State
72,940 recalls have nationwide distribution and so reach New York. 12,903 additional recalls listed New York specifically in their distribution scope.
Of the 12,903 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 3,134 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,903 recalls whose distribution notice names New York specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Dr. Reddy's Laboratories is recalling 4,800 bottles of Varenicline Tablets, 1mg, after the assay value for the affected lot fell below the specification limit at nine-month stability testing.
C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 6 Fr x 30 cm, because the actual stent size may not match the product label.
C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 8 Fr x 26 cm, because the actual stent size may not match the product label.
Stryker is recalling 297 Arise 1000EX mattresses because they and certain MV3 beds have been sold in close proximity, and the two products have not been tested for compatibility.
Winder Laboratories is recalling 3,528 bottles of Morphine Sulfate Oral Solution because the size stated on the carton label did not match the size of the bottle inside.
Orthofix U.S. is recalling 61,977 CONSTRUX Mini PTC Spacer System units because the labeling contains claims that are not consistently present.
Orthofix U.S. is recalling 13,317 Pillar SA PTC Spacer System units because the labeling contains claims that are not consistently present.
Orthofix U.S. is recalling 19,431 FIREBIRD SI Fusion System units because the labeling contains claims that are not consistently present.
Beckman Coulter is recalling 38,225 Access 2 Reaction Vessels because certain lots may have a small protrusion or hair-like deformity that can cause instrument errors and delay patient results.
Datascope is recalling 11,470 Cardiosave Hybrid Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
Datascope is recalling 47 Cardiosave Rescue Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
Toyota is recalling certain 2025-2026 Camry Hybrid and 2026 Corolla Cross Hybrid vehicles because a bolt inside the inverter may not be tightened properly, causing incomplete contact at the terminal.
Gillig is recalling 2025 Low Floor transit buses because wheelchair restraints may fail to lock, posing an injury risk.
Mack Trucks is recalling 2010-2016 Granite trucks because incorrect parts from a previous repair may cause brake overheating, increasing the risk of tire blowouts or fires.
Gillig is recalling 2013 Low Floor transit buses because emergency exit window latches may fail during a crash, increasing injury risk.
Ford is recalling 6,819 model year 2026 Super Duty F-250 and F-350 vehicles because the right rear axle shaft may have been improperly heat-treated and may break.
Ford is recalling 2022-2025 E-Transit vehicles because the left rear axle half shaft may disengage, causing loss of drive power or vehicle rollaway.
Suzanna's Kitchen is recalling fully cooked breaded chicken products because they contain soy, a known allergen, that is not declared on the label.
Diamond Coach is recalling 2025 VIP buses because wheelchair restraints may fail to lock, increasing injury risk during transit.
Mercedes-Benz USA is recalling 82 model year 2025-2026 GLE 350 4MATIC vehicles because center rear seat belts may have been installed without the child seat protection function.
Ford is recalling 272,645 F-150 Lightning, Mustang Mach-E and Maverick vehicles because the integrated park module may fail to lock into park when the driver shifts into park.
Mercedes-Benz USA is recalling 117 AMG E 53 4MATIC+ Wagon vehicles because the transmission wiring harness may be routed too close to the front driveshaft, which can cause a loss of drive power.
Ford is recalling 2025-2026 Corsair and Escape vehicles because rear seat belt retractors may not be securely fastened, increasing injury risk in crashes.
Honda is recalling 2025 CR-V Fuel Cell EVs because coolant may leak into the fuel cell stack, causing an internal short circuit and loss of drive power.
About 2,840 VEVOR Garment Steamers are being recalled because they can leak or spit hot water. Reported cap failures resulted in two burn injuries, including a second-degree burn with permanent scarring.