State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
LÍLLÉbaby is recalling about 6,600 Active Series baby carriers because a sliding chest-clip strap can detach, posing a fall hazard to the child.
Wabash is recalling 2014-2019 Van trailers because limb deflectors may detach while moving, increasing crash risk. Dealers will remove the parts free of charge.
OriGen Biomedical is recalling 134 units of the VV19F Reinforced Dual Lumen Cannula because the extension tube may separate from the hub, posing a risk of blood loss.
Silver Star Brands is recalling Native Remedies VertiFree Oral Spray due to microbial contamination. Consumers should stop using the product and return it to the point of purchase.
Silver Star Brands is recalling Native Remedies EyeClear Pro Oral Spray due to microbial contamination. Consumers should stop using the product and return it to the retailer.
Silver Star Brands is recalling 53 bottles of Native Remedies VaricoGo Oral Spray due to microbial contamination. The product was distributed nationwide in the United States.
Silver Star Brands is recalling 95 bottles of Native Remedies HypoSlim Oral Spray due to microbial contamination. The product was distributed nationwide in the US.
Qualgen, LLC is recalling specific lots of Testosterone 200mg pellets nationwide due to a lack of assurance of sterility.
Qualgen, LLC is recalling Estradiol 10mg pellets nationwide due to a lack of assurance of sterility. The affected lots have specific expiration dates.
Qualgen, LLC is recalling specific lots of Testosterone 87.5mg pellets nationwide due to a lack of assurance of sterility.
Roche Diagnostics is recalling CoaguChek XS Prothrombin Time test strips nationwide because they may produce abnormally high INR results.
Ford is recalling 2019 F-250, F-350, and F-450 Super Duty trucks because an incorrect transmission casting may allow unintended vehicle movement.
Oscor, Inc. is recalling TB Series Bipolar Pacing Leads because the connector cap housing may slide, potentially exposing the connection wire and causing loss of pacing.
Zimmer Biomet is recalling 6,180 units of the RapidFlap SpinDown Clamp because the nut was assembled incorrectly. The device is used to re-attach bone flaps after craniotomy.
Ford is recalling 2018 Ford Explorer vehicles with 2.3L or 3.5L GTDI engines because a fuel pressure sensor may leak fuel, increasing fire risk.
Ford is recalling 2018 Expedition and Lincoln Navigator vehicles because missing seat brackets may allow the second-row center seat to move in a crash, increasing injury risk.
Qualgen, LLC is recalling Estradiol 15mg pellets because the company cannot ensure the products are sterile. The recall covers specific lots distributed nationwide.
Suzuki is recalling 2012-2013 SX4 vehicles because the power steering pump may seize, causing a loss of steering assist and increasing crash risk.
Qualgen, LLC is recalling Estradiol 6 mg pellets nationwide because the company cannot ensure the product is sterile.
Qualgen, LLC is recalling Estradiol 25mg pellets because the company cannot assure the sterility of the product. The recall covers specific lots distributed nationwide.
ICU Medical is recalling 5% Dextrose Injection bags because they may lack sterility and have the potential to leak.
Silver Star Brands is recalling 247 bottles of Healthful Naturals DizziFree Oral Spray due to manufacturing deviations that could result in microbial contamination.
Qualgen, LLC is recalling Estradiol 12.5mg pellets nationwide because the company cannot ensure the product is sterile.
Fred Meyer Inc. is recalling 432 units of cornbread mislabeled as Angel Food Cake Bar due to undeclared milk and soy allergens.
ICU Medical is recalling 2,580,448 bags of 0.9% Sodium Chloride Injection because they may leak and lack assurance of sterility.