State
72,940 recalls have nationwide distribution and so reach Washington. 8,456 additional recalls listed Washington specifically in their distribution scope.
Of the 8,456 recalls naming Washington we have scored against our rubric, 867 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,006 (24%) are Severe.
Which agencies issued them
These figures cover only the 8,456 recalls whose distribution notice names Washington specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Blue Bird is recalling 2025-2027 Vision school buses because a missing support brace may cause the wheelchair lift to fail, increasing injury risk.
Accriva Diagnostics is recalling 20,250 Hemochron Activated Clotting Time Low-Range test cuvettes because a foreign object with sharp edges may pose a risk of injury if not detected before handling.
Philips North America is recalling the IntelliVue Patient Monitor MX550 over a potential issue where the monitors did not alarm.
Great Lakes Cheese is recalling 1,850 cases of Good & Gather Mozzarella & Parmesan shredded cheese blend over potential metal fragments originating in a supplier raw material.
Great Lakes Cheese is recalling 235,789 cases of low-moisture part-skim mozzarella shredded cheese, sold under 26 brands, over potential metal fragments from a supplier raw material.
Water Pure is recalling 17,612 bottles of My Bladder dietary supplement because the product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303.
Paragon 28 is recalling 20 Phantom Fibula Nails because out of specification thread depths may prevent the implant from mating with its mounting bolt, potentially requiring surgery to be aborted.
Philips North America is recalling the IntelliVue MP80 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX600 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX100 over a potential issue where the monitors did not alarm.
Get Tested International AB is recalling 17 units of its DHEA Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 2 units of its Gut Microbiome Test Mega because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 13 units of its Iodine Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 7,944 containers of Dynashield 4 oz cream over current good manufacturing practice deviations.
Get Tested International AB is recalling 47 units of its Blood Type Test because the product was distributed without premarket approval or clearance.
Baxter Healthcare is recalling 118 Welch Allyn thigh replacement bladder kits because a kit may contain a Large Adult size bladder rather than a Thigh size bladder.
Blossom Pharmaceuticals is recalling 18,912 containers of Wecare Enema, 4.5 Fl Oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 4 units of its MPOX Test because the product was distributed without premarket approval or clearance.
Fresenius Kabi USA is recalling 15,862 Ivenix Infusion System large volume pumps because downstream occlusion alarms may occur at low flow rates when a check valve is added to the administration set.
Cipla Limited is recalling 4,438 cartons of Phytonadione Injectable Emulsion, USP 10mg/mL, after the product failed stability specifications with out-of-specification colour index results.
Get Tested International AB is recalling 4 units of its Continuous Glucose Monitor (CGM) because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 18 units of its Neurotransmitters Basic because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 94 units of its Parasite Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 27 units of its PSA Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 55 units of its SIBO Test because the product was distributed without premarket approval or clearance.