State
72,907 recalls have nationwide distribution and so reach New York. 12,902 additional recalls listed New York specifically in their distribution scope.
Of the 12,902 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 3,133 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,902 recalls whose distribution notice names New York specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 50 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.
Lidl US Trading is recalling Eridanous Greek Style Shortbread Cookies because the labels contain only foreign languages and fail to declare wheat, soy, milk, eggs, and coconut.
Fresenius Medical Care is recalling 1,140 BlueStar Hemodialysis machines due to reported flow, water, or temperature-related alarms.
Merge Healthcare is recalling 20 Merge PACS and Merge OrthoPACS workstations because a software issue may cause measurements to be displayed inaccurately.
Medline Industries is recalling 663 surgical convenience kits distributed nationwide because they contain a potentially contaminated component.
Toyota is recalling specific 2024-2026 models because inaccurate load capacity labels may lead to vehicle overloading and increased crash risk.
Lidl US Trading is recalling 200 units of Eridanous Greek Style Shortbread Cookies because the labels contain only foreign languages and fail to declare wheat, soy, milk, eggs, and coconut.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 25 mcg tablets nationwide because they are subpotent.
Byron White Formulas is recalling A-L Complex Herbal Supplement because the label does not declare walnuts in English, posing a risk to individuals with nut allergies.
Medline Industries is recalling 241 neurosurgical convenience kits distributed nationwide because they contain a potentially contaminated component.
Byron White Formulas is recalling its A-P Herbal Supplement because the label fails to declare walnuts in English, posing a risk to individuals with nut allergies.
Healthmark Industries is recalling ProChek-II tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
GE Medical Systems is recalling Portrait Core Services Software V1.1 because a software issue may cause loss of patient monitoring and reset alarm settings to factory defaults.
Medline Industries is recalling 1,349 gynecologic robotic surgery kits nationwide because they contain a potentially contaminated component.
Medline is recalling 145,525 neonatal and infant heated wire breathing circuits due to potential thermal damage that could cause airway obstruction.
IMRIS Imaging Inc is recalling 13 ORT300 operating room tables because a mechanical failure could cause unintended rotational movement, posing a risk of injury to patients.
Medline Industries is recalling 169 surgical convenience kits nationwide because they contain potentially contaminated components.
Kettle Cuisine is recalling Marketside Tomato Bisque Soup Kits due to a presumptive positive test for Listeria monocytogenes.
GE Medical Systems is recalling 15 units of Portrait Core Services Software V1.0.5 because a software issue may cause loss of patient monitoring and reset alarm settings to factory defaults.
Medline is recalling 24 convenience kits labeled as MAJOR HEAD AND NECK PPS because they contain a potentially contaminated component.
Medline is recalling 974 neurosurgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Medline Industries is recalling 15 convenience kits (SKU CDS980375M) due to a potentially contaminated component. The kits were distributed in 18 US states.
Healthmark is recalling ProChek protein tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Midmark is recalling Digital ECG HD+12 and HD+15 units with specific IQecg plugin software versions due to a communication anomaly that may cause incorrect ECG waveforms and inaccurate heart rate calculations.
Medline Industries is recalling 71 FEMORAL PACK and FEVAR convenience kits because they contain a potentially contaminated component.