State
73,376 recalls have nationwide distribution and so reach Washington. 8,462 additional recalls listed Washington specifically in their distribution scope.
Of the 8,462 recalls naming Washington we have scored against our rubric, 868 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,396 (28%) are Severe.
Which agencies issued them
These figures cover only the 8,462 recalls whose distribution notice names Washington specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Textron Specialized Vehicles is recalling about 3,800 Arctic Cat Alterra 600 and Tracker 600 all-terrain vehicles because the A-arm can separate from the frame, causing loss of steering control and crash risk.
Spartan Fire is recalling 2022-2024 Gladiator, Metro Star, FC-94, and KME Panther firetrucks because the transmission may fail to engage the water pump after reversing.
Autocar is recalling 2020-2022 Xpeditor vehicles whose external fuse box may short circuit from water intrusion, causing unexpected stall and increasing crash risk. Dealers will mount the box vertically and install a protective shield.
Burnham Commercial is recalling about 185 commercial natural gas boilers because delayed ignition and flame rollout can occur, posing a burn hazard. Two flame rollouts have been reported, but no injuries.
Avanos Medical recalls BALLARD ACCESS Closed Suction System units due to manifold cracking, which can cause respiratory circuit leaks and inadequate ventilation in neonatal and pediatric patients.
Audi is recalling 2022-2023 Q4 E-Tron vehicles because the head curtain air bag may tear during deployment, increasing injury risk.
Mead Johnson & Company is voluntarily recalling ProSobee Simply Plant-Based Infant Formula due to a remote possibility of cross-contamination with Cronobacter sakazakii. Affected batches were distributed across 40+ US states and territories, Puerto Rico, Thailand, and Guam.
Avanos Medical is recalling 780 units of the BALLARD ACCESS Closed Suction System due to manifold cracking that can leak the respiratory circuit, potentially causing inadequate ventilation in neonatal and pediatric patients.
Breckenridge Pharmaceuticals is recalling Alprazolam 2 mg tablets nationwide due to manufacturing practice deviations creating potential cross-contamination risk. Affected tablets are distributed in 100-count and 500-count bottles.
Becton Dickinson recalls 1.9 million BD Insulin Syringes due to a nonsterility defect that could expose patients to pathogenic microorganisms and local infection risk.
Synthes (USA) Products LLC is recalling TFN-Advanced Femoral Nails because labeled measurements do not match actual dimensions. Nails labeled 200mm may be 170mm and vice versa.
Becton Dickinson is recalling approximately 1.1 million BD Ultra-Fine Insulin Syringes due to nonsterility concerns. The affected syringes may expose patients to pathogenic microorganisms and risk of local infection.
Pingo hot chocolate pods may contain undeclared peanut residue. Consumers with peanut allergies should not consume affected products.
Fenwal Inc is recalling certain batches of the Amicus MNC Apheresis Kit due to a potential for centrifuge packs to develop stress leaks. Affected units were distributed nationwide and internationally.
Becton Dickinson recalled 1,472,400 BD Ultra-Fine II insulin syringes due to a sterility defect. The nonsterile syringes pose a risk of local infection at injection sites.
Breckenridge Pharmaceutical is recalling multiple lots of Alprazolam 0.5mg tablets nationwide due to manufacturing process deviations that created a potential cross-contamination risk.
Two Rivers Coffee is recalling Brooklyn Bean Peanut Butter Cup Hot Cocoa pods because they may contain undeclared peanut residue. Consumers with peanut allergies should not use affected pods.
Breckenridge Pharmaceutical is recalling Alprazolam 1 mg tablets distributed nationwide due to manufacturing practice deviations that pose a potential cross-contamination risk.
Navada Imports is recalling sunflower lecithin liquid in bulk totes due to undeclared peanut allergen. The affected products were distributed nationwide to food manufacturers.
Breckenridge Pharmaceuticals is recalling Alprazolam Tablets, USP 0.25mg distributed nationwide due to a potential cross-contamination risk from manufacturing deviations.
Becton Dickinson is recalling 686,500 units of BD insulin syringes due to a nonsterile condition that may expose patients to pathogenic microorganisms and risk of infection.
Synthes TFN-Advanced Femoral Nails labeled as 200mm may measure 170mm, and vice versa. Healthcare providers should verify actual dimensions before surgical use.
Teva Pharmaceuticals is recalling 715,632 bottles of Clear Eyes Once Daily eye drops due to an out-of-specification impurity found during stability testing.
Becton Dickinson is recalling BD Ultra-Fine Insulin Syringes (Catalog Number 326719) due to a nonsterile condition that could expose patients to pathogenic microorganisms and local infection. Approximately 80,500 units distributed worldwide are affected.
Maquet Cardiovascular is recalling one Fusion Bioline Vascular Graft from lot 25162546 that failed straightness testing. The graft could reduce blood flow or cause tension, potentially leading to bleeding and pseudo-aneurysm.