State
72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 11,000 3-Pack Smoke Detector Fire Alarms are being recalled because if the sensing threshold is set too high, the alarm might not sound in a timely manner.
About 550 Fortemotus-branded adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 590 CheerKid baby bath seats are being recalled because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
About 800 Beloems-branded adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
B.C. Williams Bakery Service is recalling 51 bags of Spice Cake Mix, sold in 50 lb bags, over an undeclared milk allergen.
Boston Scientific is recalling 266 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.
Green Lumber Holdings is recalling Green Lumber Natural Fuel For Men capsules because FDA analysis found the product to contain tadalafil, and it is marketed without an approved application.
B.C. Williams Bakery Service is recalling 95 bags of Swiss Chocolate Cake Mix, sold in 50 lb bags, over an undeclared milk allergen.
B.C. Williams Bakery Service is recalling 720 bags of Bread and Roll Mix, sold in 50 lb bags, over an undeclared milk allergen.
Boston Scientific is recalling 59 units of the AXIOS Stent and Electrocautery-Enhanced Delivery System, 8mm x 8mm after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 39 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 150 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 8mm x 8mm, after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 557 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 20mm x 10mm, after increased reports of stent deployment and expansion issues.
Boston Scientific is recalling 588 units of the HOT AXIOS Stent and Electrocautery-Enhanced Delivery System, 20mm x 10mm after increased reports of stent deployment and expansion issues.
Nissan is recalling certain 2023-2025 Rogue vehicles with the 1.5L VC-Turbo engine because increased temperatures can break down the engine oil, causing the bearings to seize and the engine to fail.
General Rubber is recalling specific Xcellent Roadbreaker A/T tires that may crack and separate, increasing the risk of a crash.
Nissan is recalling certain 2024-2025 Rogue vehicles with the 1.5L VC-Turbo engine because the gears in the electronic throttle body assembly may break, causing a loss of drive power.
Olympus is recalling 3,361 Single Use Electrosurgical Knife KD-645 units because deterioration of the cutting knife, including overheating and burning, can contribute to tip breakage during use.
Granules Pharmaceuticals is recalling 71,424 bottles of Trazodone Hydrochloride, USP 50 mg, over the presence of foreign tablets or capsules.
bioMerieux is recalling 2,668,954 VITEK 2 Gram-negative Susceptibility Cards over a potential risk of quality control failures and false resistant antibiotic results.
Vortex Surgical is recalling 14,789 units because there may be voids in the seal of the Tyvek pouches, which compromises the sterile barrier.
Diva Fam is recalling Sea Moss Gel Superfood in the Orange variety over potential Clostridium botulinum contamination.
Diva Fam is recalling Sea Moss Gel Superfood in the Blue Spirulina and Raspberry variety over potential Clostridium botulinum contamination.
Diva Fam is recalling Sea Moss Gel Superfood in the Soursop variety over potential Clostridium botulinum contamination.
Changchun Wancheng Bio-Electron is recalling 3,000 units of Vivoo Vaginal pH Test because tests requiring a 510(k) were distributed before they could be legally marketed.