State
72,971 recalls have nationwide distribution and so reach Washington. 8,456 additional recalls listed Washington specifically in their distribution scope.
Of the 8,456 recalls naming Washington we have scored against our rubric, 867 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,006 (24%) are Severe.
Which agencies issued them
These figures cover only the 8,456 recalls whose distribution notice names Washington specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Evenflo is recalling Gold Revolve360 Slim and Revolve360 Slim child seats because loose headrest foam can break off and pose a choking hazard to children.
International is recalling 2026 IC Bus CECB commercial buses because a weld on the wiper crank shaft may fail, causing the left-side wiper to stop working.
Kia is recalling certain 2021-2023 Sorento vehicles because the heating, ventilation and air conditioning blower motor wiring harness may be inadequate, which can result in a fire.
About 550 Autoez bamboo shades are recalled because long operating cords and accessible inner cords pose strangulation and entanglement hazards to children. No incidents reported.
About 28,000 RELIEVE numbing cream containers are recalled because the lidocaine product is not in child-resistant packaging as required by the Poison Prevention Packaging Act. No incidents reported.
Chrysler is recalling Mopar rear quarter glass window assemblies because the trim may not be properly secured. Detached trim can create a road hazard for other vehicles.
International Motors is recalling 2026 IC Bus CESB school buses because a weld failure may prevent the left-side wiper from working, increasing crash risk.
Land Rover is recalling certain 2023 Range Rover Evoque vehicles because water may enter the rearview camera, so the image may not appear on the display or may appear distorted.
SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCK, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 15,834 units are affected.
Unichem Cyclobenzaprine Hydrochloride Tablets, 10 mg, lot GMML24026A, are recalled because bottles labeled as cyclobenzaprine contained yellow Meloxicam 7.5 mg tablets. The FDA classified the action as Class I.
3M Ranger Blood/Fluid Warming High Flow Sets are the subject of a field action to clarify flow rates, inlet fluid temperatures and the location of the outlet temperature. The FDA classified it as Class I.
SmartDrive MX2+ SpeedControl Dials are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. The FDA classified the action as Class I. 25,389 units are affected.
SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCMC, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 8,413 units are affected.
Volkswagen is recalling one Audi SQ7 vehicle because the fasteners securing the high pressure fuel pump may not be tightened properly, resulting in a fuel leak. The vehicle has been repaired.
Volkswagen is recalling certain 2025-2026 GTI, Golf R, Audi A5, S5, A6 and Q4 e-Tron models because the torsion bar in one or both front seat belt retractors may have been damaged during production.
Sun Pharmaceutical's Kit for the Preparation of Technetium Tc 99m Mertiatide, lot AD70995, is recalled after an out-of-specification result for sulphate in the sodium tartrate dihydrate used in production. 1,870 kits are affected.
Campsite Lentejas, 4.0 oz, lot 52060, is recalled because Yellow #5 and Yellow #6 are undeclared. 154 packages are affected.
SureStep Foley Tray Systems, REF A303316A lot NGJX6399, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating, risking infection or allergic reaction.
Sand Bar, Great American and First Street branded frozen raw shrimp in 2 pound bags is recalled because it was made under insanitary conditions and may have been contaminated with Cesium-137.
Exactech Equinoxe Reverse Shoulder humeral liners in 38 mm and 42 mm sizes are recalled because the articular surface position falls outside the dimensional specification in the labeling. 11,542 units are affected.
SureStep Foley Tray Systems, REF A303414A lot NGJY3685, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating, risking infection or allergic reaction.
UniCel DxH 800 Coulter Cellular Analysis Systems configured with the LED HGB photometer are recalled because they may produce erroneously high hemoglobin results on samples with elevated white blood cell counts.
Fagron Sterile Services bevacizumab (Avastin) Injection, 1.25 mg/0.05 mL single-dose syringes, is recalled nationwide for lack of assurance of sterility. 109,320 syringes are affected.
Lippert is recalling specific paddle latches used on REV Recreation Group vehicles because they may lock unintentionally, preventing access to the liquid propane compartment and increasing fire risk.
SureStep Foley Tray Systems with Bard Lubri-Sil catheters, REF A942216 lot NGJX4320, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating. 3,670 units are affected.