State
73,388 recalls have nationwide distribution and so reach Alaska. 1,765 additional recalls listed Alaska specifically in their distribution scope.
Of the 1,765 recalls naming Alaska we have scored against our rubric, 118 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 470 (27%) are Severe.
Which agencies issued them
These figures cover only the 1,765 recalls whose distribution notice names Alaska specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The FDA is recalling the VELYS Robotic-Assisted Solution Base due to a software defect in version 1.5.1 related to Daylight Saving Time changes. The defect can cause system errors requiring restart, potentially delaying patient treatment.
Siemens Healthcare is recalling all lots of the ADVIA Centaur Enhanced Estradiol diagnostic test because plasma specimens can produce falsely elevated results, potentially leading clinicians to misinterpret patient results.
Siemens Atellica IM Enhanced Estradiol test kits can produce falsely elevated results in plasma specimens, potentially leading to misinterpretation of patient hormone measurements. Approximately 2,044 units worldwide are affected.
An estradiol diagnostic device has been recalled because it produces falsely elevated test results in plasma specimens. These inaccurate results could cause clinicians to misinterpret patient test results.
Macleods Pharma is recalling Losartan Potassium Tablets due to CGMP deviations with azido impurity levels exceeding acceptable limits. The recall affects 5.6 million tablets distributed nationwide.
SCA Pharmaceuticals has recalled Vancomycin HCl 1.5g injection bags due to manufacturing process deviations. The product was distributed nationwide.
McKesson Corporation is recalling Erythromycin Topical Gel USP 2% due to CGMP deviations. The manufacturer discontinued its stability study program, prompting a nationwide recall of all products within their expiration date.
Akorn, Inc. is recalling 66,744 bottles of Lidocaine Hydrochloride Oral Topical Solution, USP 2% (Lot #370978) nationwide because the product's viscosity was below the required specification.
restor3d Inc. is recalling 14 units of its Non-Sterile Double Ended Trial Kit because the product was labeled as Small Footprint when it is actually Medium. The lot was distributed nationwide across seven states.
SCA Pharmaceuticals recalled 120 bags of Norepinephrine 8mg injection nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall was initiated April 25, 2022.
Lupin Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg tablets nationwide due to AZIDO impurity levels above acceptable limits. Patients should consult their healthcare provider about their medication.
Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to AZIDO impurity levels exceeding acceptable manufacturing standards. The prescription blood pressure medication was distributed nationwide.
SCA Pharmaceuticals voluntarily recalled 424 bags of fentanyl and bupivacaine injectable solution due to manufacturing control deviations. The product was distributed nationwide in the United States.
Jaguar Land Rover is recalling 2022 New Range Rovers because improperly tightened fasteners may cause front crash sensors to malfunction, affecting air bag deployment.
Braxton Creek RV is recalling 2022 Free Solo, Bushwhacker, and Bushwhacker Plus travel trailers because cracked LP gas fittings may cause a leak and fire.
Certain 2022 Rivian R1T vehicles have a malfunctioning occupant classification system that fails to deactivate the front passenger airbag when a child or child seat is present, increasing injury risk during a crash.
Winnebago is recalling 2021-2023 Ekko recreational vehicles because quick disconnect fittings in the LP gas system may crack, potentially causing a gas leak that could lead to fire.
Custom Fire is recalling 2021-2022 Spartan emergency vehicles because a rear axle part may fracture, potentially causing the parking brake to engage unexpectedly and increasing crash risk.
Mercedes-Benz is recalling 2006-2012 ML, GL, and R-Class vehicles because moisture in the brake booster can cause corrosion, leading to reduced brake performance or failure.
Mercedes-Benz is recalling 2021 GLB 250 vehicles because a rear axle sensor linkage may be improperly installed, potentially causing headlight glare that increases crash risk.
Tesla recalls 2020-2021 Model 3 and 2021 Model Y vehicles due to incorrectly installed camera cable terminals that cause swapped camera views, impairing collision detection and automatic emergency braking.
Sumitomo is recalling certain Sumitomo and Falken tires because a deformation near the bead could cause separation, increasing the risk of a crash.
Cruiser RV is recalling 2022 Shadow Cruiser trailers because a missing breaker cover exposes studs, creating a risk of electrical arcing, fire, and injury.
Hyundai is recalling 2021-2022 Accent vehicles because a steering column bolt may not be properly secured. This can cause the steering column to detach, resulting in loss of steering control and increased crash risk.
Continental Tire is recalling specific motorcycle tires because cracks in the tread grooves can lead to tread separation, increasing the risk of a crash.