State
72,986 recalls have nationwide distribution and so reach New York. 12,906 additional recalls listed New York specifically in their distribution scope.
Of the 12,906 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 3,136 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,906 recalls whose distribution notice names New York specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Altec is recalling 2014-2016 AT200A aerial devices because cracks in the mounting frame legs may cause the side plate to break, increasing injury risk.
American Bolt and Screw recalls tip-over restraint kits distributed with clothing storage units made by Canyon Furniture. The plastic zip ties can become brittle and break, allowing furniture to detach and tip over, posing a risk of serious injury or death to children.
Casely Inc. is recalling Casely Power Pods wireless portable power banks because the lithium-ion battery can overheat and catch fire. The firm has received 51 reports of battery overheating or fire and 6 minor burn injuries.
About 73,000 Joydeco Roller Window Shades sold on Amazon.com have long operating cords that pose strangulation and entanglement hazards to children. The shades violate federal window-covering regulations.
Mercedes-Benz is recalling certain 2025 G 550, G 580 and AMG G 63 vehicles because the electronic stability program may display an incorrect warning light during an ESP system failure.
Honda is recalling 2014-2020 Acura MDX vehicles because moisture can cause interior and exterior lights to fail, increasing crash risk.
Autocar is recalling 2023-2024 Xspotter vehicles because a misrouted alternator ground cable may contact the positive stud, causing damage and increasing the risk of a fire.
Temsa is recalling 2024-2025 TS45 transit buses because the Gross Vehicle Weight Rating on the certification label is incorrect, which may lead to unintentional overloading.
Altec is recalling 2024-2025 Digger Derrick vehicles because an improperly seated retaining ring may cause hydraulic pressure loss and unintended boom movement.
Nissan is recalling certain 2025 Kicks vehicles because the certification label may show incorrect Gross Vehicle and Axle Weight Ratings, and some SR trims may state an incorrect wheel size.
The North Face Women's Shellista V Mid Waterproof Boots are being recalled because the hook on one boot can catch the laces of the other boot, creating a fall hazard. The company has received 28 reports of the hook catching laces, including 15 reports of minor injuries.
Medline Industries is recalling medical procedure kits containing a Medtronic Aortic Root Cannula due to a Class I defect. The kits were distributed to healthcare facilities in nine states.
The Stimulation RC Clinician Programmer Application (Model A71400) has a software issue that can permanently disable communication with certain implantable neurostimulators when a specific intraoperative programming sequence is used. Approximately 1,493 devices were distributed worldwide.
Somerset Therapeutics is recalling Methocarbamol Injection USP (1,000 mg/10 mL vials) nationwide due to lack of assurance of sterility following bacterial contamination in media fill testing.
Zydus Pharmaceuticals is recalling chlorpromazine hydrochloride 10 mg tablets due to the presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit. The recall affects 3,144 bottles distributed nationwide.
Qapel Medical Inc. is recalling the Hippo 072 Aspiration System and related components because the aspiration catheter distal tip may detach, potentially causing vessel rupture or vasospasm.
Somerset Therapeutics is recalling 997 vials of Haloperidol Decanoate Injection 50mg/mL nationwide due to lack of assurance of sterility following bacterial contamination detected in a media fill validation test.
365 Whole Foods Market Small Bites Macaroni & Cheese (8.5 oz) is being recalled because it contains undeclared eggs and pork, which pose a hazard to consumers with allergies.
Somerset Therapeutics is recalling Haloperidol Decanoate Injection 50mg/mL vials nationwide due to lack of assurance of sterility from bacterial contamination detected in media fill testing.
Alchemee LLC is recalling Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%) due to the presence of benzene, a chemical contaminant. The recall affects approximately 38,237 bottles distributed nationwide.
BMW is recalling certain 2025 X3 30 xDrive vehicles because the front brake discs may have been damaged during transport before they were installed on the vehicle.
Medline is recalling medical procedure kits containing a Medtronic Aortic Root Cannula due to potential excess material in the male lures on the cannula. The recall affects 468 units distributed across nine US states.
Somerset Therapeutics is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility resulting from bacterial contamination detected during media fill testing. The recall affects 23,960 vials distributed nationwide.
Medline medical procedure kits containing Medtronic Aortic Root Cannula are recalled due to potential excess material in the male luer connectors on the aortic cannula.
Somerset Therapeutics is recalling Haloperidol Decanoate Injection (100 mg/mL, 1 mL vials) due to lack of assurance of sterility caused by bacterial contamination detected in media fill testing.