State
73,817 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.
Of the 8,536 recalls naming Washington we have scored against our rubric, 865 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,405 (28%) are Severe.
Which agencies issued them
These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mary's Harvest Fresh Foods is recalling Whole Foods Market Vegetable Bowls with Hummus due to potential E. coli O26 contamination.
Mary's Harvest Fresh Foods is recalling Trader Joe's Asian Stir Fry packages due to potential contamination with E. coli O26.
Medtronic is recalling Deep Brain Stimulation lead kits because the depth stop may not secure properly, potentially causing the lead to be placed beyond the intended target.
Mary's Harvest Fresh Foods is recalling Safeway Stir Fry Vegetables due to potential contamination with E. coli O26. The product was distributed in Oregon and Washington.
Mary's Harvest Fresh Foods is recalling 43 cases of Vegetable Blend NSM due to potential E. coli O26 contamination. The product was distributed in Oregon and Washington.
Grandma's Herbs is recalling Cholesterol Support dietary supplements because they contain undeclared soy lecithin, a common allergen.
Mary's Harvest Fresh Foods is recalling Trader Joe's Healthy 8 Chopped Veggie Mix due to potential contamination with E. coli O26.
Handi-Craft is recalling Dr. Brown's Natural Bottle & Dish Soap because it may contain harmful bacteria. No injuries have been reported.
Mary's Harvest Fresh Foods is recalling specific broccoli and cauliflower mix products due to potential contamination with E. coli O26.
Medtronic Navigation is recalling 277 reusable ENT suction instruments because they fail pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Mary's Harvest Fresh Foods is recalling Fred Mayer Vegetable Weekender Kits due to potential E. coli O26 contamination. The product was distributed in Oregon and Washington.
Alcon is recalling 367 ORA Systems with VerifEye because a software error may cause incorrect intraocular lens power measurements during cataract surgery.
Shippert Medical Technologies is recalling Tissu-Trans Filtron 100 units because the seal integrity of the sterile packages cannot be assured.
Mary's Harvest Fresh Foods is recalling Stir Fry Vegetables Bowl packages due to potential contamination with E. coli O26.
Mary's Harvest Fresh Foods is recalling 5 lb. cases of Stir Fry Mix Legacy due to potential E. coli O26 contamination. The product was distributed in Oregon and Washington.
Mary's Harvest Fresh Foods is recalling specific vegetable snack and tray products due to potential contamination with E. coli O26.
Medtronic is recalling eight AxiEM ENT suction kits because the instruments fail mandatory pre-use verification tests.
Medtronic is recalling 15 Fusion ENT Instrument Kits because the instruments fail pre-use verification. The kits were distributed in the US and Canada.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 60 mg, due to a label mixup that may result in mislabeling.
C. O. Truxton is recalling Phenobarbital Tablets USP, 100 mg, due to a label mixup that may result in mislabeled products.
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 500 because the seal integrity of the sterile packages cannot be assured.
Medtronic is recalling 13 reusable ENT instrument sets because they fail required pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Pentax of America Inc is recalling 116 ultrasound video gastroscopes because the instructions for use contain an error in the disinfection step.
C. O. Truxton is recalling specific lots of Amitriptyline HCL 50 mg tablets due to potential label mixups. The recall is nationwide.
Medtronic is recalling 75 Curved Suction 90 ENT instruments because they fail required pre-use verification checks.