State
73,827 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.
Of the 4,916 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,351 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Peg Perego is recalling about 3,000 850 Polaris Sportsman ride-on vehicles because a circuit board defect can cause overheating, fire, and burns.
Forest River is recalling 2017 Vibe trailers because the kitchen stove may be connected to a live electrical circuit, posing a shock hazard.
Jayco is recalling 2017 Jay Sport camping trailers because tire labels list the wrong tire size and pressure, which could lead to over-inflation and tire failure.
Ford is recalling 2015-2017 Mustangs because an engine oil cooler hose may separate, causing an oil leak that could lead to engine failure or fire.
Synergetics Inc is recalling 72 units of 25 gauge VersaVit 2.0 Core Essentials Procedure Packs because the vitrectomy cutters do not operate within correct pressure pulse specifications.
Dollar General is recalling Soft Baked Chocolate Brownie Cookies due to the presence of mold. Consumers should discard the product or return it for a refund.
Windstone Medical Packaging is recalling 852 Major General Packs because Medtronic gloves inside may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 115 Peri Kits (PSS1037) because the included Medtronic gloves may contain splits or holes that compromise sterility.
Vascular Solutions is recalling Twin-Pass RX Dual Access Catheters because excess manufacturing material may remain at the tip or within the distal lumen.
Forest River is recalling 2016 Rockport cargo and work trucks because the rear ramp may damage fuel connections, causing engine stalls and crash risk.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility in custom surgical kits.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because they may contain splits or holes that compromise sterility.
Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the tip or in the distal lumen.
Ford is recalling specific 2010-2012 Escape and 2010-2011 Mariner vehicles because a cracked fuel delivery module may cause a fuel leak, increasing the risk of fire.
Del Monte is recalling cut green beans and field peas with snaps due to a customer complaint of finding crawfish parts in the product.
Heartware, Inc. is recalling Ventricular Assist System Controllers due to loose connector ports. The recall affects 4,235 units worldwide, including 7,272 in the U.S.
Del Monte is recalling approximately 15,000 cases of canned field peas and green beans after a customer complaint reported finding crawfish parts in the product.
Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the catheter tip or within the distal rapid exchange lumen.
Ford is recalling 2017 F-250 through F-550 Super Duty trucks because a fuel shield may detach, causing a leak that increases fire risk.
Teleflex Medical is recalling Willy Rusch Tracheostomy Tube Sets because the connector may disconnect from the tube during use.
Windstone Medical Packaging is recalling 304 Endoscopy Packs because disposable gloves in the kits may have splits or holes that compromise sterility.
RTI Surgical is voluntarily recalling 66 units of Streamline OCT spinal rods due to potential cracks that could reduce strength and cause patient injury.
Awareness Corporation is recalling 2,697 bottles of Boost Tea dietary supplement due to potential Salmonella contamination. The product was distributed in 34 U.S. states and D.C.
Windstone Medical Packaging is recalling 816 Extremity Tray kits because the included Medtronic gloves may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 12 Major Laparotomy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.