State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lipari Foods is recalling Old Tyme Colby Cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Old Tyme Swiss Cheese due to potential Listeria monocytogenes contamination from a supplier.
Saputo Cheese USA is recalling Great Midwest Applewood Smoked Gouda Cheese because it may be contaminated with Listeria monocytogenes.
Philips is recalling HeartStart MRx Monitor/Defibrillators because they may fail to deliver therapy or monitoring when operating on a single battery.
Lipari Foods is recalling Old Tyme Colby Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.
Gourmet Kitchen, Inc. is recalling French Toast with Strawberries & Mascarpone because the frozen strawberries may be contaminated with Hepatitis A.
Claris Lifesciences Inc. is recalling 72,072 units of Metronidazole Injection, USP, 500 mg/100 mL, due to a potential leak that may compromise sterility.
E-One is recalling 2013-2016 Quest, Typhoon, and Cyclone II emergency vehicles because front suspension ball joints can loosen and separate, potentially causing a loss of steering control.
Mylan Pharmaceuticals is recalling specific lots of Atorvastatin Calcium 10 mg tablets due to potential microbial contamination and elevated bioburden.
Merit Medical Systems is voluntarily recalling 1,265 units of 7F Prelude Short Sheath Introducers because the sheath marker tips may detach during use.
Freshbev LLC is recalling Sweet Green Juice due to elevated patulin levels. The product was distributed in five states.
Freshbev LLC is recalling 5-gallon apple juice and 2-oz immunity shots due to elevated patulin levels. The products were distributed in five states.
Mylan Pharmaceuticals is recalling Atorvastatin Calcium Tablets, 80 mg, due to potential microbial contamination and elevated bioburden.
Lipari Foods is recalling Old Tyme Firecracker Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Old Tyme Muenster Cheese due to potential Listeria monocytogenes contamination from a supplier.
Mylan Institutional, Inc. is recalling 1,527 cartons of Atorvastatin Calcium 10 mg tablets due to potential microbial contamination and elevated bioburden.
Stryker is recalling 292 Visum LED Surgical Lighting systems because missing screws and user overloading may cause the equipment to fall.
Tiffin is recalling 2017 Allegro Breeze motorhomes because front suspension ball joints can loosen, potentially causing a loss of steering control.
Claris Lifesciences Inc. is recalling Levofloxacin Injection due to a potential leak that may compromise sterility. The recall covers 24,456 units distributed nationwide.
Claris Lifesciences Inc. is recalling Ciprofloxacin in Dextrose Injection due to a potential leak that may compromise sterility.
Claris Lifesciences is recalling Fluconazole Injection due to a potential leak that could compromise sterility and contaminate the product.
National Biological Corp is recalling seven Hand Foot II, UVB-138 phototherapy devices because wiring defects may allow lamps to turn on with the key switch rather than the timer.
Hospira is recalling 62,847 Plum 360 Infusion Pumps with software version 15.02 due to a defect that causes therapy to stop and incorrect alarms to display.
Merge Healthcare is recalling iConnect Enterprise Archive software because archived studies cannot be opened or sent to PACS, preventing physicians from reviewing comparison studies.
Merge Healthcare is recalling iConnect Enterprise Archive software versions that may fail to display prior medical images, potentially delaying treatment.