State
73,737 recalls have nationwide distribution and so reach New Mexico. 3,636 additional recalls listed New Mexico specifically in their distribution scope.
Of the 3,636 recalls naming New Mexico we have scored against our rubric, 745 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 815 (22%) are Severe.
Which agencies issued them
These figures cover only the 3,636 recalls whose distribution notice names New Mexico specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Polaris is recalling 2018-2020 Phoenix 200 ATVs because a damaged throttle lever stop can cause a crash. No injuries have been reported.
Certain 2017-2021 Freightliner Cascadia tractor trailers are recalled due to chemical corrosion in the brake modulator valve, which can slow brake release and cause brakes to pull to one side during automatic braking, increasing crash risk.
Kia is recalling 2015-2016 Soul EVs because the parking mechanism may be damaged if the driver shifts to Park before the vehicle stops, potentially causing unintended movement.
A Better You! is recalling Belecoo 535-S baby strollers because they violate federal safety standards, posing entrapment, strangulation, and fall risks to children.
Edens Garden is recalling Wintergreen and Birch Essential Oils because the bottles lack child-resistant caps, posing a poisoning risk to young children.
Jayco is recalling 2017 North Point fifth wheel trailers because leaf springs may fail to support loads, risking tire damage and loss of control.
Polaris is recalling approximately 26,730 Ranger and General utility vehicles because a software defect may cause sudden acceleration after a restart, posing a crash risk.
Avalon Furniture is recalling Cottage Town Bedroom Furniture sold at Rooms To Go because the base coat paint contains lead levels exceeding federal standards, posing a poisoning risk.
Amneal Pharmaceuticals is recalling 192 bottles of Metformin Hydrochloride Extended-Release Tablets, 500 mg, due to N-Nitrosodimethylamine (NDMA) impurity levels above acceptable intake limits.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Amneal Pharmaceuticals is recalling specific lots of Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected NDMA impurity above acceptable intake levels.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected NDMA impurity above acceptable intake levels.
BIOTA Biosciences is recalling Sterile Curcumin 50mg/mL vials due to lack of assurance of sterility and the presence of unapproved ingredients.
BIOTA Biosciences is recalling sterile Cannabidiol and Curcumin vials due to lack of sterility assurance and lack of FDA approval.
Forest River is recalling 2016 Amera-Lite Cargo Van trailers because insufficient drawbar steel thickness may cause fractures, leading to loss of control or detachment.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) above acceptable intake levels.
NOW Health Group is recalling 4,251 bags of Raw Macadamia Nuts because the product tested positive for Salmonella enterica.
Hino is recalling 2021 NJ8A heavy trucks because incorrect software may cause the anti-lock braking system to deactivate, increasing crash risk.
Time-Cap Labs is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis found NDMA impurity above acceptable levels.
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Biota Biosciences is recalling sterile cannabidiol vials because they may not be sterile and were marketed without FDA approval.
BIOTA Biosciences is recalling sterile curcumin vials because the product lacks assurance of sterility and contains unapproved ingredients.