State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Toyota is recalling specific Lexus and Land Cruiser vehicles because they may have incorrect air bags that could fail to deploy in a crash.
Hallmark is recalling itty bittys baby plush stacking toys because fabric hats and bows can detach, posing a choking hazard to children.
Chrysler is recalling 2017-2018 Pacifica minivans with 8-passenger seating because a seat belt buckle may cause the left outboard belt to unlatch.
C. O. Truxton is recalling Phenobarbital 15 mg tablets that were actually 30 mg due to a labeling error.
Demakes Enterprises is recalling 32,228 pounds of chicken sausage because it contains undeclared milk, a known allergen.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 30 mg, because they may be mislabeled. The FDA classifies this as a Class I recall.
Commonwealth Dairy is recalling Friendly Farms Key Lime Crunch Tilts Greek Lowfat Yogurt because it may contain undeclared almond pieces.
Bush Brothers & Co is recalling 28-ounce cans of Country Style Thick, Rich Sauce with Bacon & Extra Brown Sugar due to defective side seams that may allow C. botulinum growth.
Solta Medical is recalling four VASER Amplifier units because a service depot repair may have caused inaccurate calibration, posing a burn risk to patients.
Erwin Hymer is recalling 2016-2018 Hymer Aktiv recreational vehicles because the exhaust pipe may melt the rear bumper and wiring, increasing crash and burn risks.
The Harvard Drug Group is recalling Rugby Diocto Liquid due to microbial contamination, including yeast and potential B. cepacia.
Bush Brothers & Co is recalling Bush's Best Baked Beans due to defective side seams that may allow C. botulinum growth.
The Harvard Drug Group is recalling Major Senna Syrup due to microbial contamination, including yeast and potential B. cepacia.
Bush Brothers & Co is recalling Bush's Best Brown Sugar Hickory Baked Beans due to defective side seams that may allow C. botulinum growth.
The Harvard Drug Group is recalling Rugby Diocto Syrup due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling 4,715 bottles of Rugby Aller-chlor syrup due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling Rugby Senexon Liquid due to microbial contamination, including yeast and potential B. cepacia.
Medtronic is recalling 60 reusable ENT suction instruments because they fail required pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Custom Assemblies Inc is recalling 2,155 custom surgical kits because they contain BD SafetyGlide needles with loose polypropylene particulate in the fluid path.
Penobscot McCrum LLC is recalling Sysco X-Large Jo-Jo Wedges because the product may contain undeclared milk.
Fresh Venture Foods is recalling Gold Coast Packing Broccoli Florets due to potential E. coli contamination found in firm test results.
Penobscot McCrum LLC is recalling Extra Large Coated Jo-Jo Wedges because the product may contain undeclared milk.
REV is recalling 2018 Fleetwood Jamboree and Holiday Rambler Vesta motorhomes because improperly stripped generator wires may cause an electrical short and fire.
Shippert Medical Technologies is recalling Tissu-Trans SFILL 360 devices because the seal integrity of the sterile packages cannot be assured.
Alcon is recalling 429 ORA Systems with VerifEye+ Carts due to a software error that may cause incorrect intraocular lens power measurements during cataract surgery.