State
72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pentax Medical EPK-i8020c video processors are recalled after reports of darkened images, smoke-like steam and a hot endoscope light guide that may cause thermal injury to the patient's mucous membrane. 144 units are affected.
Estrone RIA kits, catalog number DSL8700, are recalled because certain lots may rarely give falsely high or falsely low patient results. 279 units are affected.
Burr Hole Cover Kits used with the Vercise Deep Brain Stimulation System are recalled because resistance closing the retaining clip may cause procedural delay or lead migration requiring further surgery. 24,583 units are affected.
BZK Antiseptic Towelettes containing benzalkonium chloride 0.13%, sold 100 per carton for professional use, are recalled for lack of assurance of sterility. The recall covers 3.85 million cartons.
Hospira 8.4% Sodium Bicarbonate Injection USP, 50 mEq/50 mL, lot LH2671, is recalled nationwide for lack of assurance of sterility. 15,750 vials are affected.
Carvedilol Tablets USP, 12.5 mg, packaged by Major Pharmaceuticals, lot T05693, are recalled nationwide because N-Nitroso Carvedilol Impurity-1 exceeded the FDA-recommended 4.0 ppm limit. 26,628 cartons are affected.
Hospira Epinephrine Injection USP, 1 mg/10 mL, lots LY3681, LY4360 and LY4416, is recalled nationwide for lack of assurance of sterility. 49,620 vials are affected.
The ESG-410 Legacy Electrosurgical Generator, model WA91307C, is recalled because it may display an E0662 System Error followed by a single automatic reboot or a continuous reboot loop. 434 units are affected.
DRS Vascular is recalling 264 Q-Stop Suture Retention Devices. The FDA enforcement record for this action carries a placeholder in place of a stated reason for the recall.
Dynex Agility Sample Tips, model 67910 lot 863366, are recalled because the internal rack label reads reagent tip rack, causing the instrument to misidentify the tips and preventing their use. 237 units are affected.
Clearview Strep A Exact II Dipstick Respiratory Kits are recalled because a classification error in the inventory system sent devices to customers without the required license to buy them. 5 kits are affected.
Tavaborole Topical Solution 5%, 10 mL bottles from lot T401968, distributed by Viona Pharmaceuticals, is recalled because of discoloration. 3,960 bottles are affected.
Cipla Albuterol Sulfate Inhalation Aerosol, 90 mcg, lot 4IB0519, is recalled nationwide after out-of-specification particle size distribution results at the 12-month stability point. 20,352 packs are affected.
VITROS Chemistry Products Ca Slides, catalog number 145 0261, generations 67 and above, are recalled because calibration failures on VITROS XT systems delay calcium test results. 174,215 units are affected.
Sensodyne Pronamel Active Shield toothpaste is recalled for a label mix-up: the outer carton reads Fresh Mint while the tube reads Cool Mint/Whitening. The toothpaste inside is Fresh Mint, as the carton states.
Forest River is recalling certain 2018-2026 Riverstone fifth wheel trailers because the steel hydraulic brake lines may fail and leak brake fluid, causing a loss of brake function.
Polestar is recalling certain 2025 Polestar 3 vehicles because the hood wing front bumper may be missing bolts, allowing the bumper to detach and become a road hazard.
Chrysler is recalling specific Mopar rearview camera modules because cracks in the microprocessor may prevent the image from displaying properly, increasing crash risk.
Forest River is recalling 2026 Cedar Creek recreational trailers because they may lack an emergency exit window, posing a risk of injury during an emergency.
Chrysler is recalling certain 2019-2021 Ram ProMaster and 2019-2020 Dodge Journey vehicles because cracks in the microprocessor may stop the rearview camera image displaying properly.
Tiffin Motorhomes is recalling 2025 GT1 Touring vans because rear seat belt buckles may be too short to fasten, increasing injury risk in a crash.
Nova Bus is recalling 2013 LFS transit buses because coolant hoses may leak hot liquid into the passenger area, posing a burn risk.
Hyundai is recalling certain 2025–2026 Tucson and Santa Fe vehicles because engine connecting rod bolts may have been improperly tightened, risking loss of drive power, engine damage, oil leaks, and potential fire.
Keystone RV Company is recalling 2026 Springdale and Hideout travel trailers because pivot brackets on the bunk bed may bend or break, posing a risk of injury.
Kia is recalling certain 2025 K4 and Sorento vehicles because the connecting rod bolts in the engine may have been improperly tightened, which can cause a loss of drive power.