State
72,820 recalls have nationwide distribution and so reach Virginia. 9,476 additional recalls listed Virginia specifically in their distribution scope.
Of the 9,476 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 2,291 (24%) are Severe.
Which agencies issued them
These figures cover only the 9,476 recalls whose distribution notice names Virginia specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 200 mcg tablets because they are subpotent. The recall covers distribution nationwide in the United States.
Medline is recalling 974 neurosurgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
AVID Medical is recalling 45 Halyard DAVINCI TRUCUSTOM Foley catheter kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Medline Industries is recalling 2,262 medical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Medline Industries is recalling 106 C-section convenience kits distributed nationwide due to potentially contaminated components.
Canon Medical System, USA, INC. is recalling 10 Alphenix digital radiography systems because fixing screws in the ceiling suspended arm may become loose.
Medline is recalling 24 convenience kits labeled as MAJOR HEAD AND NECK PPS because they contain a potentially contaminated component.
Byron White Formulas is recalling its A-P Herbal Supplement because the label fails to declare walnuts in English, posing a risk to individuals with nut allergies.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 75 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.
Byron White Formulas is recalling A-L Complex Herbal Supplement because the label does not declare walnuts in English, posing a risk to individuals with nut allergies.
Byron White Formulas is recalling its A-FNG Herbal Supplement because the label fails to declare walnuts in English, posing a risk to consumers with nut allergies.
Medline Industries is recalling 169 surgical convenience kits nationwide because they contain potentially contaminated components.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 112 mcg tablets because they are subpotent. The recall covers nationwide distribution.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.
Medline Industries is recalling 419 surgical convenience kits because they contain a potentially contaminated component. The kits were distributed nationwide.
Fresenius Medical Care is recalling 1,140 BlueStar Hemodialysis machines due to reported flow, water, or temperature-related alarms.
Medline Industries is recalling 71 FEMORAL PACK and FEVAR convenience kits because they contain a potentially contaminated component.
Midmark is recalling IQecg Digital ECG software due to a communication anomaly that may cause incorrect waveforms and inaccurate heart rate calculations.
Lidl US Trading is recalling Eridanous Greek Style Shortbread Cookies because the labels contain only foreign languages and fail to declare wheat, soy, milk, eggs, and coconut.
Accord Healthcare is recalling specific lots of Levothyroxine Sodium 137 mcg tablets because they may contain less than the labeled amount of active ingredient.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 125 mcg tablets because they are subpotent. The recall is ongoing nationwide.
Medline is recalling 246 surgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Merge Healthcare is recalling 20 Merge PACS and Merge OrthoPACS workstations because a software issue may cause measurements to be displayed inaccurately.
IMRIS Imaging Inc is recalling 13 ORT300 operating room tables because a mechanical failure could cause unintended rotational movement, posing a risk of injury to patients.
Medline is recalling 3,468 neurosurgical convenience kits containing Pilling Wecksorb Neurosponges due to potential out-of-specification endotoxin levels.