State
72,966 recalls have nationwide distribution and so reach New York. 12,905 additional recalls listed New York specifically in their distribution scope.
Of the 12,905 recalls naming New York we have scored against our rubric, 1,501 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,135 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,905 recalls whose distribution notice names New York specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 200 DINBooonLUX 12-inch full size hybrid mattresses are being recalled because they violate the mandatory flammability standard.
About 8,850 Grundens Youth Clipper 282 and Zenith 282 jackets are being recalled because the hood drawstring can catch on objects and strangle a child.
About 5,340 mattresses marketed under the Avenco and Novilla brands are being recalled because they violate mandatory flammability standards.
KTM North America is recalling 5,488 2024 KTM and Husqvarna motorcycles because the fuel filler cap seal may crack and leak fuel, increasing the risk of fire or injury.
Toyota Motor Engineering & Manufacturing is recalling 2022–2026 Toyota, Lexus, and Subaru vehicles with a Panoramic View Monitor system due to a software error that may freeze or blank the rearview camera in reverse, reducing rear visibility and increasing crash risk.
Autocar is recalling 2025-2026 Xpeditor vehicles because the Automatic Emergency Braking system may unexpectedly turn off when the vehicle turns, increasing crash risk.
Braun is recalling wheelchair restraint retractors on specific Chrysler, Toyota, and Honda minivans because they may not lock, increasing injury risk.
Kia is recalling certain 2025 Telluride and 2026 Sorento vehicles due to an incorrect spare tire that can impair the anti-lock braking and traction control systems, increasing crash risk.
Remote Vans is recalling 2025 Aegis and Oasis motorhomes because optional equipment may cause the vehicles to exceed their Gross Vehicle Weight Rating, increasing crash risk.
About 4,300 Harppa 5-in-1 convertible high chairs are being recalled because they were sold without the required restraint system and a child's head can become trapped between seat and tray.
About 6,880 YaFiti fabric 12-drawer dressers are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.
About 6,600 Destination Holiday Glow Light Stick bracelet 12-packs are being recalled because the green bracelet can leak, posing a skin irritation hazard.
M.C.I. Foods is recalling 330 cases of Cheese and Egg with Green Salsa Breakfast Burritos after the cooked egg ingredient tested positive for Listeria monocytogenes.
Twin Marquis is recalling 5,080 packages of Thick Shanghai Style Plain Noodle because the product contains undeclared egg, FD&C Yellow 5 and FD&C Yellow 6.
Turkana Food is recalling 352 cases of Floria Dried Apricots because the product contains undeclared sulfites.
B. Braun is recalling Streamline Bloodline Sets for Dialog because damaged arterial and venous patient connectors may cause micro-air bubbles in the bloodline and air-in-line alarms.
Demers Food Group is recalling 12,962 cases of Scott & Jon's Shrimp Scampi with Linguine because it contains linguine recalled for Listeria monocytogenes and implicated in an ongoing outbreak.
M.C.I. Foods is recalling 1,040 cases of Egg and Cheese Breakfast Burritos and Wraps after the cooked egg ingredient tested positive for Listeria monocytogenes.
ICU Medical is recalling 23,203 IV administration sets because the burette component is missing an internal shutoff valve intended to stop fluid flow.
Abiomed is recalling Automated Impella Controllers over the potential for purge pressure issues caused by purge retainer failures, covering 9,177 distributed units.
Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.
Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.
Cardinal Health is recalling all lots of Salem Sump silicone dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Medline is recalling 8,267,150 Excelsior Medical 0.9% Sodium Chloride prefilled flush syringes because a limited quantity may not meet the required concentration of sodium chloride.
Theken Companies is recalling 409 iNSitu Bipolar Hip System head assemblies in a downstream recall after BioPro femoral components failed transit testing, risking sterile barrier issues.