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.
Griffith Labs U.S.A. is recalling 50-pound bags of Romano Garlic Seasoning due to potential Salmonella contamination from a recalled whey ingredient.
West-Ward Columbus Inc is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications.
Stryker Neurovascular is recalling FlowGate2 Balloon Guide Catheters because the balloon diameter may exceed specifications, potentially causing resistance during use.
GE Healthcare is recalling 42 Discovery RT CT systems nationwide due to a potential wiring defect in the electrical panel that may affect the uninterruptible power supply.
Hetero Labs is recalling 18,288 bottles of Indomethacin 50 mg capsules due to customer complaints of deformed, clumped, or stuck together capsules.
bioMerieux, Inc. is recalling VIDAS LH test kits because internal tests confirmed a decrease in strip signal over time, leading to invalid calibration results.
Holmquist Hazelnut Orchards is recalling Ranch Flavored Hazelnuts in 4 oz, 6 oz, and 1 lb sizes due to an undeclared hazelnut allergen in the product's 'Contains' statement.
Major Pharmaceuticals is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications.
Sugar Foods Corporation is recalling Old Chicago Basil Pesto Croutons because the whey powder used in their production was subject to a recall.
PepsiCo is recalling Diet Pepsi 7.5 oz 6-packs in five western states because the product contains undeclared aspartame.
Natus Neurology is recalling 171 Nicolet Ambulatory EEG devices because they may allow users to import exams that were not started.
Renaissance Lakewood, LLC is recalling 12,088 bags of Fluconazole Injection because the lots are out of specification for elevated sodium chloride and fluconazole assay levels.
LivaNova is recalling 243 VNS Therapy Programming Systems because they may display unintended warning messages. The devices were distributed to 16 U.S. states.
Sugar Foods Corporation is recalling Zesty Italian Croutons because they were produced using recalled whey powder. The affected product was distributed in six states.
Encore Medical is recalling 30 instrument trays used for AltiVate Small Shell Trials because a black coating may appear after cleaning that is not biocompatible.
Sugar Foods Corporation is recalling Fresh Gourmet Cubed Seasoned Croutons because they were made with recalled whey powder.
West-Ward Columbus Inc. is recalling Doxycycline Hyclate 100 mg tablets because they failed dissolution specifications.
Renaissance Lakewood, LLC is recalling 3,000 bags of Fluconazole Injection due to elevated sodium chloride and water vapor levels.
Renaissance Lakewood, LLC is recalling Fluconazole Injection bags due to elevated water vapor levels. The recall covers 3,664 bags distributed nationwide and in Puerto Rico.
Terex is recalling 2015-2018 C4000, C5000, C6000, and General 80 digger derricks because undersized welds may cause the auger to fall unexpectedly, posing an injury risk.
BYD is recalling 2016-2017 K11 M hybrid buses because a brake caliper guide pin may break, potentially causing loss of braking ability or tire pressure.
NEMO Equipment is recalling about 7,500 Stargaze recliner chairs because plastic joint supports can break, posing a fall hazard.
Micro Bird is recalling 2015-2018 G5, MB II, and T-Series transit buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in crashes.
Garden State Bus Group is recalling 2015 Double Deck Buses because the roof emergency exit is incorrectly located, potentially delaying evacuation during an emergency.
Hale Products Inc is recalling Kubota Diesel Powered Portable Pumps because improper wiring may prevent warning lamps from illuminating, increasing the risk of injury if the engine fails.