State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Good Fields Farm/The Maiden's Creamery is recalling Wild Meadow Raw Goat Milk Cheese after a sample tested positive for Listeria monocytogenes in New York.
BMW is recalling 2007-2012 models because a failing electric auxiliary water pump can overheat the circuit board, increasing the risk of a fire.
Bob's Red Mill Natural Foods is recalling Organic Whole Grain Amaranth Flour due to potential Salmonella contamination. The product was distributed in ten US states, Mexico, and the UAE.
Fresenius Medical Care is recalling Liberty Select Cyclers due to a software issue that may cause overfill, posing a risk of serious injury or death.
Volkswagen is recalling 2006-2007 Passat sedans and wagons because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.
W & H DentalWerk is recalling S-N1 and S-N2 foot controls because they may fail to stop the motor, posing a risk of serious patient injury.
Terumo is recalling 2,677 Cardiovascular Procedure Kits containing Pall LG6NS filters due to a risk of blood leaks through the hydrophobic portion.
Reliance Medical Products is recalling 933 Refractor Suspension Arms because missing parts caused the device to fall on a patient.
Poppies International is recalling three brands of frozen Belgian mini eclairs because they may be contaminated with Listeria monocytogenes.
ICU Medical is recalling 250 pouches of 7-inch intravascular administration sets because they were manufactured with an incorrect spin collar.
Teleflex Medical Europe Ltd is recalling 107,962 latex rebreathing bags because they lack the required warning that the product contains natural rubber latex, which may cause allergic reactions.
C.R. Bard is recalling specific lots of Bard Adult/Pediatric Feeding Tubes because the tubing and ENFit connector may not be fused effectively.
Newmar is recalling specific 2013-2017 motorhomes because low beam headlights turn off when high beams are activated, reducing driver visibility.
Getinge is recalling 5,214 VOLISTA StandOP surgical lights because the central handle holder can detach, potentially dropping particles into the sterile field during procedures.
C.R. Bard is recalling 23,400 infant feeding tubes because the tubing and connector may not be effectively fused.
Beckman Coulter is recalling 288 AQUIOS CL Flow Cytometer Systems because the single tube loader may process the same sample with two different IDs, potentially causing erroneous results.
Primark is recalling about 14,500 decorative cushions sold in the northeastern U.S. because they can catch fire if exposed to an ignition source.
Hill-Rom is recalling 2,117 Progressa adjustable hospital beds because a braking system component may break, causing unwanted bed movement and potential injury.
Riverside RV is recalling 2015-2017 White Water, Water Fall, and Mt. McKinley motorhomes because certain fire extinguishers may clog or detach, posing injury risks.
C.R. Bard is recalling specific lots of Bard Premature Infant Feeding Tubes because the tubing and ENFit connector may not be effectively fused.
Beckman Coulter is recalling iQ200 Series Urine Microscopy Analyzers because they may fail to read dilution barcodes, causing erroneous results that could delay treatment.
C.R. Bard is recalling 42,200 units of Bard Premature Infant Feeding Tubes due to potentially ineffective fusion between the tubing and the ENFit connector.
Elroselabs Inc. is voluntarily recalling Molleave, 2 oz bottles, due to current Good Manufacturing Practice (cGMP) deviations. The product was distributed nationwide.
ICU Medical is recalling 7,600 sterile intravascular administration sets because they were manufactured with an incorrect spin collar. The sets were distributed in the US, Canada, and Japan.
Elroselabs Inc. is voluntarily recalling Conzerol Hydrogen Peroxide Gel 3% nationwide due to current Good Manufacturing Practice (cGMP) deviations.