State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Altec is recalling 2015-2019 AC26, AC28, AC30, and AC38 crane aerial devices because a boom lift cylinder hose may lack a velocity fuse, risking uncontrolled movement.
Flexicare Medical Ltd. is recalling BriteBlade Pro laryngoscope blades because internal components may become loose and separate, posing a risk of entering the patient's oral cavity.
Cook Inc. is recalling specific lots of Dawson-Mueller Drainage Catheters because they were not manufactured to specification, which could lead to leakage from the Mac-Loc hub assembly.
Flexicare Medical Ltd. is recalling BriteBlade Pro laryngoscope blades because internal spring, washer, and bearing components may become loose and separate from the device.
Physio-Control is recalling 29,952 LIFEPAK 15 Monitor/Defibrillators worldwide because oxidation on the keypad may prevent the device from delivering a shock.
Assurance Infusion is recalling 1,290 vials of TRIMIX injection nationwide due to a lack of sterility assurance. No specific illnesses or injuries are reported in the source text.
Bob's Red Mills is recalling specific 25 oz packages of Garbanzo Beans due to the potential presence of glyphosate. The recall affects products distributed in the US and several international locations.
McGuff Compounding Pharmacy Services is recalling Lipoic Acid Injection vials because filmy or cloudy particulate matter was observed in the product.
Microbiologics Inc is recalling 810 units of the Gram-Positive Blood Culture Control Panel because the recommended hydration fluid has changed to sterile DI water or pH 7.2 phosphate buffer.
Riverpoint Medical is recalling 3,234 sterile 18G Brachy Grids because the integrity of the sterile packaging is potentially compromised.
Columbia Bean & Produce is recalling dry garbanzo beans sold under multiple brands because 11.8 ppm of glyphosate was detected.
Caire, Inc. is recalling four European version FreeStyle Comfort Oxygen Concentrators because they were not cleared for use in the US.
Columbia Bean & Produce is recalling 13 Bean Soup Mix due to potential glyphosate contamination. The product was distributed in seven US states and Canada.
Bob's Red Mill is recalling 13 Bean Soup Mix due to the potential presence of glyphosate. The product was distributed in multiple US states and international locations.
Teleflex Medical is recalling RuSCH One piece Male External Regular Catheters because the labels incorrectly state the devices are sterile, though they are not required to be.
AuroMedics Pharma LLC is recalling Moxifloxacin Ophthalmic Solution due to market complaints of discoloration. The affected product is distributed nationwide in the U.S.
Teleflex Medical is recalling RuSCH One piece Male External Medium Catheters because the labels incorrectly state the devices are sterile, though they are not required to be.
Lupin Pharmaceuticals is recalling specific lots of Tri-Lo-Marzia oral contraceptives due to out-of-specification test results found during a retrospective review of blend uniformity data.
Lion Electric Company is recalling 2018-2020 Lion C electric school buses because a hydraulic defect can cause loss of power steering and braking.
Forest River is recalling 2014-2019 Rockport Work Trucks because the roof may detach from the front cap, creating a road hazard and increasing crash risk.
Forest River is recalling 2019-2020 Georgetown GTA34H5F motorhomes because the propane gas line may melt near the refrigerator, causing a leak and fire risk.
Arcimoto is recalling 2019 FUV motorcycles because the brake line may contact the steering main-link, potentially causing a loss of braking ability and increasing crash risk.
Arcimoto is recalling 2019 FUV motorcycles because electrical interference may cause the instrument cluster display to go blank, increasing crash risk.
Terex Advance Mixer is recalling 2020 FDC300, FD4000, FD5000GL, and FD7000B vehicles because incorrectly heat-treated axle output shafts may fracture, causing loss of drive and increasing crash risk.
Toyota is recalling specific 2011-2019 Corolla, Matrix, Avalon, and Avalon Hybrid vehicles because the air bag control unit may malfunction, potentially preventing air bags and seat belt pretensioners from deploying in a crash.