State
20,322 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho 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 Idaho 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.
Jetson Electric Bikes is recalling about 53,000 Jetson Rogue 42-volt self-balancing scooters due to overheating lithium-ion batteries that pose a fire hazard. Two deaths have been reported.
Lithium-ion battery packs in Higdon Outdoors XS Series waterfowl decoys can overheat and catch fire while charging. The manufacturer received 20 overheating reports including 9 fires, 7 with property damage, though no injuries have been reported.
JBM International is recalling about 5,300 adult bike helmets sold on Amazon.com from March 2022 through January 2023 because they do not meet federal safety standards and can fail to protect the head in a crash.
Solexio STYLR Hair Stylers are being recalled because the power cord can detach if the unit is dropped, creating an electrocution or shock hazard. Consumers should stop using the product immediately and contact the company for a refund.
Cannondale is recalling about 75 Tesoro Neo X Speed electric bicycles because the hand brakes are configured to the European standard, which is reversed from the U.S. standard, creating a fall and injury hazard to riders.
Polaris is recalling about 200 Model Years 2022-2023 RZR Pro R and Pro R 4 recreational off-road vehicles because the alternator can fail during operation and pose a fire hazard. The company has received four reports of alternator failure, including two fire incidents, with no injuries reported.
Delta Enterprise Corp. is recalling approximately 43,380 2-in-1 Outdoor Kids Swings because the seat restraint straps can break, creating a fall hazard for young children. No injuries have been reported.
Carhartt Men's Force Relaxed 5 Pocket Work Pants can develop an extended elastic loop at the ankle that poses a trip and fall hazard. About 32,505 units sold at Dick's Sporting Goods from July through November 2022 are affected.
Open Cycle UP Ekar, UPPER Ekar, WIDE Ekar, and MIND Ekar bicycles with Campagnolo hydraulic rear disc brakes are being recalled because the rear brake can fail, posing a crash hazard. About 270 units sold nationwide from November 2021 through February 2023 are affected.
Delsam Pharma's Artificial Eye Ointment is being recalled for bacterial contamination in unopened tubes. FDA analysis found non-sterility defects in approximately 50,000 units.
DePuy Orthopaedics is recalling Attune Posterior tibial insert implants that received excessive gamma radiation during manufacturing, which may degrade the material properties of the knee replacement component.
DePuy Orthopaedics is recalling 7 units of the Attune Revision Limb Preservation System Tibial Insert (Lot JP9022) that received higher than specified gamma radiation doses. The over-irradiation may cause changes to implant material properties.
DePuy Orthopaedics is recalling Attune Revision LPS Tibial Insert devices (Lot JP9016) because they received excessive gamma radiation during manufacturing, which may compromise material properties.
Raystation radiation therapy planning software may not correctly export collimator angle settings when using the DICOM export function. In exported files, the collimator angle may be replaced with zero regardless of the user's selection.
Boehringer Ingelheim Pharmaceuticals is recalling Jardiance (Empagliflozin) 25 mg tablets due to a label mix-up affecting 69,375 bottles distributed nationwide.
DePuy Orthopaedics recalls 7 units of Attune Revision LPS Tibial Inserts (Part 151760118, Lot JP6452) distributed worldwide due to excessive gamma radiation during manufacturing. This overage may result in material property changes.
CareFusion recalls 7,914 units of BD Pyxis automated medication dispensing systems after firmware was inadvertently downgraded during installation, potentially causing drawer failures and medication delivery delays.
Vapotherm has recalled 5,869 Low Flow Disposable Patient Circuits for the Precision Flow System due to reports of excessive condensation that may lead to rainout.
DePuy Orthopaedics is recalling 7 units of the Attune Revision Tibial Insert that received excess gamma radiation during manufacturing, which may degrade implant material properties.
Noven Pharmaceuticals is recalling specific lots of Daytrana (methylphenidate) transdermal patches due to a defective delivery system that is out of specification for shear. Affected lots are Lot 91956 (6/2023) and Lot 92475 (7/2023), distributed nationwide.
Noven Pharmaceuticals recalls Daytrana (methylphenidate) 30 mg transdermal patches nationwide due to defective delivery system components that fail shear specifications. Patients should contact their healthcare provider regarding medication alternatives.
Withings Scan Monitor/ScanWatch (model hwa09) has a software defect preventing physicians from reviewing ECG recordings, which is critical to the device's FDA clearance requirement for physician-supervised use. Users should discontinue use until the defect is corrected.
Noven Pharmaceuticals is recalling Daytrana methylphenidate transdermal patches for a defective delivery system that fails to meet shear specifications. The recall affects specific lots distributed nationwide.
Noven Pharmaceuticals is recalling specific lots of Daytrana methylphenidate transdermal patches distributed nationwide because the delivery system is out of specification for shear. The affected lots require patient and healthcare provider attention.
CooperVision is recalling Clariti 1-day toric contact lenses from lot W0124677 because they were made with a misaligned axis that results in incorrect lens power.