State
72,984 recalls have nationwide distribution and so reach Hawaii. 2,767 additional recalls listed Hawaii specifically in their distribution scope.
Of the 2,767 recalls naming Hawaii we have scored against our rubric, 333 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 567 (20%) are Severe.
Which agencies issued them
These figures cover only the 2,767 recalls whose distribution notice names Hawaii specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zero Motorcycles is recalling 2024 DSR/X, DS, DSR, and DSRP motorcycles because a twisted front brake hose may leak fluid and reduce braking ability.
Forest River is recalling 2026 Westbrook and Tracer recreational trailers because a liquid propane gas hose may rub against the furnace, causing a fuel leak that increases fire risk.
Jaguar is recalling certain 2021-2024 E-Pace vehicles because the passenger air bag may tear during deployment. 1,436 vehicles are affected.
Daimler Vans USA is recalling certain 2020-2023 Mercedes-Benz Metris vehicles because unsecured infotainment connections can stop the rearview camera image displaying. 43,422 vehicles affected.
Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an oversized spacer in the electric parking brake may cause overheating and fire.
Ozark Trail 64 oz Stainless Steel Insulated Water Bottles are being recalled because the lid can forcefully eject on opening. Three injuries are reported, including two cases of permanent vision loss.
SPPTTY kids 14- and 18-inch bicycles are being recalled because multiple components contain lead exceeding the federal lead content ban. About 200 units are affected.
WLIVE Fabric 15-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the federal standard under the STURDY Act. About 6,600 units affected.
Dearlomum retractable mesh safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor. About 2,200 units are affected.
Creekliybear "Pack and Play" aftermarket play yard mattresses are being recalled because they exceed thickness requirements and may not fit certain play yards. About 21,500 units affected.
Momentum Vida E+ e-bikes are being recalled because the fork steerer tube can crack, break or separate during use, posing a fall hazard. About 6,200 units are affected.
Unbranded braided crib bumpers are being recalled because they violate the federal crib bumper ban and can obstruct breathing. About 260 units are affected.
AUGNORYE padded cushioned crib bumpers are being recalled because they violate the federal crib bumper ban and can obstruct an infant's breathing. About 356 units are affected.
Tailstorm Health INC is recalling Lidocaine HCL Sterile Injection (20 mg/mL) due to FDA inspection findings of concerns with the sterile manufacturing process. The recalled product is distributed nationwide.
The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.
The Servo-u Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 874 units are affected.
The BiPAP A40 Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 6 units in the US and 67,534 outside it are affected.
Zicam Nasal AllClear swabs are being recalled because of fungal contamination of the nasal swabs. All lots are affected, covering 13,632 cartons.
Orajel Baby Cooling Swabs for Teething are being recalled because of fungal contamination of the infant oral swabs. All lots are affected, covering 695,880 cartons.
Buffered Penicillin G Potassium for Injection is being recalled because some vials of cefazolin for injection were incorrectly labeled as penicillin G potassium 20 million units.
Tailstorm Health Inc. is recalling bupivacaine HCL sterile injection vials nationwide due to FDA inspection findings regarding concerns with the sterile manufacturing process.
Sandoz Cefazolin for Injection 1 gram is being recalled after cartons were found to contain vials labeled as penicillin G potassium. 208,300 vials are affected.
Philips Ultrasound, Inc is recalling 5,230 Philips 3D9-3v Transducer devices because they were refurbished beyond their useful life, posing a risk of device failure during medical use.
The Servo-n Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 7,688 units affected.
Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.