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.
Mercedes-Benz is recalling one 2020 GLE 350 because a driver's seat bolt may not be installed correctly, which could increase injury risk in a crash.
PACCAR is recalling 2020 Peterbilt 520 trucks because incorrect bolts may allow the steering assist bracket to loosen, potentially locking the steering.
Kiel is recalling Avance coach seats because the automatic locking retractor mode of the seat belts cannot be activated, increasing injury risk in crashes.
Great Dane is recalling 2018-2020 Truck Bodies because the license plate light may aim rearward, failing federal safety standards and increasing crash risk.
Keystone Fuzion and Impact toy hauler travel trailers may have incorrectly wired generator transfer switches that could energize the shore power connection, creating an electrical shock hazard. Keystone will inspect and correct the wiring at no charge.
Polaris is recalling approximately 13,200 Ranger, PRO XD, and Bobcat utility vehicles because a defective clutch component can cause unexpected motion, posing a crash hazard.
Willis Electric is recalling Home Accents Holiday artificial Christmas trees sold at Home Depot because the foot-pedal controller can overheat and cause burns.
Bulk Apothecary is recalling Nature's Oil Wintergreen and Birch Essential Oils because the packaging is not child-resistant, posing a poisoning risk to young children.
CME America is recalling BodyGuard BodySet infusion sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.
CME America, LLC is recalling BodyGuard Microset infusion sets because they may deliver therapy with significant inaccuracy, potentially causing over-infusion or under-infusion.
CME America is recalling BodyGuard Microset infusion administration sets due to delivery inaccuracy that may cause over-infusion or under-infusion of therapy.
CME America is recalling BodyGuard Microset infusion sets because delivery inaccuracy could cause over-infusion or under-infusion of therapy.
CME America, LLC is recalling BodyGuard Microset infusion administration sets because they may deliver therapy with an inaccuracy exceeding plus/minus 13%, potentially causing over- or under-infusion.
CME America is recalling CMExpress Microbore Sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.
Skeletal Kinetics is recalling 41 units of Acumed Impact 5CC bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.
CME America is recalling Standard BodySet infusion sets because they may deliver therapy at inaccurate rates, potentially causing over- or under-infusion.
CME America is recalling CMExpress Microbore Sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.
CME America is recalling BodyGuard Microset infusion sets due to delivery inaccuracies that may cause over- or under-infusion of therapy.
Skeletal Kinetics is recalling Craniosculpt Flow bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.
CME America, LLC is recalling CMExpress Microbore Sets because they may deliver fluids with significant inaccuracy, potentially causing over-infusion or under-infusion of therapy.
CME America is recalling BodyGuard Microset infusion administration sets due to delivery inaccuracy that could cause over-infusion or under-infusion of therapy.
CME America is recalling BodyGuard Microset infusion sets because they may deliver fluid at inaccurate rates, potentially causing over- or under-infusion of therapy.
Skeletal Kinetics is recalling Medtronic Bone Void Filler kits that may not maintain setting characteristics, potentially increasing surgical time or causing bone formation issues.
CME America is recalling BodyGuard Microset infusion administration sets due to delivery inaccuracy that could cause over-infusion or under-infusion of therapy.
CME America is recalling BodyGuard Microset infusion administration sets because they may deliver therapy with significant inaccuracy, potentially causing over-infusion or under-infusion.