State
72,820 recalls have nationwide distribution and so reach Washington. 8,454 additional recalls listed Washington specifically in their distribution scope.
Of the 8,454 recalls naming Washington we have scored against our rubric, 866 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,005 (24%) are Severe.
Which agencies issued them
These figures cover only the 8,454 recalls whose distribution notice names Washington specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Strawberry Fruit Bars because they may contain glass pieces.
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.
Accord Healthcare is voluntarily recalling Levothyroxine Sodium 300 mcg tablets because they may contain less active ingredient than labeled.
Church & Dwight is recalling Zicam Cold Remedy Nasal Swabs because FDA inspections found out-of-limit microbiological testing results at the contract manufacturer.
Medline is recalling 974 neurosurgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Toyota is recalling 8,521 2026 C-HR battery electric vehicles because a software error may cause the battery to overcharge, potentially leading to a loss of drive power and increased crash risk.
Midmark is recalling Digital ECG HD+12 and HD+15 units with specific IQecg plugin software versions due to a communication anomaly that may cause incorrect ECG waveforms and inaccurate heart rate calculations.
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.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.
Medline is recalling 246 surgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Healthmark is recalling ProChek protein tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 125 mcg tablets because they are subpotent. The recall is ongoing nationwide.
Fresenius Medical Care is recalling 1,140 BlueStar Hemodialysis machines due to reported flow, water, or temperature-related alarms.
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.
Medline Industries is recalling 15 convenience kits (SKU CDS980375M) due to a potentially contaminated component. The kits were distributed in 18 US states.
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 75 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.
Medline Industries is recalling 169 surgical convenience kits nationwide because they contain 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.
Healthmark Industries is recalling ProChek-II tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Medline Industries is recalling 419 surgical convenience kits because they contain a potentially contaminated component. The kits were distributed nationwide.
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.
Merge Healthcare is recalling 20 Merge PACS and Merge OrthoPACS workstations because a software issue may cause measurements to be displayed inaccurately.
Philips is recalling Incisive CT scanners with specific software versions due to a potential failure to trigger clinical scans during bolus tracking.