State
20,096 recalls have nationwide distribution and so reach Utah. 0 additional recalls listed Utah specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Utah consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Ford is recalling certain 2023 Super Duty F-250, F-350, F-450, F-550 and Escape models. The instrument panel module may fail to illuminate due to improper soldering, preventing drivers from seeing critical safety information like the speedometer and warning lights.
Prevost recalls certain 2005-2024 buses with wheelchair lifts due to a potentially steep bridging device that can cause wheelchair instability. Affected owners should contact Prevost for a free replacement.
Volkswagen is recalling certain 2023 GTI and Golf R vehicles due to deformed suspension strut mounts that may loosen and cause steering instability. Dealers will replace affected components at no cost.
Volkswagen is recalling 2022 ID.4 vehicles with defective rearview camera software. The defect can delay or deactivate the rearview camera image, reducing rear visibility and increasing crash risk.
Airstream is recalling certain 2023 Bambi travel trailers due to an overstated freshwater tank capacity that resulted in an incorrect cargo carrying capacity label. The mislabel could lead to unintentional overloading and increased crash risk.
Oliver is recalling 1,304 LEGACY ELITE II trailers (2009-2024) due to an underrated towing coupler that may break, creating a risk of trailer detachment and crash.
Delta Cycle Corp is recalling ceiling hoists with straps because plastic buckles can break when holding kayaks, canoes, or other large objects. The company has received four incident reports, including one minor injury.
Rivian is recalling 2024 R1S and R1T vehicles with missing dashboard airbag warning labels. The missing label may prevent drivers from understanding airbag safety risks to children in the front seat.
Honda is recalling 2020–2024 Ridgeline vehicles because the rearview camera wire harness may fatigue and break, preventing the camera image from displaying and reducing rear visibility.
GM is recalling 2024 Cadillac Lyriq and related vehicles due to faulty rear drive wiring that can cause loss of power and increase crash risk.
Thor Motor Coach is recalling approximately 2,919 motorhomes with fuel hose clamps that may lack adequate clamping force, risking gasoline leaks and fires. Owners should contact dealers for free fuel hose and clamp replacement.
BVI CustomEyes Procedure Packs containing Sol-M manufactured low dead space and Luer Slip syringes are subject to a voluntary recall. Approximately 142 units were distributed nationwide.
Five Afinion 2 lab analyzers were distributed with incorrect configuration, potentially allowing waived laboratories to perform moderately complex assays that could produce erroneous results.
Beaver Visitec International voluntarily recalls BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The recall affects 351 units distributed nationwide.
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing Sol-M-manufactured syringes. The recall affects 138 units distributed nationwide.
Stryker Corporation is recalling the iBur 3.0mm Precision Match Head surgical burr because it may generate higher-than-specified temperatures during use, potentially causing thermal injury that may require medical intervention.
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs because they contain Sol-Millennium Medical syringes that are subject to a manufacturer recall. A total of 103 units were distributed nationwide.
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing Sol-M syringes distributed nationwide. The recall affects 35 units with Part Number 584770 and is classified as FDA Class II.
Stryker recalls iBur 3.0mm Precision Round surgical burs due to potential for excessive temperatures where the bur shank meets the bushing. Thermal injury risk may require medical intervention.
Stryker recalled 1,226 iBur surgical burrs with multiple lot numbers worldwide due to potential overheating at the bur-shank connection point, which could cause tissue damage requiring medical intervention.
OrthoPediatrics Canada is recalling FRT250 cartridges used in the Fassier-Duval Telescopic IM System because an incorrect component was substituted during assembly.
Stryker Corporation recalls iBur 3.0mm surgical burs used in neurosurgery, spinal, and ENT procedures due to potential overheating at the bur-shank interface. The heat risk may cause tissue damage requiring medical intervention.
Dr. Reddy's Laboratories is recalling 31,802 bottles of IBU Ibuprofen 600mg tablets due to failed impurity specifications. The product was distributed nationwide and in Puerto Rico.
NOW Real Foods Whole & Unsalted Raw Brazil Nuts are recalled due to high levels of mold, yeast, and microbial contamination. The recall affects 7,854 units distributed nationwide and to Singapore.
Agfa is recalling 141 DR 800 Digital Radiography X-ray systems for potential failure of the table's front lever chain.