State
72,913 recalls have nationwide distribution and so reach Hawaii. 2,766 additional recalls listed Hawaii specifically in their distribution scope.
Of the 2,766 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 2,766 recalls whose distribution notice names Hawaii specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Stryker Sustainability Solutions is recalling Daig Livewire Steerable BDB reprocessed electrophysiology catheters due to incomplete seals on the sterile product.
Stryker Sustainability Solutions is recalling BARD Dynamic Tip Steerable reprocessed electrophysiology catheters (Product Number 200131) due to incomplete seals on sterile product packaging. The recall affects 61 units distributed nationwide in the US and in Israel and Canada.
Stryker Sustainability Solutions is recalling 458 units of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging.
Stryker Sustainability Solutions is recalling BARD Dynamic XT Steerable reprocessed electrophysiology catheters (Product Number 201103) due to incomplete seals on the sterile product packaging.
Volkswagen is recalling certain 2024 Tiguan vehicles previously repaired under recall 25V082 because a camera control unit error at startup can stop the rearview image displaying.
Stryker Sustainability Solutions is recalling three lots of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile packaging. The defect affects units distributed in the US, Israel, and Canada.
Stryker Sustainability Solutions is recalling BARD Dynamic Deca Steerable reprocessed electrophysiology catheters (Product Number 201101) distributed nationwide and in Israel and Canada due to incomplete seals on the sterile product packaging. The incomplete seals may compromise sterility.
Alliance RV is recalling certain 2022-2025 Valor and Paradigm recreational trailers because the heating pad may not be appropriate for lithium battery applications.
Blue Bird is recalling 2027 Vision school buses because wheelchair retractors may fail to lock. This defect could allow wheelchairs to move during transit, increasing injury risk.
The CS Uni-Directional with Auto ID reprocessed electrophysiology catheter is being recalled because of incomplete seals on the sterile product. 449 units are affected.
The Dakota Honey Company Honey Flight, a four-flavour spun honey set, is being recalled because of a foreign object: stainless steel dust or flakes, or shreds of plastic.
Stryker Sustainability Solutions is recalling Daig Livewire Steerable electrophysiology catheters with incomplete seals on sterile packaging. The defect may allow contamination of the sterile product.
Wabash is recalling 2019-2027 Transcraft and Wabash Platform trailers because missing conspicuity tape reduces visibility, increasing crash risk.
Dakota Honey Company Spreadable Spun Honey in salted caramel flavour is being recalled because of a foreign object: stainless steel dust or flakes, or shreds of plastic.
Lippert is recalling Curt Touring Coil Suspensions because shock bolts may be incorrectly tightened, creating a road hazard.
Stryker Sustainability Solutions is recalling 154 units of BW Webster Duo-Decapolar reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging, which may compromise sterility.
Dakota Honey Company Spreadable Spun Honey in jalapeno flavour is being recalled because of a foreign object: stainless steel dust or flakes, or shreds of plastic.
Stryker Sustainability Solutions is recalling BARD Dynamic Tip Steerable reprocessed electrophysiology catheters (Product Number 200344) due to incomplete seals on sterile product packaging that could compromise sterility.
Dakota Honey Company Spreadable Spun Honey in original flavour is being recalled because of a foreign object: stainless steel dust or flakes, or shreds of plastic.
Turtle Top is recalling 2026 Terra Transit and Odyssey buses because wheelchair retractors may fail to lock, increasing injury risk.
KZRV is recalling 2026 Durango recreational trailers because shock bolts may be incorrectly tightened, creating a road hazard risk.
Dakota Honey Company Spreadable Spun Honey in cinnamon-infused flavour is being recalled because of a foreign object: stainless steel dust or flakes, or shreds of plastic.
Dexcom, Inc. is recalling Dexcom ONE+ iOS CGM App versions 1.5.0 and 1.6.0 due to a software defect that can delay glucose alerts and notifications, risking delayed detection of low or high blood sugar events.
Diowave 250W Laser Systems require a software update because some units operate at up to 70W maximum average power output, exceeding the FDA-cleared limit of 60W.
Integra LifeSciences is recalling Codman CerebroFlo EVD Catheters (Lot 45322) because endotoxin levels did not meet acceptance criteria. The product was distributed nationwide.