State
73,741 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.
Of the 12,955 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,701 (29%) are Severe.
Which agencies issued them
These figures cover only the 12,955 recalls whose distribution notice names New York specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer Biomet is recalling 26 units of 13MM Intramedullary Bone Saw Cam Assemblies due to possible commingling with 14MM units.
QuVa Pharma is recalling fentanyl infusion bags because they may contain glass particulates. The affected product is distributed nationwide.
Toyota is recalling 2019 Prius vehicles because an electrical short circuit in the combination meter could cause the speedometer, odometer, and fuel gauge to go blank, increasing crash risk.
Fortune Fish & Gourmet is recalling fresh Atlantic salmon that may be contaminated with Listeria monocytogenes. The product was sold in retail and foodservice locations in eight states.
QuVa Pharma is recalling fentanyl 10 mcg/mL infusion bags nationwide due to the potential presence of glass particulate matter.
Stryker is recalling 16,380 disposable tourniquet cuffs because they may leak air, causing a loss of vascular occlusion during surgery.
Philips is recalling 24,738 HeartStart XL+ Defibrillator/Monitor units because they may fail to turn on or restart, rendering them unable to return to a ready-for-use state.
Porsche is recalling 15,501 vehicles because the owner's manual lacks specific instructions for installing child restraint systems, which may increase injury risk in a crash.
Polaris is recalling 2019 Slingshot models because a defective circuit breaker may cause sudden engine stalls, increasing crash risk.
CooperSurgical is recalling Quantum 2000 Electrosurgical Generators because they may fail to cut, coagulate, or blend during procedures.
QuVa Pharma is recalling specific lots of fentanyl syringes because they may contain glass particulate matter.
Pacira Pharmaceuticals is recalling 910 vials of Exparel (Bupivacaine) because the drug was found to be sub-potent and out of specification.
NDDd Medical Technologies is recalling 37 EasyOne Pro Respiratory Analysis Systems because the CO/CO2 sensor cable harness may have insufficient electromagnetic shielding.
NDDd Medical Technologies is recalling 37 EasyOne Pro LAB VOS devices due to potential non-compliance with electromagnetic shielding standards.
Brasseler USA is recalling 387 units of 3.5 mm twist drills that were incorrectly laser etched as 2.5 mm.
Miami Device Solutions is recalling 15 units of Right Proximal Humerus Plates because they may be improperly identified as left.
Theralase Inc. is recalling 41 TLC-2000 Therapeutic Medical Laser Systems because they were shipped without required Unique Device Identification (UDI) labels.
Theralase Inc. is recalling 306 TLC-2002 Power Packs for the TLC-2000 Therapeutic Medical Laser System because they were shipped without a Unique Device Identification (UDI) label and incorrectly labeled as CE Marked.
Ruiz Food Products is recalling approximately 55,013 pounds of frozen breakfast burritos that may contain pieces of plastic. No injuries have been reported.
Bass Pro is recalling MR. STEAK four and five burner gas grills because the fuel line can melt and cause a fire.
Marion Body Works is recalling 2018-2019 Spartan Gladiator and Metro Star emergency response chassis because a brake relay valve defect may cause extended stopping distances.
Jayco is recalling 2019-2020 White Hawk travel trailers because the rear emergency escape window cannot fully open due to a ladder. Owners should contact dealers for a free repair.
Keystone RV Company is recalling 2020 Springdale trailers because the Federal Identification Tags list incorrect rim, tire, and pressure information.
ARBOC Specialty Vehicles is recalling 2017-2019 Spirit of Freedom and Spirit of Mobility vehicles because the roof hatch handle may break, preventing emergency egress.
Proterra is recalling 2019 Catalyst buses because a software update may have disabled brake interlock warnings, increasing the risk of fire or crash.