State
72,913 recalls have nationwide distribution and so reach New Mexico. 3,625 additional recalls listed New Mexico specifically in their distribution scope.
Of the 3,625 recalls naming New Mexico we have scored against our rubric, 747 (21%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 647 (18%) are Severe.
Which agencies issued them
These figures cover only the 3,625 recalls whose distribution notice names New Mexico specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
BenQ GV31 portable projectors can overheat because of their lithium-ion battery. The firm has received three overheating reports, one of which caused burns to a consumer's hands.
About 1,980 KAIFAM 5-drawer metal dressers sold on Amazon are unstable when not anchored to a wall and violate the STURDY Act standard. No injuries reported.
An additional 195 Cpzzkq baby loungers are recalled because the padding can obstruct an infant's breathing, breaching the mandatory infant support cushion standard. No injuries reported.
HARPPA recalled 47,166 Nordi foldable toddler tower stools that can collapse or tip over, with openings a child's torso can pass through. Three incidents and two minor injuries reported.
Joyin expanded its recall of Sloosh dive sticks to models 40003 and 16154 alongside model 40041. The sticks exceed the federal compression limit and pose an impalement hazard. No injuries reported.
105 Mangohood Direct children's tower stools, model LT003, can collapse or tip over, and a child's torso can fit through openings on the front and back. No injuries reported.
About 55,350 Fantastic Four drinking cups and Captain America popcorn helmets with LED lights have accessible button cell batteries and lack the warning labels required by Reese's Law.
About 1,034 Mommy's Baby Lovely Deluxe Baby Doll Playsets sold on Temu contain small parts that pose a choking hazard to children under three. No injuries reported.
Autocar is recalling 2023-2027 ACTT terminal tractors because the ABS Electronic Control Unit may be improperly secured, potentially causing system failure and increasing crash risk.
Jake's Fireworks recalled about 132,440 World Class Fireworks "Skull Strobe" rockets because they can explode before reaching their intended height. No injuries have been reported.
Brinkley RV is recalling 2027 Model I trailers because the exterior ladder may not be properly secured, posing a risk of injury if it detaches.
About 91,000 Woodure toddler tower stools can collapse or tip over, with openings a child's torso can pass through. Woodure reports 22 incidents and 15 injuries involving scrapes, cuts and bruises.
JB Chemicals and Pharmaceuticals Ltd is recalling 34,020 bottles of Cetirizine Hydrochloride Tablets USP 5 mg because some tablets were found to contain Ranitidine due to cross contamination.
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets, 75 mcg, NDC 0904-6951-61, due to subpotency. The recall affects lots N02172, N02296, and N02288 with expiration dates in July and December 2026, distributed nationwide.
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium 125 mcg tablets (Lot N02266, Exp. 11/2026) nationwide due to subpotency, meaning the tablets may contain less active ingredient than labeled.
Hyundai is recalling 2027 Genesis G80 vehicles because a loose ignition coil ground bolt may cause engine misfires or stalls, increasing crash risk.
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 50 mcg, due to subpotency. The recall affects nationwide distribution in the USA and involves specific lot numbers.
The FDA is recalling ROHTO OPTIC GLOW sterile eye drops due to a lack of assurance of sterility. The recall affects 1,278,457 cartons distributed nationwide in the U.S.
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 150 mcg, lot N02167, due to subpotent drug concerns. The recall affects nationwide distribution in the USA.
Modern Warrior Life, LLC is recalling Modern Warrior Ready dietary supplements because they contain unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 25 mcg, due to subpotency. The recall affects nationwide U.S. distribution of specific lot numbers.
Total Nutrition Inc is recalling TNVitamins 100% Organic Moringa Capsules and Powder due to Salmonella contamination. The recall affects 8,492 units distributed nationwide.
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 88 mcg, lot N02310, due to subpotency. The recall is voluntary and affects nationwide distribution in the USA.
The FDA is recalling 278 Power F2 Powered Fastening Systems made by Ferno-Washington Inc due to potential roller wear and rail deformation that could prevent stretcher movement.
Rohto Digi-Eye cooling eye drops are recalled due to a lack of assurance of sterility. The recall affects 65,219 cartons distributed nationwide in the U.S.