State
72,940 recalls have nationwide distribution and so reach Virginia. 9,479 additional recalls listed Virginia specifically in their distribution scope.
Of the 9,479 recalls naming Virginia we have scored against our rubric, 1,285 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,294 (24%) are Severe.
Which agencies issued them
These figures cover only the 9,479 recalls whose distribution notice names Virginia specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Philips North America is recalling the IntelliVue Patient Monitor MX800 over a potential issue where the monitors did not alarm.
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 Multi Measurement Server X2 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.
Philips North America is recalling the IntelliVue Patient Monitor MX400 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP2 over a potential issue where the monitors did not alarm.
Blue Bird is recalling 2025-2027 Vision school buses because a missing support brace may cause the wheelchair lift to fail, increasing injury risk.
Enterix is recalling 201,426 InSure ONE Fecal Immunochemical Test kits after the test failed sensitivity testing with one test card lot, which may result in false negative results.
Philips North America is recalling the IntelliVue MP40 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP60 over a potential issue where the monitors did not alarm.
Breckenridge Pharmaceutical is recalling 3,397 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Philips North America is recalling the IntelliVue Patient Monitor MX700 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX450 over a potential issue where the monitors did not alarm.
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.
Ventura Foods is recalling 3,556 cases of salad dressings sold under several brands after foreign objects, described as black plastic planting material, were found in granulated onion.
Great Lakes Cheese is recalling 117 cases of Food Club Finely Shredded Pizza Style Four 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.
Illumina is recalling 11,916 NextSeq 550Dx reagent kits because flow cell gaskets have a quality issue that may cause leaks during runs, including possible toxic substance exposure to the user.
Costco is recalling 142,532 retail units of Kirkland Signature Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Costco is recalling 612 retail units of Kirkland Signature Chicken Sandwich with Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Philips North America is recalling the IntelliVue MP50 over a potential issue where the monitors did not alarm.
Get Tested International AB is recalling 10 units of its Vitamin D2 and D3 Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 6 units of its Food Intolerance Test Large because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 4 units of its MPOX Test because the product was distributed without premarket approval or clearance.