State
72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Heil is recalling 2020-2023 Side Loader garbage trucks because a battery support bracket may break, damaging the battery case and increasing fire risk.
Winnebago is recalling certain 2024-2025 Ekko recreational vehicles due to damaged tire valve extensions that can cause air loss in the inner tire and overload the outer tire, creating a crash risk. Dealers will replace the extensions free of charge.
Bendix is recalling specific Knorr-Bresme brake chambers for buses due to improper manufacturing that can cause air leaks and increase fire risk.
KidKraft Farm to Table play kitchens are being recalled because clothing can catch on the accessory hooks. A 23-month-old child died from strangulation and asphyxia in February 2023.
IKEA 365+ VÄRDEFULL garlic presses are being recalled because small metal pieces can detach, posing laceration and ingestion hazards. Three lacerations have been reported globally.
The Cosco 2-Step Kitchen Stepper is being recalled because the safety bar can detach or break while in use. Thirty-four reports include two incidents resulting in head injuries.
Tegu Magnetic Floating Stackers are being recalled because magnets can loosen and detach, violating the mandatory standard for toy magnets. Thirty-one reports of magnets separating have been received.
Baby Loren Morning children's cotton loungewear dresses are being recalled because they violate the flammability standards for children's sleepwear. About 340 units are affected.
Storyteller Overland is recalling 2023 Mode LT recreational vehicles because improperly tightened shore power inlets may overheat and cause a fire. Dealers will replace the inlets free of charge.
Amazon Basics Premium Foam Eurotop Mattresses are being recalled because they violate a mandatory flammability standard for mattresses. About 2,700 units are affected.
Premier Trailer Solutions is recalling 2024 Reel and Pole trailers because improperly installed oil seals may leak oil onto the brake system, reducing braking ability.
Leatherman Charge Plus and Charge Plus TTi multi-tools are being recalled because the tip of the knife blade does not fully fold into the handle, posing a laceration hazard. About 17,000 units affected.
RIDGID 18Volt Brushless 21-Degree and 30-Degree Framing Nailers are being recalled because the dual action engagement system can malfunction and involuntarily discharge a nail. About 64,000 units affected.
GE HealthCare SIGNA PET/MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Biofinity XR Toric Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 397 units are affected.
Brinkley RV is recalling certain 2025 Model Z trailers because the electrical wiring may not be secured properly, which can damage the wiring and cause a short circuit.
The Stryker StrykeFlow Disposable Suction/Irrigator with Disposable Tip is being recalled because irrigation solution may leak into the handpiece and battery pack, causing it to malfunction.
BD COR System Software version 8.80 and above is being recalled because of a potential functionality issue supporting the Over labeling feature that could lead to possible false negative results. 7 systems affected.
GE HealthCare Discovery MR750w 3.0T MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
The Medtronic CareLink SmartSync Patient Connector is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.
Endosee System Convenience Kits are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 991 units are affected.
Endosee System Convenience Kits with IV Tube are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 475 units affected.
The Azurion 7 M20 fluoroscopic x-ray system is being recalled because of the potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose. 78 units affected.
Ritz Cracker Sandwiches 20 count variety packs are being recalled because of undeclared peanut allergens due to mispackaging. 13,872 cases are affected.
Epinephrine Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL vials compounded by Imprimis NJOF are being recalled because of subpotent assay results during stability testing. 6,880 vials affected.