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.
The Protein Shoppe is recalling Red-E Tablets found to contain sildenafil, an unapproved drug for erectile dysfunction. The product was marketed without FDA approval.
Frito-Lay is recalling 10-count Lays sacks in 11 states due to a potential undeclared milk allergen.
Ford is recalling 2020 F-350 trucks with ambulance prep packages because incorrect rear axles were installed, creating a risk of tire blowouts.
Frito-Lay is recalling specific bags of Lay's Barbecue Flavored Potato Chips because they may contain undeclared milk.
Frito-Lay is recalling 18 count Flavor Mix sacks because they may contain undeclared milk. The product was distributed to retail and foodservice locations in 11 western states.
Frito-Lay is recalling 1,236 bags of Classic Variety Mix and Classic Mix due to potential undeclared milk. The products were distributed to retail and foodservice channels in 11 western states.
Frito-Lay is recalling 54-count Classic Mix cube boxes because they may contain undeclared milk. The product was distributed to retail and foodservice channels in 11 states.
Frito-Lay is recalling 28-count Classic Cube Mix boxes because they may contain undeclared milk. The product was distributed to retail and foodservice channels in 11 western states.
Siemens is recalling Syngo.via RT Image Suite software due to a calibration offset error that could result in incorrect radiation dose or dose applied to the wrong location.
STIHL is recalling about 185,000 mini-cultivator attachments because the gearbox may be installed upside down, causing tines to rotate toward the operator and posing a laceration risk.
BMW is recalling approximately 312 certain 2020-2021 BMW models due to rearview camera software that may slightly obscure the rear view image, potentially increasing crash risk if drivers rely solely on the camera.
LivaNova is recalling 94 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.
ArthroCare Corporation is voluntarily recalling 15,559 units of Smith&Nephew SmartStitch PerfectPasser Connectors because a manufacturing error may cause the upper jaw to detach during use.
LivaNova is recalling 77 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.
BMW is recalling certain 2020-2021 models due to debris in hybrid battery cells that could cause fire or injury. Owners are instructed not to charge vehicles or drive in manual mode.
Irvine Biomedical is recalling 40 units of Inquiry Steerable Diagnostic Catheters because packages were mislabeled with the wrong model and lot numbers, potentially causing procedure delays.
LivaNova is recalling 102 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.
Tesla is recalling 2020 Model Y vehicles with specific configurations because a software error prevents trailer brake lights from illuminating, increasing crash risk.
Perrigo is recalling 7.8 million Albuterol Sulfate inhalers nationwide because the delivery system may fail to dispense the medication.
Petzl is recalling approximately 14,850 low-stretch kernmantle ropes sold in the U.S. and Canada because deep cuts or tape securing rope ends can cause failure, posing fall and injury hazards.
Jayco is recalling 2021 Entegra motorhomes with Villa power seats because the electrical wiring may become damaged or chafed, causing short circuits and fire risk.
Suzuki is recalling 2018 GSX250R and GSX250RZ motorcycles because the headlight may fail, reducing visibility and increasing crash risk.
LivaNova is recalling specific lots of the Perceval Dual Collapser because complaints indicate the device may fail to collapse the heart valve during implantation.
LivaNova is recalling specific lots of Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.
Bio-Rad is recalling BioPlex 2200 Syphilis Total & RPR kits because of increased RPR reactivity levels in the kit material.