State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Camp Chef is recalling about 20,600 portable gas stoves because a sharp edge on an internal gas regulator part can cause gas leaks, posing a fire hazard.
Medtronic is recalling 71,030 Evolut PRO System units worldwide due to a potential for transcatheter aortic valve leaflet damage during post-implant balloon dilatation.
Mani, Inc. is recalling Trocar Kit 23G S units because Luer connector dimensions are out of specification, which may cause fluid leakage or disconnection during ophthalmic surgery.
Graco is recalling inclined sleeper accessories for four playard models due to a risk of infant suffocation. Consumers should stop using the accessory immediately and contact Graco for a refund.
Philips is recalling 16 IntelliVue X2 Multi Measurement Servers because speaker failures may prevent audible alarms, potentially delaying patient treatment.
Shimadzu Medical Systems is recalling 22 MH-200S X-Ray systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.
Medtronic is recalling Evolut R System transcatheter aortic valves due to a potential risk of leaflet damage during post-implant balloon dilatation.
K2M, Inc. is recalling 197 units of the Everest MI XT Tab Removal Tool because the threaded interface may crack, causing Loctite to leak from the handle.
JMH International is recalling Chef Myron's Szechuan Sauce because it contains wheat-derived fermented soy sauce despite a gluten-free claim.
Medtronic is recalling 19,961 Evolut PRO+ Transcatheter Aortic Valve systems due to a potential for leaflet damage during post-implant balloon dilatation.
Chromsystems Instruments & Chemicals GmbH is voluntarily recalling 342 vials of MassChrom Amino Acid Analysis Plasma Control Level III due to a Class II device defect.
Cycling Sports Group is recalling about 1,270 Cannondale Canvas NEO e-bicycles because the front fender can detach and stop the wheel, posing a fall hazard.
Mani, Inc. is recalling MANI Infusion Cannula 23G S units because Luer connector dimensions are out of specification, which may cause fluid leakage or unintended disconnection during ophthalmic surgery.
TissueTech, Inc. is recalling 10 units of PROKERA Plus non-sterile biologic corneal bandages due to potential exposure to microbial contamination.
Riverside Natural Foods is recalling Good & Gather Banana Chocolate Chip Date & Nut Bars because they contain undeclared almonds.
Philips is recalling two IntelliVue MP2 patient monitors because speaker failures may prevent audible alarms, potentially delaying patient treatment.
TissueTech, Inc. is recalling 75 units of PROKERA Slim non-sterile biologic corneal bandages due to potential exposure to microbial contamination.
Chromsystems Instruments & Chemicals GmbH is recalling MassChrom Amino Acid Analysis Plasma Control Level I kits because they do not meet stability criteria and may impact results.
JMH International is recalling Chef Myron's Premium Shoyu Sauce because it contains wheat-derived gluten despite a gluten-free claim.
BRP is recalling Can-Am Off-Road screw jacks because they can collapse, posing a crush hazard that could cause severe injury or death.
Randox Laboratories is recalling four kits of the Rx Series Mg Magnesium test due to reduced linearity performance.
Shimadzu Medical Systems is recalling 115 Mobile X-Ray Systems because the adjustable handle may have improper bolts, posing a risk of harm to individuals around the device.
Shimadzu is recalling 23 Trinias Digital Angiography Systems because a software defect may cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.
Shimadzu Medical Systems is recalling seven Bransist Safire Digital Angiography Systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm.
Aston Martin is recalling 151 2021 DBX vehicles because they were built without required headliner foam blocks, increasing injury risk in crashes.