State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Triumph is recalling aftermarket Quickshifter Kits for Speed Triple S motorcycles because the assembly may interfere with gear changes, increasing crash risk.
Newmar is recalling 2020 Mountain Aire motorhomes because low beam bulbs may fail to illuminate when high beams are activated, increasing crash risk.
General Motors is recalling specific 2019-2020 Chevrolet Silverado and GMC Sierra trucks because hot gas from seat belt pretensioners could ignite the carpet, causing a vehicle fire.
Chrysler is recalling Mopar steering assemblies for Ram 1500 trucks because a contaminated circuit card may short circuit, causing intermittent loss of power steering assist.
Ioxus Corporation is recalling 12V uSTART MD battery support modules because internal short circuits can cause vehicle fires.
Chrysler is recalling 2011-2013 Jeep Grand Cherokee and Dodge Durango vehicles because a fuel pump relay may fail, causing the vehicle to stall without warning and increasing crash risk.
Chrysler is recalling 2019 Ram 1500 trucks because a contaminated electric power steering gear may short circuit, causing intermittent loss of steering assist.
Briggs & Stratton is recalling about 1,160 Snapper rear engine riding mowers because a faulty lever can keep the blade engaged, posing an injury risk.
CPSC recalls Kenmore Elite microwave ovens sold at Sears due to incorrect wiring that causes the exterior to overheat, posing a burn risk.
Quest Products is recalling ALOCANE Emergency Burn Pads because the packaging is not child-resistant, posing a risk of lidocaine poisoning to young children.
Jumbo Foods is recalling Tuscan Sun brand Wedge Chicken Salad sandwiches due to potential Listeria monocytogenes contamination. The product was distributed to stores in eight states.
Jumbo Foods is recalling Tuscan Sun Cranberry Chicken Salad sandwiches due to potential Listeria monocytogenes contamination. Affected products were distributed in eight states.
Baxter is recalling Prismaflex Control Units with software below version 7.21 due to communication errors that may interrupt therapy or cause blood loss.
Baxter is recalling Prismaflex Control Units with software below version 7.21 due to communication errors that may interrupt therapy or cause blood loss.
Philips Medical Systems is recalling 1,167 Forte Gamma Camera Systems because a detector may fall vertically to the end stops of its travel limit.
Red Mountain Compounding Pharmacy is recalling S-TEST CYP 125mg/ml vials due to a lack of assurance of sterility.
Medtech SAS is recalling 93 Rosa Brain 3.0 neurosurgical devices because the instrument holder may send tools on incorrect trajectories, potentially leading to improper device placement.
Red Mountain Compounding Pharmacy is recalling specific lots of S-Lidocaine HCL 2% Injection because the product lacks assurance of sterility.
Baxter Healthcare is recalling Prismaflex Control Units with software versions below 7.21 because communication error alarms may interrupt therapy or cause blood loss.
Red Mountain Compounding Pharmacy is recalling S-Estradiol Valerate 20mg/mL injection vials because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-DMSO 100% sterile solution vials due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific vials of Magnesium Sulfate Injection because the FDA determined there is a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-E2/TEST CYP 0.4MG/1MG/MLMDV IN OIL INJECTION vials due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific lots of zinc sulfate solution because the FDA could not ensure the product was sterile.
Red Mountain Compounding Pharmacy is recalling benzalkonium chloride solution because the product lacks assurance of sterility.