State
73,806 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.
Of the 12,956 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 3,702 (29%) are Severe.
Which agencies issued them
These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Philips is recalling 3,177 SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.
Volkswagen is recalling 2012-2020 Passat and 2018-2019 Atlas vehicles because a missing blocking cap allows headlight aim to be adjusted out of specification, increasing crash risk.
Philips is recalling 366 SureSigns VS4 monitors because software prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Shippert Medical Technologies is voluntarily recalling 6,553 units of Tissu-Trans FILTRON 2000 sterile, disposable, one-patient use devices due to a Class II classification.
Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 sterile pouches because a cut or hole may compromise sterility.
Philips is recalling 518 SureSigns VS3 monitors because a software defect prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Abbott is recalling ARCHITECT Estradiol Reagent Kits because patient results may be falsely elevated for individuals currently or recently treated with Mifepristone.
Stryker is recalling 3,285 Power-LOAD Cot Fastening Systems because the floor plates holding ambulance cot anchors may be broken.
Philips is recalling SureSigns VS4 monitors because software prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Shippert Medical Technologies is recalling Tissu-Trans FILTRON 250 sterile filters because the pouch integrity cannot be assured without visual examination.
Arctic Cat is recalling about 1,700 Textron Havoc recreational off-highway vehicles because upper front suspension arms can fail, posing a crash hazard.
PENTAX of America Inc is recalling 4 C2 CryoBalloon Catheters because incorrect default doses and increments may be transmitted to the controller if the RFID tag is not correctly readable.
AmeriHerb International Inc is recalling 108 lbs of Blessed Thistle herb due to potential contamination with generic E. coli. The product was distributed nationwide and to Canada.
AmeriHerb International Inc is recalling 103 lbs of Lemon Balm Leaf due to potential E. coli contamination. The product was distributed nationwide and to Canada.
Philips is recalling SureSigns VS3 NBP monitors because software prevents the display and alarm for pulse rates above 240 beats per minute.
Siemens is recalling 459 Artis Q angiography systems because the floating tabletop may become blocked after a collision sensor activates.
Unipharma is recalling CVS Health Children's Pain & Fever Acetaminophen single-use vials due to a precautionary measure regarding potential contamination with B. cepacia bacteria.
Associates of Cape Cod, Inc. is recalling Fungitell Kits due to potential missing or incorrect components.
Unipharma, LLC is recalling 280 cartons of DrKids Children's Pain & Fever Oral Solution due to potential contamination with B. cepacia bacteria.
Back Roads Food Company is recalling specific lots of Ancient Grains Granola because the products may contain pieces of aluminum.
Unipharma, LLC is recalling CVS Health Children's Mucus Relief Chest Congestion Plus Cough due to potential contamination with B. cepacia bacteria.
Unipharma is recalling CVS Health Children's Cough & Chest Congestion DM due to potential contamination with B. cepacia bacteria.
Barlean's is recalling Cod Liver Oil softgels due to undeclared sulfites. Sulfite levels do not exceed 10 ppm.
Back Roads Food Company is recalling specific lots of Gluten-Free Granola because the products may contain pieces of aluminum.
Compass Health Brands is recalling MediPress pneumatic compression systems because a product design change lacked proper FDA premarket clearance.