State
73,588 recalls have nationwide distribution and so reach Alaska. 1,766 additional recalls listed Alaska specifically in their distribution scope.
Of the 1,766 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 1,766 recalls whose distribution notice names Alaska specifically. The 73,588 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hyundai is recalling 2007-2012 Veracruz vehicles because an oil leak can damage the alternator, causing the charging system to fail and potentially leading to an engine stall.
Certain 2021 Winnebago motorhomes are being recalled because the power bed motor may fail internally, causing the bed to extend before the safety strap engages. This can result in the bed falling unexpectedly, posing a risk of injury or death.
InvoSpa is recalling electric throw heated blankets sold on Amazon.com because they can overheat, posing fire and burn hazards.
Chrysler is recalling 2014-2019 Jeep Grand Cherokee vehicles with 3.0L EcoDiesel engines because a cracked EGR cooler may cause an intake manifold fire.
Lion Electric is recalling 2016-2019 Lion C and 360 school buses with wheelchair lifts because shoulder belt and ground anchors may detach in a crash.
BMW and Toyota are recalling certain 2020-2021 Z4 and Supra vehicles due to insufficient fuel tank welds that may cause fuel leaks and increase fire risk. Owners should contact their dealer for a free replacement.
Certain 2021 Toyota RAV4 Prime vehicles have improperly closed headlight aiming caps that can be adjusted horizontally. This can increase glare and reduce driver visibility, increasing the risk of a crash.
Zinus is recalling about 26,000 metal bunk beds because welds on the upper bunk can fail, causing the bed to collapse and posing fall and injury hazards.
Zimmer Biomet is recalling 412 acetabular hip prosthesis cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 acetabular hip cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 acetabular hip cup components because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Nostrum Laboratories is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg because the NDMA impurity level exceeds acceptable intake limits.
Nostrum Laboratories is recalling 20,872 bottles of Metformin Hydrochloride Extended-Release Tablets 500 mg because they contain N-Nitrosodimethylamine (NDMA) above acceptable levels.
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
PD-Rx Pharmaceuticals is recalling 125 bottles of Metformin Hydrochloride Extended Release tablets because of NDMA impurity levels above acceptable limits.
Marksans Pharma Limited is recalling Metformin Hydrochloride Extended Release tablets due to N-Nitrosodimethylamine (NDMA) impurity levels above acceptable intake limits.
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
PD-Rx Pharmaceuticals is recalling 1,683 bottles of Metformin Hydrochloride Extended Release 500 mg because of NDMA impurity levels above acceptable limits.
Terex is recalling 2019-2020 TL80 and TL100 aerial devices because rotation bearing bolts may loosen and fail, potentially causing the boom to fall.
Denton Pharma, Inc. is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg due to the detection of N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels.
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.