacterial endotoxin levels above the allowed limit. No injuries have been reported.

    ModerateFDASep 16, 2026Atrium Medical3 products

  • Lutronic DermaV laser system recalled for burn risk

    Sold nationwide. Lutronic's DermaV laser system may produce sparks and loud noise when used at higher energy levels (fluences) at the 1064 nm wavelength with current cooling settings. This spark hazard could result in patient burns during treatment.

    ModerateFDASep 16, 2026Lutronic

  • Halyard IV Start Kit recalled for seal integrity issue

    Sold nationwide. Halyard IV Start Kit Non-Sterile (REF: KRIV26-02) convenience kits contain BD ChloraPrep Clear and FREPP Clear applicators with wrinkles in the paper lidding that may breach the seal. This compromises sterility assurance of the applicators. 98 kits in lot 1658438 (expiration 7/31/2026) were distributed nationally.

    ModerateFDASep 16, 2026AVID MedicalExpanded Sep 30

  • Given Imaging Bravo CF capsule devices recalled for possible detachment

    Sold nationwide. The Bravo CF capsule delivery device is used during esophageal pH monitoring procedures to attach a small capsule to the esophagus. The capsule may fail to attach properly or detach from the delivery device during use. This can result in the capsule being inhaled, perforating the esophagus, blocking the airway, or causing bleeding.

    SeriousFDASep 16, 2026Given Imaging

  • International Specialty Supply alfalfa recalled for possible E. coli, Salmonella

    International Sprout Holdings' alfalfa product (50 lb. bags, Lot SAL2-24JB) has been recalled due to potential E. coli and Salmonella contamination. The affected product was distributed wholesale to food service operators and retailers across 16 U.S. states, Puerto Rico, Canada, Mexico, Tahiti, and Venezuela.

    SeriousFDASep 16, 2026International Specialty Supply

  • Prolon almond and cocoa spread recalled for undeclared tree nuts

    Sold nationwide. L-Nutra Inc's Prolon Everyday Apulian Almond & Cocoa Spread contains undeclared hazelnut, cashew, and pistachio allergens. The product was sold online nationwide in 8-ounce glass jars (Lot L2755, expiring January 2, 2027).

    ModerateFDASep 16, 2026Prolon

  • Momchipz Gluten Free Veggie Chips recalled for undeclared wheat

    Sold nationwide. Momchipz Gluten Free Veggie Chips (Broccoli Florets & Cauliflower, 3 oz) contain undeclared wheat, which is not listed on the package label. The product was sold in the U.S. and imported from Indonesia. People with celiac disease or wheat allergy are at risk.

    SeriousFDASep 16, 2026Momchipz

  • B. Braun sodium chloride injection recalled for particulate matter

    Sold nationwide. B. Braun Medical Inc. is recalling specific lots of 0.9% Sodium Chloride Injection due to the presence of particulate matter, including iron oxide, inorganic material, cellulose fibers, and polystyrene. The contamination was identified during quality testing. This is a sterile injectable product distributed nationwide.

    SeriousFDASep 16, 2026B. Braun

  • American Regent epinephrine vials recalled for particulate and sterility concerns

    Sold nationwide. American Regent's epinephrine injection (1 mg/mL, 30 mL vials) may contain particulate matter—including nylon, glass, and other materials—and some vials are broken or leaking. This affects the sterility and safety of the medication. Three specific lot numbers distributed nationwide are involved.

    SeriousFDASep 16, 2026American Regent

  • OurPharma fentanyl injection recalled for expiration date mismatch

    Sold nationwide. OurPharma LLC's fentanyl citrate 1,000 mcg injection solution has conflicting expiration dates printed on the IV bag and product labeling. The bag shows expiry dates of 07/31/2026 or 11/30/2026, while the product itself is labeled as expiring 12/09/2026. This discrepancy could lead to confusion about when the medication is safe to use.

    ModerateFDASep 16, 2026OurPharma

  • Baxter Dextrose Injection recalled for stainless steel particles

    Sold nationwide. Baxter Healthcare identified stainless steel particles in certain 2000 mL bags of Dextrose Injection, USP 70%. The contamination affected 606 bags (Lot #Y495066, expiration July 31, 2027) distributed nationwide. No injuries have been reported.

    SeriousFDASep 16, 2026Baxter

  • Ajanta Pharma fluphenazine tablets recalled for impurity level

    Sold nationwide. Ajanta Pharma USA Inc. is recalling fluphenazine hydrochloride 1mg tablets (NDC 27241-255-01) because stability testing at 18 months found organic impurity levels slightly above specification limits. The tablets contained 1.1% of Impurity-A, exceeding the 1.0% specification. No injuries have been reported.

    ModerateFDASep 16, 2026Ajanta Pharma

  • ImprimisRx eye drops recalled for subpotent formulation

    Sold nationwide. ImprimisRx NJ LLC is recalling specific lots of Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution used in medical offices because the medication contains lower-than-intended active ingredients. The affected lots may not work as intended for their intended use.

    ModerateFDASep 16, 2026ImprimisRx

  • So Delicious Salted Caramel Cluster recalled for possible foreign material

    Sold nationwide. So Delicious Dairy Free® Salted Caramel Cluster Non-Dairy Frozen Dessert pints may contain small stones or other hard objects in the cashew pieces. The issue was found through customer complaints. Affected pints have best-by dates on or before April 3, 2028.

    ModerateFDASep 15, 2026So Delicious

  • bettergoods Lemon Alfredo Fettuccine recalled for possible Listeria

    Sold nationwide. Gias Foods is recalling two lots of Bettergoods Authentic Italian Lemon Alfredo Fettuccine frozen pasta because it may be contaminated with Listeria monocytogenes, a bacteria that can cause serious infections. The recall affects products sold at Walmart with lot numbers L6079C or L6080C and expiration dates of 09/19/2027 or 09/20/2027. No illnesses have been reported so far.

    SeriousFDASep 15, 2026Gias FoodsUpdated Oct 1

  • Centric Compounding glutathione, Myer's Cocktail vials recalled for elevated endotoxin

    Sold nationwide. Centric Compounding has recalled six lots of Glutathione, Myer's Cocktail, and Tri-Immune Boost injectable vials due to elevated endotoxin contamination. The company has received nine reports of adverse reactions including fever, chills, chest pain, nausea, vomiting, headache, and malaise. Elevated endotoxins in injectable products can cause serious medical events including fever, low blood pressure, inflammatory reactions, anaphylactic shock, and death.

    SeriousFDASep 11, 2026Centric Compounding

  • FJTJBSI six-drawer dressers recalled for tip-over risk

    Sold nationwide. These six-drawer wood dressers can tip over and trap children if not anchored to the wall. The dressers do not meet federal safety standards required for furniture that children could access.

    SeriousCPSCSep 10, 2026FJTJBSI

  • Triumph TF450 motorcycles recalled for engine failure crash risk

    Sold nationwide. The engine rocker arm on certain 2025 and 2026 Triumph TF450 competition motorcycles can seize or stick, causing the exhaust valves to remain open or break. This can lead to sudden loss of engine performance and increased risk of a crash. Triumph has received 12 reports of this problem, including one injury.

    SeriousCPSCSep 10, 2026Triumph

  • California Cade Electronic finger lights recalled for battery ingestion risk

    Sold nationwide. These finger light toys contain button cell batteries that children can easily access and swallow. Swallowed button batteries can cause serious internal injuries, chemical burns, and death.

    SeriousCPSCSep 10, 2026Cade

  • AGA, La Cornue ranges recalled for gas leak risk

    Sold nationwide. Certain dual fuel ranges manufactured between March 2025 and July 2026 may be missing a cap on the gas test port. This missing cap can allow gas to leak, creating a risk of fire or explosion. No injuries have been reported so far.

    SeriousCPSCSep 10, 2026AGA Rangemaster

  • Prepared Hero fire spray canisters recalled for fire failure risk

    Sold nationwide. Prepared Hero fire spray canisters can deteriorate over time and rupture, potentially failing to work during a fire. The company has received nine reports of canisters exploding or deteriorating while in storage. The affected canisters are marked with date code "09/2024" on the base.

    SeriousCPSCSep 10, 2026Prepared Hero

  • Wantefully hair dryer brushes recalled for electrocution risk

    Sold nationwide. These hair dryer brushes lack a safety device that prevents electrocution if they fall into water while plugged in. They can also overheat and cause burns. One unit was reported to overheat and melt.

    SeriousCPSCSep 10, 2026Wantefully

  • Lontcs Busy Board toys recalled for lead poisoning risk

    Sold nationwide. The zipper on Lontcs Busy Board toys contains lead levels that exceed the federal lead paint safety standard. Lead is toxic if swallowed by young children and can cause serious health problems. The toys were sold online through Amazon from May 2024 to July 2026.

    SeriousCPSCSep 10, 2026SQT

  • Sweet Cubby children's loungewear sets recalled for burn hazard

    Sold nationwide. Sweet Cubby children's loungewear sets do not meet federal flammability standards for sleepwear. The two-piece sets (short-sleeved shirt and shorts) sold online can catch fire more easily than safe sleepwear, posing a risk of serious burn injury. About 12,461 sets were sold through SHEIN.com between June 2025 and May 2026.

    SeriousCPSCSep 10, 2026Sweet Cubby

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