State
73,741 recalls have nationwide distribution and so reach Washington. 8,535 additional recalls listed Washington specifically in their distribution scope.
Of the 8,535 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 2,404 (28%) are Severe.
Which agencies issued them
These figures cover only the 8,535 recalls whose distribution notice names Washington specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Thor Motor Coach is recalling 2019-2020 Omni and Magnitude motorhomes because missing seat recliner parts may reduce occupant restraint in a crash.
Mercedes-Benz is recalling 24,226 vehicles due to a software fault that may cause the emergency call system to relay inaccurate location data, potentially delaying emergency responders.
Mercedes-Benz is recalling 29,720 vehicles because front seat belts may be incorrectly detected as unfastened, potentially disabling safety features.
Mazda is recalling specific 2007-2012 CX-7, CX-9, and 2009-2012 Mazda6 vehicles because the front passenger air bag inflators may explode, posing a risk of serious injury or death.
Gulf Stream is recalling 2020 Amerilite, Conquest, Innsbruck, Grand River, Kingsport, and Trail Master trailers because the gas refrigerator may not be properly sealed, potentially releasing carbon monoxide or flammable LP gases.
Honda is recalling 2019-2020 Pilot and 2019 Passport vehicles because front frame members may not be fully welded, potentially reducing crash protection.
Mazda is recalling specific 2003-2008 models because front passenger air bag inflators may explode, posing a risk of serious injury or death.
John Deere is recalling 4044R, 4052R, and 4066R compact utility tractors because improperly torqued front cab support bolts can fail during a rollover, posing a crushing injury hazard.
New Port Sales is recalling All-Gloo Craft Glue because the packaging does not meet child-resistant closure requirements, posing a poisoning hazard to children.
Roland Foods is recalling specific jars of Black Caviar due to potential Clostridium botulinum contamination. Consumers should check their pantries for the listed UPCs and batch codes.
Roland Foods is recalling specific jars of Red Caviar due to potential Clostridium botulinum contamination. Consumers should check their pantries for the listed UPCs and batch codes.
Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for clinical variants.
Avella of Deer Valley, Inc. is recalling 808 droptainers of Povidone Iodine, 5% Ophthalmic Solution due to a lack of sterility assurance.
Altec Industries is recalling 2018-2019 aerial devices that were not stability tested according to ANSI A92.2 standards, posing a risk of collapse.
Nephron Pharmaceuticals is recalling 162 bags of Amino Acid Injection due to lack of sterility assurance and potential leaks.
Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for specific clinical variants.
Nephron Pharmaceuticals is recalling 1,047 bags of del Nido Cardioplegia Solution because the bags may leak, compromising sterility.
Nephron Pharmaceuticals is recalling 1,855 bags of Fentanyl Citrate and Bupivacaine HCl injection due to potential glass contamination.
Exactech, Inc. is recalling 158 Ergo 3.2mm K-wires because they may fracture at the threads and remain in the glenoid during shoulder surgery.
Nephron Pharmaceuticals is recalling 1,370 bags of Fentanyl Citrate and Bupivacaine HCl injection due to potential glass contamination.
Euphoria Fancy Food Inc. is recalling Capitan K Salmon slightly salted pieces due to potential Listeria monocytogenes contamination. The product was distributed in New York, Pennsylvania, New Jersey, and Washington.
Nephron Pharmaceuticals is recalling 615 bags of Fentanyl and Ropivacaine Injection due to potential glass contamination from GMP deviations.
GN Otometrics is recalling 3,071 ICS CHARTR EP 200 units because undergrounded electrical surfaces may cause electrical shock to patients or healthcare professionals.
Candela Corporation is recalling HFC-134a coolant canisters because the neck bushing may separate during use in specific legacy devices.
Andover Healthcare Inc. is recalling 1,759 cases of sterile Co-Flex LF2 wound dressings because of incomplete packaging seals, which may compromise sterility.