State
73,741 recalls have nationwide distribution and so reach Washington. 8,535 additional recalls listed Washington specifically in their distribution scope.
Of the 8,535 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 2,404 (28%) are Severe.
Which agencies issued them
These figures cover only the 8,535 recalls whose distribution notice names Washington specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Siemens is recalling seven AXIOM Artis BA X-ray systems because a power supply defect may cause the generator to fail, preventing X-ray imaging.
Abbott Laboratories is recalling 8,132 C3 in vitro diagnostic kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Abbott Laboratories is recalling 5,483 units of ARCHITECT BNP Calibrators worldwide due to a time-dependent stability drift that affects patient and control test results.
Pharma-Natural Inc. is recalling Army Health Pain Reliever Gel with Curcumin because it was manufactured with current good manufacturing practice violations.
Epimed International is recalling 98 Versa-Kath Mini Kits because the labeling incorrectly states the kit contains a 12-gauge catheter, while it actually contains a 21-gauge catheter.
Medela Inc is recalling 665,600 breast milk transfer lids because packaging breaches may compromise sterility, even if the packaging appears intact.
Merge Healthcare is recalling 73 units of Merge OrthoPACS software due to potential display errors in image ordering and scrolling.
Siemens is recalling five AXIOM Artis TA units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.
Siemens is recalling six AXIOM Artis BC units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.
Pharma-Natural Inc. is recalling Dermanak Skin Fade Cream because it was manufactured with current good manufacturing practice violations.
Siemens is recalling 53 AXIOM Artis dBC units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.
Siemens is recalling 98 AXIOM Artis dTC units because a power supply tolerance issue may cause generator failure, preventing X-ray imaging.
Abbott Laboratories is recalling ARCHITECT BNP Controls because of a time-dependent stability drift that affects test results.
Lupin Pharmaceuticals is recalling Nystatin and Triamcinolone Acetonide Cream due to a failed uniformity of containers test. The recall covers 33,939 tubes distributed nationwide.
Tristar Products is recalling magnetic trivets because magnets can detach and be swallowed by children, causing serious internal injuries.
Gulf Stream is recalling 2017 Serro Scotty S14 RBR travel trailers because the Federal Placard label displays an incorrect Gross Vehicle Weight Rating (GVWR).
Mazda is recalling 2019 Mazda3 vehicles with manual dimming mirrors because the mirror may detach, reducing rearward visibility and increasing crash risk.
Temsa is recalling 2014-2019 TS45 buses because hydraulic steering hoses may leak or burst, potentially affecting steering ability and increasing crash risk.
Meritor is recalling specific front steer axles that missed a heat treat step, potentially causing fractures and loss of vehicle control.
Piaggio is recalling specific Moto Guzzi and Aprilia motorcycles because a front brake master cylinder defect may cause unexpected slowing or stopping without warning to following traffic.
Chrysler is recalling 2019 Ram 1500 vehicles because the instrument cluster may fail to illuminate driver warnings, increasing crash risk. Dealers will replace the cluster free of charge.
Spansive is recalling about 950 wireless multi-phone chargers sold in May 2019 because metallic accessories can overheat, posing a burn hazard.
Forest River is recalling 2018-2019 Starcraft Allstar, Allstar XL, and Starlite vehicles because the roof hatch external handle may break, preventing emergency egress.
Cycling Sports Group is recalling 2013-2016 Cannondale CAADX bicycles because the fork can break, posing a fall hazard. One fatality and seven serious injuries have been reported.
Vantage Mobility is recalling 2012-2018 Toyota Sienna wheelchair vans because short rear brake hoses may rub against the axle, risking brake failure and loss of control.