State
73,809 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.
Of the 8,536 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 2,405 (28%) are Severe.
Which agencies issued them
These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Spartan Motors is recalling 2001-2019 MetroStar and Gladiator emergency vehicles because EMS cabinet fasteners may be the wrong size, posing a crash injury risk.
Philips is recalling INTEGRIS Allura 9 F FDXD systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Philips is recalling 5,115 Allura Xper FD2O Biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Philips is recalling INTEGRIS Allura 15-12 systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Hetero Labs Limited is recalling 98,016 bottles of Montelukast Sodium 10 mg tablets because a pharmacist reported blue specks on the tablets.
Zimmer Biomet is recalling 16 Vanguard 360 Revision Knee System tibial block augments because the sterile packages contained one bolt instead of the required two.
Pin Hsiao & Associates, LLC dba Zen Bakery is recalling Trader Joe's Cinnamon Coffee Cake because it contains undeclared soy lecithin.
Baxter Healthcare is recalling 523,896 bags of Levofloxacin Injection in 5% Dextrose because the drug concentration was higher than specified.
Tosoh Bioscience Inc is recalling eight G8 Automated HPLC Analyzers because they were distributed with software that lacks a 510(k).
Confidence Inc. is recalling Bone-Lock dietary supplements containing undeclared ingredients, including Hydroxypropyl Methylcellulose, Titanium Dioxide, and Polyethylene Glycol.
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.
Zimmer Biomet is recalling 16 Vanguard 360 Revision Knee System tibial block augments because the sterile packages contained only one bolt instead of the required two.
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.
Medtronic is recalling 250 units of DxTerity TRA 5F Diagnostic Catheters because the inner pouch may incorrectly display a 6 French size indicator instead of the correct 5 French size.
Swire Coca Cola USA is recalling Caffeine-Free Barq's Root Beer 12 Packs due to mislabeling. The recall covers 2,945 cases distributed nationwide.
Entegra is recalling 2019 Aspire, Anthem, and Insignia motorhomes because the park brake may fail to hold the vehicle on a grade.
Jayco is recalling 2019 Precept and Precept Prestige motorhomes because improperly heat-treated front wheel studs may break, increasing crash risk.
AAA Innovations is recalling about 275 promotional cooler grills because the wooden cabinet can catch fire. No injuries have been reported.
Entegra is recalling 2019 Anthem, Aspire, Cornerstone, and Insignia motorhomes because improperly adjusted entry door latch rods may allow the door to open during transit.
Jayco is recalling 2019 Jay Flight travel trailers because incorrectly wired turn signal and brake lights may fail to operate, increasing crash risk.
Winnebago is recalling 2017-2019 Minnie Drop trailers because a missing clamp may allow the propane line to contact the refrigerator burner, posing a fire risk.
Mercedes-Benz is recalling certain 2016-2018 GLC models because rear seat belt latch plates may retract into the interior paneling, preventing use.
UberScientific is recalling Uber Numb topical anesthetic cream and spray because the packaging is not child-resistant, posing a risk of poisoning to young children.
Chrysler is recalling 2018-2019 Jeep Wranglers because improperly welded front track bar brackets may separate, reducing steering capability and increasing crash risk.