Hawaii recalls

1,894 federal recalls affecting Hawaii in the last 12 months: 46 sold in Hawaii plus 1,848 sold nationwide. From the CPSC, FDA, USDA and NHTSA.

Recent recalls

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  • Stop using Koven BiDop 3 Pocket Doppler

    Sold nationwide. Koven Technology's BiDop 3 Pocket Doppler ultrasound device was distributed with labeling that claims it can be used for fetal applications, but the FDA never approved it for that use. The device is only cleared to detect blood flow in blood vessels, not for fetal monitoring. Using it for unapproved purposes could lead to incorrect results or missed diagnoses.

    ModerateFDAApr 1, 2026Koven Technology

  • Stop using Orthalign Drill Plate component

    Sold nationwide. Orthalign drill plates (Trimax-Pegged, Sizes 1–5, REF 402566) in one lot may have been made outside specifications. This could cause bone cuts larger than intended during knee surgery. Seven units were distributed in Utah.

    ModerateFDAApr 1, 2026Orthalign2 products

  • Philips ultrasound transducers recalled for unclear useful-life labeling

    Sold nationwide. Philips is recalling 11 ultrasound transducer models to clarify and update labeling that defines how long these devices are expected to remain in use. The recall was filed for clarification, and no injuries have been reported.

    FDAApr 1, 2026Philips11 products

  • Philips Trilogy Evo ventilators recalled for breath volume risk

    Sold nationwide. Philips is recalling four Trilogy ventilator models running software version 1.05.15.00: Trilogy Evo, Trilogy Evo O2, Trilogy EV300, and Trilogy Evo Universal. When non-pneumatic nebulizers are used with these ventilators, the breath volume the patient receives may differ from the amount the device is set to deliver. No injuries have been reported. The recall covers about 113,717 units per model and was distributed nationwide and in many other countries.

    SeriousFDAApr 1, 2026Philips4 products

  • Olympus endoscope valves and reprocessors recalled over compatibility issue

    Sold nationwide. Olympus is recalling four endoscope products because the MAJ-1443 and MAJ-1444 valves are no longer compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. The recall covers about 139,000 units across the US, and no injuries have been reported.

    ModerateFDAApr 1, 2026Olympus4 products

  • Stop using Beckman Coulter MicroScan Neg MIC 56

    Sold nationwide. Beckman Coulter has recalled MicroScan Neg MIC 56 antimicrobial susceptibility testing panels (Catalog C42464, Lot 2026-01-03) due to potential contamination in the test wells. These panels are used by laboratories to identify bacteria and test antibiotic resistance. Contaminated panels could produce inaccurate test results.

    ModerateFDAApr 1, 2026Beckman Coulter

  • I.T.S. bone plates and screws recalled for MRI heating risk

    Sold nationwide. I.T.S. is recalling 17 orthopedic implant product lines, including bone plates and screw systems. Updated MRI safety testing found that these implants can heat up more during certain MRI conditions than the product instructions previously stated. No injuries have been reported.

    ModerateFDAApr 1, 2026I.T.S17 products

  • Stop using affected GE Imactis CT-Navigation systems

    Sold nationwide. GE Medical Systems' Imactis CT-Navigation System (Models E85101LA and E85101LP) has a potential issue where the needle's simulated path shown to the doctor may not match where the needle actually goes during CT-guided procedures. This discrepancy could affect the accuracy of needle placement during medical procedures. No injuries have been reported.

    ModerateFDAApr 1, 2026GE

  • Handy Solutions heating pad recalled for possible burn risk

    Sold nationwide. The Handy Solutions Neck & Shoulders Heating Pad (model 25607) can overheat and cause burns if folded while in use or placed under your body. When folded, the device's safety temperature sensor cannot detect the excessive heat, so it does not shut off. The pad may emit a burning smell before melting or catching fire.

    SeriousFDAApr 1, 2026Navajo Manufacturing

  • Merit Medical catheters, sheath introducers recalled for splitting defect

    Sold nationwide. Merit Medical is recalling five products, including CentrosFLO and DuraMax dialysis catheters and 16F dual valved splittable sheath introducers. The sheath introducer may not split as intended, which can cause bleeding, pieces left in the body, procedure delays, or blood clots. No injuries have been reported.

    SeriousFDAApr 1, 2026Merit Medical5 products

  • Erbe flexible cryoprobes recalled for probe rupture risk

    Sold nationwide. Erbe is recalling three models of flexible cryoprobes used in surgery because the probes may rupture or burst during activation. The recall covers about 40,900 units sold nationwide, including Puerto Rico. No injuries have been reported.

    SeriousFDAApr 1, 2026Erbe3 products

  • Nuts.com Espresso Malted Milk Balls recalled for undeclared wheat

    Sold nationwide. Nuts.com Espresso Malted Milk Balls contain wheat and soy allergens that are not listed on the package label. The ingredient soy lecithin contains soy, and wheat is also present in the product. People with wheat or soy allergies could have a serious reaction if they eat this product.

    SeriousFDAApr 1, 2026Nuts.com

  • Sunflour Bakery hamburger buns recalled for undeclared sesame

    Sold nationwide. Sunflour Bakery hamburger buns contain sesame seeds that are not listed on the package label. One 18-ounce bag (UPC 832971001522) with an expiration date of 02/24/2026 was distributed to a retailer in Orange County. People with sesame allergies could have a serious reaction if they eat these buns.

    ModerateFDAApr 1, 2026Sunflour Bakery

  • Bulk packaged Colustrum Powder. packaged with generic product label.

    Sold nationwide. Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.

    FDAApr 1, 2026Herbal Creations USA

  • First Street and Treasured Harvest peanuts recalled for glass

    Sold nationwide. Western Mixers is recalling two sizes of Chilli Spanish Peanuts because glass was found inside sealed containers. The products are sold under the First Street brand (11 oz containers) and the Treasured Harvest brand (25 lb bags). No injuries have been reported. The recall was sent to two businesses with a total of 53 retail locations nationwide.

    ModerateFDAApr 1, 2026First Street2 products

  • Stop using recalled Meclizine Hydrochloride tablets

    Sold nationwide. American Health Packaging is recalling specific batches of Meclizine Hydrochloride 12.5 mg tablets because they failed to meet required tablet specifications. The affected product is Lot #1024852 with an expiration date of 9/30/2026. No injuries have been reported.

    ModerateFDAApr 1, 2026Amerisource

  • Stop using Teva Octreotide Acetate injection

    Sold nationwide. Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension due to sterility concerns identified at the manufacturing facility. The FDA found quality system deficiencies that could affect the safety of the medication.

    ModerateFDAApr 1, 2026Teva3 products

  • Macleods levothyroxine tablets recalled for subpotency

    Sold nationwide. Macleods Pharma USA is recalling Levothyroxine Sodium Tablets USP 150 mcg because they may contain less active ingredient than labeled. This means the medication may not work as intended to treat thyroid conditions. The affected lot is 16240062A with an expiration date of March 2026.

    ModerateFDAApr 1, 2026MacLeods Pharma

  • Stop using recalled CUROSURF lung surfactant

    Sold nationwide. Chiesi USA is recalling specific lots of CUROSURF, a medication given to premature infants to help them breathe. The company cannot confirm that all vials are sterile, which means they may be contaminated. No infections have been reported so far.

    ModerateFDAApr 1, 2026Chiesi

  • Stop using Radnostix Gelatin Capsule Pack

    Sold nationwide. Radnostix Gelatin Capsule Packs used with Sodium Iodide I-131 Kit have failed quality specifications. The affected capsules may not perform as intended. Three specific lots distributed nationwide are involved.

    ModerateFDAApr 1, 2026Radnostix

  • Kian Pee Wan capsules recalled for undeclared dexamethasone

    Sold nationwide. Kian Pee Wan capsules, sold online as a dietary supplement for weight gain and appetite, contain two hidden prescription drugs: dexamethasone (a corticosteroid) and cyproheptadine (an antihistamine). These drugs were not listed on the label. Taking these undeclared drugs can cause serious health problems including infections, high blood sugar, psychiatric issues, and withdrawal symptoms if stopped abruptly.

    SeriousFDAMar 30, 2026Buy-herbal.com

  • MPINOI bed rails recalled for entrapment and asphyxiation risk

    Sold nationwide. MPINOI brand adult 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. About 200 units were sold on Amazon between December 2025 and February 2026.

    SeriousCPSCMar 26, 2026Bioenrrty

  • DIY Cold Plunge sauna heater kits recalled for fire risk

    Sold nationwide. The electrical components in DIY Cold Plunge Sauna Heater Kits can overheat and create a fire hazard. The company has received 12 reports of units overheating, though no fires or injuries have occurred yet. The kits were sold online from March 2025 through February 2026.

    SeriousCPSCMar 26, 2026DIY Cold Plunge

  • FUNTOK ride-on trucks recalled for fire and burn hazards

    Sold nationwide. FUNTOK 24V 2-Seater Ride-On Trucks (model DLS-K03) can overheat and catch fire due to a defective circuit board. The company has received 11 reports of fires, sparking, and smoking. No injuries have been reported yet, but the risk of serious burn injury is significant.

    SeriousCPSCMar 26, 2026Segmart

  • Petzl Nomic and Ergonomic ice axes recalled for fall hazard

    Sold nationwide. The aluminum shaft on Petzl Nomic and Ergonomic ice climbing axes can break at the handle during use, creating a fall hazard. This affects axes sold between December 2017 and March 2022. Petzl has received 26 reports of shaft breaks but no injuries so far.

    SeriousCPSCMar 26, 2026Petzl

  • CCCEI power strips recalled for fire risk when overloaded

    Sold nationwide. CCCEI-branded power strips sold online lack proper safety protection and can overheat and catch fire if too many devices are plugged in. Two units have already sparked and melted. The company is recalling about 5,500 units sold between April 2024 and January 2026.

    SeriousCPSCMar 26, 2026Middle Way Electronics

  • GLMZZ fidget magnet toys recalled for magnet ingestion risk

    Sold nationwide. GLMZZ Fidget Magnet Ball Toy Sets contain high-powered magnets that can be swallowed by children. If multiple magnets are ingested, they can attract each other inside the digestive system, causing perforations, blockages, or twisting of the intestines—which can lead to serious injury or death. The sets were sold on Amazon between February and October 2025.

    SeriousCPSCMar 26, 2026GLMZZ

  • Sunnyyes LED mini lights recalled for coin battery ingestion risk

    Sold nationwide. Sunnyyes LED mini lights contain lithium coin batteries that children can easily access and swallow. The battery compartment screws can come loose, and the packaging lacks required safety warnings. Swallowing these batteries can cause serious internal burns and death.

    SeriousCPSCMar 26, 2026Sunnyyes

  • DuraTrac gas connectors recalled for potential fire hazard

    Sold nationwide. DuraTrac stainless steel gas connectors sold between May and November 2025 contain a manufacturing defect that can cause gas leaks. These leaks pose a fire hazard. About 196,800 units are affected.

    SeriousCPSCMar 26, 2026DuraTrac

  • AirClub convertible bassinets recalled for infant fall hazard

    Sold nationwide. AirClub convertible bassinets (model QX-831) have a defective attachment mechanism that creates a dangerous gap between the bassinet and adult bed mattress. Infants can fall through this opening, causing serious injury or death. About 110,400 units were sold online between October 2023 and December 2025.

    SeriousCPSCMar 26, 2026AirClub

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