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.
Kimberly-Clark is recalling U by Kotex Sleek Regular Tampons because they may come apart upon removal.
Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Tray Bases because they may shed silicone during cleaning and sterilization.
Meridian Bioscience is recalling Premier Cryptococcal Antigen kits because an enzyme reagent may not maintain stability, potentially causing false negative results.
Waldemar Link is recalling 11 LINK STEM Reconstruction Prostheses because a manufacturing defect prevents the reaming guide from reaching the intended depth, which may lead to incorrect surgical positioning.
Bayer Medical Care is recalling MAVIG Portegra and Portegra2 Overhead Counterpoise Systems because the head mount knob may not be properly tightened, causing the injector head to become loose or fall.
Kimberly-Clark is recalling U by Kotex Sleek Regular Tampons because the product may come apart upon removal.
Waldemar Link is recalling 31 BiMobile UHMWPE Liners because internal labels may contain incorrect part numbers, risking errors in patient records.
Teva Pharmaceuticals USA is recalling specific lots of Olmesartan Medoxomil and Hydrochlorothiazide Tablets because they failed to meet dissolution specifications.
Waldemar Link is recalling 30 BiMobile UHMWPE Liners because internal labeling may contain incorrect part numbers, risking errors in patient records.
Arrow International Inc. is recalling specific lots of pediatric central venous catheters because the lidstock labels list incorrect priming volumes and flow rates.
Bound Tree Medical is recalling 84 Curaplex Epi Safe Administration and Training Kits because the epinephrine vials inside expired in December 2018, despite the outer label showing January 2020.
Bound Tree Medical is recalling 747 Curaplex Epi Safe Kits because they are incorrectly labeled with an expiration date of May 2018 instead of May 2019, and the syringe component lacks 510(k) clearance.
Forest River is recalling 2017-2019 Glaval Entourage and Berkshire Coach Ultra motorhomes because a block heater cable defect may cause a fire.
Mack Trucks is recalling 2018 Anthem and Pinnacle vehicles because a clutch component may fail, causing unintended movement and increasing crash risk.
Johnsonville is recalling raw ground pork patties potentially contaminated with black rubber. Consumers should discard or return the affected products.
Hino is recalling 2007-2019 NJ8J trucks because missing front brake dust shields can cause the vehicle to pull left in wet conditions, increasing crash risk.
Trail King is recalling 2016-2017 ACS and AACS trailers because the fifth wheel coupler plate may crack, potentially allowing the trailer to detach from the tractor.
Heartland is recalling 2019 Prowler and Trail Runner trailers because their Federal Certification Labels may list incorrect tire size, load range, and pressure information.
Volvo is recalling 2018-2019 XC60 vehicles because tailgate lifting arms may freeze and separate in cold temperatures, posing an injury risk.
Jaguar Land Rover is recalling 2019 Range Rover and Discovery models because a crankshaft pulley bolt may fracture, causing engine failure and increasing crash risk.
Perdue Foods is recalling approximately 68,244 pounds of SimplySmart Organics Gluten Free Chicken Nuggets due to possible wood contamination. Consumers should discard or return the product.
Heartland is recalling 2019 Prowler and Trail Runner trailers because they were equipped with incorrect tires that may fail, increasing crash risk.
Jaguar is recalling 2019 F-Pace, F-Type, and XJ vehicles because a defective crankshaft pulley bolt may fracture, causing engine failure and increasing crash risk.
Winnebago is recalling 2012-2018 ERA motorhomes because an overhead cabinet shelf may detach and fall, potentially distracting the driver or causing injury.
Sun Pharmaceutical Industries is recalling Vecuronium Bromide for Injection because glass particles were detected in the product.