State
72,907 recalls have nationwide distribution and so reach Idaho. 3,517 additional recalls listed Idaho specifically in their distribution scope.
Of the 3,517 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 1,023 (29%) are Severe.
Which agencies issued them
These figures cover only the 3,517 recalls whose distribution notice names Idaho specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Diamond Coach is recalling 2025-2026 VIP motorcoaches because wheelchair retractors may fail to lock, increasing injury risk during transit.
About 13,400 sets of Honlyne LED party favors are being recalled because the battery compartments contain button cell batteries that can be easily accessed by children.
About 20 Treatlife Smoke and Carbon Monoxide Detectors are being recalled because they can fail to alert consumers of a fire.
About 14,700 Lomi Roll-On Waxing Kits are being recalled because the warmer's power cord can overheat and short circuit, posing fire, burn and shock hazards.
About 200 XW-A17 Electric Youth ATVs are being recalled because they are missing brake lights, violating the mandatory safety standard for ATVs.
About 7,400 Super Off-Road 12,000 mAh Solar Wireless Power Banks are being recalled because the lithium-ion battery can swell and overheat, posing a burn hazard.
About 500 pairs of Raychy Children's Light Sneakers are being recalled because the lithium coin batteries can be accessed easily by children, posing an ingestion hazard.
About 8,420 bottles of MedPride Baby Oil are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
About 13,514 Amana window and through-the-wall air conditioners and heat pumps are being recalled because the heating element can remain energized during a ground fault.
About 1,013 Small Fish Montessori Busy Board toys are being recalled because magnets can detach, posing an ingestion hazard.
About 130 Kith-branded children's plaid loungewear sets are being recalled for violating the mandatory flammability standards for children's sleepwear.
USDA FSIS issued a public health alert for PRIVATE SELECTION Honey Dijon Boneless Skinless Chicken Breasts due to misbranding and undeclared eggs. The product label contained the wrong ingredients statement and failed to declare the egg allergen present in the product.
Arrow SAC catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall.
Arrow AHDC three-lumen catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 4,270 units affected.
Arrow two-lumen hemodialysis kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 15,425 units affected.
Arrow central venous catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 308,263 units affected.
Arrow spinal anesthesia kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 79,614 units are affected.
Arrow access trays and StimuCath safety kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 205,685 units affected.
The Arrow peritoneal lavage catheter kit, 8 Fr, is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 7,560 units affected.
Automated Impella Controllers are being recalled because of a potential software error when used with left ventricular Impella devices. 10,297 units are affected.
The Arrow Access Tray, REF ASK-04001-MC3, is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 8,265 units affected.
Arrow arterial line, radial artery and vessel catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall.
Arrow access trays and multilumen PI CVC kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 1,061,069 units affected.
The Arrow PICC Access Tray, REF ASK-04001-CG1, is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 360 units affected.
The Arrow two-lumen 12 Fr x 16 cm hemodialysis kit is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 1,945 units affected.