State
73,092 recalls have nationwide distribution and so reach Hawaii. 2,770 additional recalls listed Hawaii specifically in their distribution scope.
Of the 2,770 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 569 (21%) are Severe.
Which agencies issued them
These figures cover only the 2,770 recalls whose distribution notice names Hawaii specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boston Scientific is recalling HOT AXIOS Stent systems due to potential outer sheath detachment that can prevent proper stent expansion. This defect may require device replacement during the procedure.
Medline SHORT TERM INFUSAPORT ACCESS KIT with reorder number DYNDC3188 is recalled because included surgical masks failed bioburden testing, potentially compromising sterility during procedures.
McKesson is recalling Inflectra (infliximab-dyyb) injectable drug due to manufacturing quality deviations. A batch intended for quarantine was inadvertently distributed to patients nationwide.
Boston Scientific's AXIOS Stent Delivery System (47 units affected) is recalled because the outer sheath can detach and prevent proper stent expansion, requiring device exchange.
Boston Scientific's HOT AXIOS stent delivery system may have an outer sheath that detaches and prevents proper stent expansion. The defective tip can remain around the stent, requiring device exchange during the procedure.
Boston Scientific recalls 1,399 units of AXIOS stent delivery systems due to outer sheath detachment that can prevent proper device expansion, requiring procedure prolongation and device exchange.
LivaNova's SenTiva DUO vagus nerve stimulation device may stop delivering therapy due to an internal component issue. The recall affects 84 units distributed worldwide.
Boston Scientific is recalling HOT AXIOS Stent systems because the outer sheath's tip can detach and prevent proper stent expansion, requiring device replacement during procedures.
Snap rings may detach from internal shafts in CyberKnife Treatment Delivery Systems, potentially causing uncontrolled rotation on treatment axes. This affects 212 units distributed worldwide for stereotactic radiosurgery.
Karl Storz Endoscopy is recalling 59 units of its uretero-renoscope due to instructions for use containing reprocessing procedures that the FDA has not reviewed or approved for safety and efficacy.
Boston Scientific is recalling AXIOS Stent devices due to outer sheath distal tip detachment that can prevent proper stent expansion and require device replacement during the procedure.
Karl Storz is recalling 180 ureteroscopes due to instructions for use containing reprocessing procedures that have not been reviewed or approved by the FDA.
Boston Scientific's AXIOS Stent Delivery System is being recalled because the outer sheath can detach during use, preventing proper stent expansion and requiring device exchange.
The W.S. Badger Company is recalling Badger 50 mineral sunscreen tins lacking the complete drug facts label, barcode, and directions for use. The recall affects 4,834 tins distributed nationwide.
Medline procedure kits containing surgical masks are recalled nationwide because included masks failed to meet bioburden testing standards, creating potential infection risk during medical procedures.
Highland Ridge RV is recalling 2025 Open Range 3X fifth-wheel travel trailers because the vehicle certification label lists the wrong tire size, which could lead to incorrect tire installation.
Temsa is recalling 2024 TS35 vehicles with Cummins L9 engines because fuel filter hoses may separate, causing leaks, engine stalls, and fire or crash risks.
New Flyer is recalling 210 transit buses because fuel filter hoses may separate, causing leaks, engine stalls, and fire risks.
Ford is recalling 2025 Bronco Sport, Escape, and Lincoln Corsair vehicles because the instrument panel may fail to illuminate, increasing crash risk.
Ford is recalling certain 2021 Expedition, 2021-2022 Super Duty F-250 to F-600 and 2020-2022 Lincoln Corsair vehicles because the rearview camera may display a blank or distorted image.
Roadtrek is recalling 2023-2025 Westfalia Wave Pop Top vans because incorrect weight labels may lead to unintentional overloading and increased crash risk.
AMX Global is recalling about 22,500 portable folding stadium seats because security hooks can crack and break, posing fall and injury risks. The company received reports of hook failures including falls and an injury.
Autocar is recalling 2023-2025 E-ACTT vehicles because a software error may cause the vehicle to roll away on an incline or stall the engine.
AliExpress is recalling about 980 Multi Styler Hair Dryers sold online from May 2023 through November 2024 because they lack an immersion protection device and pose an electrocution hazard if they fall into water while plugged in.
Pearhead Infant Learning Toy Sets are recalled because the wooden egg-shaped rattle can lodge in a child's throat, creating a choking hazard. The recall affects about 2,700 units sold from August through October 2024.