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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  • Kitchen HQ insulated bowls recalled for microwave fire hazard

    Sold nationwide. Metal springs in the detachable hinged lids of Kitchen HQ brand thermal insulated bowls can catch fire when used in the microwave. HSN has received 30 reports of the bowls smoking, sparking, melting, or catching fire, including one that caused property damage.

    SeriousCPSCJun 11, 2026HSN

  • Joyin Sloosh dive sticks recalled for impalement hazard

    Sold nationwide. Joyin's Sloosh dive sticks (model 40041) are too hard and can cause serious piercing injuries if children fall or land on them in shallow water. Facial and eye injuries are also possible when retrieving sticks underwater. These sticks violate federal safety standards for dive toys.

    SeriousCPSCJun 11, 2026JoyinExpanded Jul 30

  • Albertson's carrot cake recalled for undeclared pecan or walnut

    Sold nationwide. Albertsons store-made 8-inch carrot cakes were sold without proper allergen labeling. The cakes contain pecan or walnut but the labels do not declare these nuts, posing a risk to people with nut allergies. About 167 cakes with a "Packed On" date of May 5 or earlier are affected.

    ModerateFDAJun 10, 2026Albertsons121 products

  • Second Nature Keto Crunch Smart Mix recalled for possible allergens

    Sold nationwide. Second Nature Keto Crunch Smart Mix 10-ounce pouches may contain undeclared cashews, pistachios, and dried cherries. These allergens are not listed on the label, which is a serious concern for people with tree nut allergies. The product was distributed nationwide through retail stores and online.

    ModerateFDAJun 10, 2026Second Nature

  • Yunker Energy & Health supplement recalled for Vitamin E mismatch

    Sold nationwide. Sato Pharmaceutical's Yunker Energy & Health Herbal Supplement with Vitamins does not contain the amount of Vitamin E stated on its label. The affected product was distributed nationwide through two domestic distributors. No injuries have been reported.

    FDAJun 10, 2026Yunker

  • a2 Platinum infant formula recalled for possible Cereulide toxin

    Sold nationwide. The a2 Milk Company is recalling specific lots of a2 Platinum Premium infant formula powder due to possible contamination with Cereulide toxin, a substance produced by certain bacteria. The affected product was distributed nationwide in 31.7 oz metal tins. No illnesses have been reported to date.

    SeriousFDAJun 10, 2026a2

  • BD ChloraPrep and FREPP applicators recalled for fungal contamination

    Sold nationwide. BD is recalling specific lots of ChloraPrep Clear 1 mL and FREPP Clear 1.5 mL skin preparation applicators due to potential fungal contamination (Aspergillus penicillioides) that could grow under certain environmental conditions. The affected products were distributed to hospitals and medical distributors between March and June 2024.

    SeriousFDAJun 6, 2026BD

  • Target Up & Up baby wipes recalled for bacterial contamination

    Sold nationwide. Target is recalling Up & Up Fragrance Free and Fresh Cucumber Scented Baby Wipes after FDA testing found harmful bacteria (Burkholderia cepacia complex and Burkholderia gladioli) in product samples. Some customers also reported discoloration. These bacteria can cause serious infections, especially in newborns and infants with developing immune systems.

    SeriousFDAJun 4, 2026Target

  • Pearl Milling pancake mix recalled for undeclared milk, soy

    Sold nationwide. Ballester Hermanos is recalling limited packages of Pearl Milling Company Original Pancake & Waffles Complete mix (5.99 oz) sold in Puerto Rico. The label incorrectly stated "may contain" milk and soy instead of "contains" these allergens, creating a serious risk for people with allergies to these ingredients. No illnesses have been reported so far.

    SeriousFDAJun 4, 2026Pearl Milling

  • Pearl Milling pancake mix recalled for undeclared milk and soy

    Sold nationwide. Pearl Milling Company Original Pancake & Waffles mix (5.99 oz pouches) sold in Puerto Rico contains milk and soy but was labeled as "may contain" instead of "contains." People with milk or soy allergies could have a serious allergic reaction if they consume it.

    ModerateFDAJun 4, 2026Pearl Milling

  • Vornado SRTH small room tower heaters recalled for fire hazard

    Sold nationwide. The fan blade in Vornado SRTH tower heaters can detach from the motor shaft, causing the fan to slow or stop. This leads to overheating and melting of internal parts, which can ignite and cause a fire if the safety cutoff fails. Vornado has received 32 reports of overheating, including 8 fires and 1 smoke inhalation.

    SeriousCPSCJun 4, 2026Vornado

  • SUNS elevator interlock switches recalled for fall and crush risk

    Sold nationwide. The SUNS SS6291 interlock switch, used in residential elevators, can get stuck in a retracted position. When this happens, the exterior elevator door may stay unlocked even when the elevator moves to another floor, creating a risk of falling or being crushed.

    SeriousCPSCJun 4, 2026Suns

  • Boon NURSH baby bottles recalled for choking hazard

    Sold nationwide. The hard plastic outer shell on these bottles can bubble or peel, creating loose pieces of film-like plastic that a baby could choke on. The manufacturer has received 135 reports of this issue, though no injuries have been reported yet.

    SeriousCPSCJun 4, 2026Tomy

  • Broqixin pool drain covers recalled for entrapment risk

    Sold nationwide. Broqixin-branded pool drain covers do not meet federal safety standards and can trap swimmers underwater, creating a drowning hazard. The white plastic covers (Model 11064W, about 7.36 inches wide) were sold online through Amazon from January to April 2026.

    SeriousCPSCJun 4, 2026Broqixin

  • Gudook bicycle helmets recalled for head injury risk

    Sold nationwide. Gudook-branded bicycle helmets (model KY-055) do not meet mandatory safety standards for impact protection. The helmets can fail to protect your head in a crash, creating a serious injury or death risk. Only helmets with batch number 202503 and manufacture date March 2025 are affected.

    SeriousCPSCJun 4, 2026Gudook Outdoor Sports

  • Crenlux pool drain covers recalled for entrapment risk

    Sold nationwide. Crenlux pool drain covers do not meet federal safety standards and can trap swimmers or bathers underwater, creating a serious drowning hazard. The white plastic covers, about 8 inches in diameter, were sold online through Amazon from June 2025 to March 2026.

    SeriousCPSCJun 4, 2026Eicong

  • Tiny Land play tents recalled for fiberglass pole irritation risk

    Sold nationwide. Tiny Land children's play tents contain fiberglass poles that can shed fibers, causing skin and eye irritation. The company has received eight reports of fiber shedding resulting in irritation. The tents were sold online from November 2025 through March 2026.

    ModerateCPSCJun 4, 2026Tiny Land

  • Little Grape Land nursing pillows recalled for suffocation risk

    Sold nationwide. Little Grape Land nursing pillows sold on Amazon do not meet federal safety standards and can obstruct an infant's breathing. The U-shaped pillows, sold in various patterns between August 2025 and April 2026, pose a serious risk of suffocation during infant feeding or tummy time.

    SeriousCPSCJun 4, 2026Little Grape Land US

  • Wyze Solar Cam Pan recalled for fire and burn risk

    Sold nationwide. Wyze Solar Cam Pan security cameras can overheat and catch fire if installed incorrectly. The incorrect assembly instructions may lead users to accidentally puncture the lithium-ion battery's metal casing with a long, flat-head screw, causing the battery to rapidly overheat. The company has received reports of six cameras catching fire and exploding, with six consumers suffering minor burns.

    SeriousCPSCJun 4, 2026Wyze

  • Medline medical kit recalled for wrong syringe type

    Sold nationwide. Some Medline EYE TRAY-LF convenience kits (SKU DYNJ21627P) contain syringes labeled as tuberculin syringes on the box, but the actual syringes inside are insulin syringes. Using the wrong syringe type could lead to incorrect dosing.

    ModerateFDAJun 3, 2026Medline

  • Philips Azurion and Allura systems recalled for hard drive failure risk

    Sold nationwide. Philips is recalling Azurion and Allura imaging systems because the hard drives in their PCs may slow down as they age, especially after six years of use. Depending on the system, this can cause loss of imaging function, and in Allura systems it may also cause loss of motorized movement or data loss. A system restart may temporarily restore function. No injuries have been reported, and the recall covers 2 product lines with about 3,069 affected units.

    ModerateFDAJun 3, 2026Philips2 products

  • GE HealthCare ApexPro telemetry servers recalled for monitoring loss risk

    Sold nationwide. GE HealthCare recalled six ApexPro CARESCAPE Telemetry Server products and related software. A persistent NO COMM or OFF NETWORK condition at the Central Station could cause loss of ECG and SpO2 monitoring. No injuries have been reported.

    SeriousFDAJun 3, 2026GE6 products

  • Medtronic Pocket Adaptor Kit recalled for incorrect labeling

    Sold nationwide. A limited number of Medtronic 1x4 Pocket Adaptor Kits (Models 64001 and 64002) used in deep brain stimulation devices are labeled with incorrect Use-By-Dates. The mislabeled kits may no longer be safe or effective for their intended use.

    ModerateFDAJun 3, 2026Medtronic2 products

  • Devicor HydroMARK breast biopsy markers recalled for labeling mismatch

    Sold nationwide. Devicor Medical Products is recalling HydroMARK Breast Biopsy Site Marker Model 4010-02-15-T3 due to incorrect labeling on individual packages inside boxes. Some boxes labeled as T3 markers may contain packages labeled as T4 markers, which could lead to use of the wrong marker type during a breast biopsy procedure.

    ModerateFDAJun 3, 2026Devicor

  • Abiomed Impella Controller recalled for electrical and priming risks

    Sold nationwide. Certain Impella Controller (AIC) consoles contain electrical faults including alarm failures, power-path problems, and inaccurate motor sensing. Additionally, improper alignment between the purge cassette and motor drive can prevent the purge system from priming correctly, requiring users to switch to a backup console.

    SeriousFDAJun 3, 2026Abiomed

  • Medline spinal anesthesia kits recalled for bupivacaine quality issues

    Sold nationwide. Medline is recalling seven procedure kit products that contain bupivacaine hydrochloride in dextrose injection made by Huons Co. That bupivacaine was itself recalled over quality problems, including questions about microbiology testing data and reports of reduced effectiveness. No injuries have been reported.

    SeriousFDAJun 3, 2026Medline7 products

  • Halyard Purezero nitrile gloves recalled for chemical permeation failure

    Sold nationwide. Halyard Purezero Ultraviolet Nitrile Exam Gloves in sizes XS through XL failed to meet chemical permeation performance standards, meaning they may not provide adequate protection against certain chemicals. This affects approximately 452,500 units distributed nationwide.

    ModerateFDAJun 3, 2026Halyard

  • Abiomed Impella Controller recalled for potential safety concerns

    Sold nationwide. Abiomed identified that certain Automated Impella Controller (AIC) units have internal hardware issues that could affect device operation. These include cable and component positioning problems that may interrupt motor controls, cause startup failures, or prevent the device from booting properly. Abiomed is implementing hardware updates through its servicing process.

    SeriousFDAJun 3, 2026Abiomed

  • Bolton RelayPro stent-graft recalled for release risk

    Sold nationwide. The proximal clasp on Bolton Medical's RelayPro Thoracic Stent-Graft System may disconnect from the outer control tube during use. This disconnection could prevent the stent graft from being released properly from its delivery system. The FDA has issued a labeling update to inform physicians and hospitals of this potential issue.

    SeriousFDAJun 3, 2026Bolton Medical

  • Fly By Jing sesame noodles recalled for possible undeclared peanut

    Sold nationwide. Fly By Jing Creamy Sesame Noodles (3.8 oz packets) may contain peanuts due to cross-contamination during production, even though peanuts are not listed on the label. This poses a serious risk to people with peanut allergies. The recall affects approximately 3,419 cases with best-by dates between October 15, 2026 and March 23, 2027.

    ModerateFDAJun 3, 2026Fly By Jing

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