State
73,100 recalls have nationwide distribution and so reach Idaho. 3,520 additional recalls listed Idaho specifically in their distribution scope.
Of the 3,520 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,025 (29%) are Severe.
Which agencies issued them
These figures cover only the 3,520 recalls whose distribution notice names Idaho specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jayco is recalling 2024 North Point and Pinnacle travel trailers because a faulty air conditioner component may overheat and cause a fire.
Quad Lock is recalling about 13,700 MAG Battery Packs in the US due to fire hazard. The battery can overheat; the company received reports of fires and property damage.
Baofali 4-in-1 Microfiber Crib Safety Bumpers sold on Temu.com violate the federal crib bumper ban and pose a suffocation hazard to infants. About 390 units were sold from June through August 2024.
Hyundai is recalling 34,964 units of the 2024 Santa Fe and Santa Fe Hybrid with faulty switch knobs that may not retract, creating an injury risk.
Wolf Appliance is recalling about 44,000 Dual Fuel ranges with infrared griddles due to a short-circuit hazard. Liquid spillage can unexpectedly activate the griddle, posing burn and fire risks. No injuries have been reported.
Kyte Baby is recalling about 20,500 Slumber Suits sold from November 2022 to March 2024 because they violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. No injuries have been reported.
Dreamgro Lullaby mermaid travel soothers are recalled because a gold-colored soft star can detach, posing a choking hazard to infants. No injuries have been reported, but one detachment incident was confirmed.
GM is recalling 2022-2023 Chevrolet Express and GMC Savana vehicles for a transmission software defect that may cause rear wheel lockup and unintended vehicle movement. Dealers will update the software free of charge.
Micro Bird is recalling 2023 CT-Series buses because the ignition interlock may allow the vehicle to start with the rear emergency door locked, increasing injury risk.
Nikola is recalling 2022-2023 Tre BEV vehicles because a resistor may degrade, causing the instrument panel to fail and potentially hide critical safety information.
Micro Bird is recalling 2022-2024 T-Series school buses because the ignition interlock may allow the vehicle to start with the rear emergency door locked, increasing injury risk.
Guava Roam strollers are recalled because the brakes can fail to engage or unexpectedly disengage, posing fall and injury hazards to children. No injuries have been reported.
PJ TRAILERS is recalling certain 2024-2025 LD trailers because air ride suspension brake axles may be installed incorrectly. This could reduce braking ability and increase the risk of crashes.
Percussionaire Corporation is recalling Phasitron5 breathing circuits (P5-10, P5-HC, P5-UC-10) due to discolored fluid caused by an unintended nickel coating on the spring component reacting with medicated mist. 43,830 devices have been distributed across the U.S.
Maquet Cardiovascular is recalling the VasoView HemoPro Endoscopic Vessel Harvesting System due to silicone detachment from the Harvesting Tool Jaws during use. This FDA Class I recall affects 28,809 units worldwide.
Olympus Corporation recalls 279 units of its ESG-410 electrosurgical generator nationwide due to increased complaints of system error E1226 (Could not write to Audio Buffer) occurring during surgical procedures.
Integra LifeSciences recalls 1,222 Surgical Patties and Strips (Model 801455) due to elevated endotoxin in raw material, which may contaminate finished products used to protect tissue during surgery.
Covidien is recalling specific lots of its Chameleon PTA Balloon Catheter that failed in-house pressure testing. The affected catheters were distributed worldwide to the US and 18 countries.
Integra LifeSciences Corp. is recalling surgical patties and strips due to higher-than-expected endotoxin levels in raw material that may have resulted in out-of-specification finished products used during surgery.
Olympus is recalling the OFP-2 Endoscopic Flushing Pump due to intermittent loss of function caused by internal component connection failure. Approximately 445 units distributed nationwide are affected.
Dr. Reddy's Laboratories recalls Cinacalcet 30 mg tablets nationwide due to manufacturing defects that produced N-nitroso impurity above FDA recommended limits. Patients should contact their healthcare provider if they are taking an affected lot.
Integra LifeSciences Corp. is recalling surgical patties and strips (Model 801402) used in surgery due to higher-than-expected endotoxin levels in raw materials that may affect the finished product.
Integra LifeSciences is recalling Surgical Patties and Strips (Model 801457) due to higher-than-expected endotoxin levels in raw materials. These surgical devices protect tissue during operations, including brain and nervous system procedures.
Accord Healthcare recalls Cinacalcet 60mg tablets nationwide because N-nitroso-cinacalcet impurity was detected above acceptable daily intake limits. The contamination resulted from manufacturing process deviations.
Integra LifeSciences is recalling surgical patties and strips (Model 801452) due to higher-than-expected endotoxin levels in raw materials that may result in out-of-specification contamination. Approximately 4,818 units are affected.