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.
Candela Corporation is recalling HFC-134a coolant canisters because the neck bushing may become loose and separate from the canister body during use.
Kawasaki is recalling about 1,100 lawn mower engines because a damaged fuel line can leak fuel, posing burn and fire risks.
Community Products is recalling 1,079 Rifton TRAM Low Base powered lift devices because a design change makes the latch springs susceptible to fatigue failure.
GE Healthcare is recalling ApexPro Telemetry Server Systems because they may fail to provide visual or audible alarms for ECG arrhythmias, lead failures, or pulse oximetry issues.
Smiths Medical ASD Inc. is recalling GRIPPER Needles because some may be occluded or blocked, posing a risk to patients.
Temp-Air is recalling 2017-2019 EBB-80 trailers because an incorrect hitch coupling may limit adjustability, potentially causing the trailer to drag and increasing crash risk.
Beckman Coulter is recalling Lipase assays because acetaminophen metabolites cause negative interference in overdose patients.
Community Products, LLC is recalling 3,282 Rifton TRAM Standard Base powered lift devices due to a design defect that may cause the latch mechanism to fail after repeated use.
Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for clinical variants.
Becton Dickinson is recalling 1.7 million BD Vacutainer Push Button Blood Collection Sets because the front and rear barrels may separate when the needle retracts.
Beckman Coulter is recalling Uric Acid assays because acetaminophen metabolites cause negative interference in overdose patients.
Siemens Healthcare Diagnostics is recalling Atellica IM 1300 Analyzers running software versions V1.19.0 and V1.19.2 due to issues scanning new reagent lot test definitions.
Community Products, LLC is recalling 167 Rifton E-Pacer powered lift devices because a design change makes the load-bearing buckle springs susceptible to fatigue failure.
The Truck Farm, LLC is recalling Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix because the product contains wheat flour but does not declare wheat on the label.
Andover Healthcare Inc. is recalling 1,798 cases of sterile Co-Flex NL 3-inch wound dressings because of incomplete packaging seals that may compromise sterility.
Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for clinical variants.
ICU Medical is recalling 47,152 Plum 360 Infusion Systems because a software malfunction can cause the device to become inoperable with a blank screen when used with a MedNet Custom Drug Library.
Siemens Healthcare Diagnostics is recalling Atellica IM 1600 Analyzers running software versions V1.19.0 and V1.19.2 due to issues scanning new reagent lot test definitions.
Candela Corporation is recalling HFC-134a coolant canisters because the neck bushing may become loose and separate from the canister body during use.
Andover Healthcare Inc. is recalling 330 cases of Sterile Co-Flex LF2 3" wound dressings because of incomplete packaging seals that may compromise sterility.
Andover Healthcare Inc. is recalling 8,500 cases of sterile Co-Flex NL 4-inch wound dressings because of incomplete packaging seals that may compromise sterility.
Ducati is recalling 2019-2020 Hypermotard 950 and 950 SP motorcycles because a broken battery terminal may cause engine stalls, increasing crash risk.
Andover Healthcare Inc. is recalling 269 cases of Sterile Co-Flex Med 3" wound dressings due to incomplete packaging seals that may compromise sterility.
Baxter Healthcare is recalling EXACTAMIX Empty EVA TPN bags because they may leak after being used for compounding sterile solutions.
Candela is recalling HFC-134a coolant canisters because the neck bushing may separate during use in specific legacy devices.