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.
Channel Fish Processing Co. Inc. is recalling Diamond Chef Raw Breaded Natural Flounder Fillets because they contain undeclared milk, a major allergen.
Channel Fish Processing Co. Inc. is recalling raw breaded fish squares due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling Pacific Dynasty Raw Breaded Cod Squares due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling Sea Best Raw Breaded Cod Squared due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling raw breaded cod tails because they contain undeclared milk, a major food allergen.
Channel Fish Processing Co. Inc. is recalling raw breaded swai fillets because they contain undeclared milk, a major food allergen.
Channel Fish Processing Co. Inc. is recalling ICYBAY Raw Breaded Natural Flounder Fillets due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling ICYBAY Raw Breaded AK Pollock Square due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling raw breaded flounder portions because they contain undeclared milk, a major food allergen.
Channel Fish Processing Co. Inc. is recalling Checkers/Rally's Fish Breaded due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling raw breaded haddock tails because they contain undeclared milk, a major food allergen.
Fisher Diagnostics is recalling specific lots of Pacific Hemostasis FDP Latex Reagent because reduced sensitivity may cause false negative test results.
Channel Fish Processing Co. Inc. is recalling Channel Brand Panko Breaded Tilapia because the product contains undeclared milk, a major food allergen.
Medtronic Perfusion Systems is recalling DLP Pressure Monitoring Extension Line Adapters due to small pinholes in sterile packaging.
Channel Fish Processing Co. Inc. is recalling raw Oriental Breaded Fish Portions due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Cod Tails due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Haddock Cuts because the product contains undeclared milk, a major food allergen.
Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Natural Flounder Fillets due to undeclared milk, a major food allergen.
Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Pollock Squares due to undeclared milk. The product was distributed to 14 states.
Medtronic is recalling DLP Antegrade/Retrograde Adapters because small pinholes were found in a single packaging configuration of sterile pouches.
Channel Fish Processing Co. Inc. is recalling raw breaded whiting squares because the product contains milk, which is not declared on the label.
Channel Fish Processing Co. Inc. is recalling raw Oriental Breaded Fish Portions due to undeclared milk. The product was distributed to 14 states.
Medtronic Perfusion Systems is recalling DLP Pressure Disposable Pressure Display Sets because small pinholes were found in the sterile packaging.
Atrium Medical Corporation is recalling specific iCAST and Advanta V12 covered stents because the catheter hub was printed with incorrect dimensional information.
Medtronic Perfusion Systems is recalling DLP Cardioplegia Adapters with Pressure Port because small pinholes were identified in a single packaging configuration of sterile pouches.