State
73,388 recalls have nationwide distribution and so reach Washington. 8,462 additional recalls listed Washington specifically in their distribution scope.
Of the 8,462 recalls naming Washington we have scored against our rubric, 868 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,396 (28%) are Severe.
Which agencies issued them
These figures cover only the 8,462 recalls whose distribution notice names Washington specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Stryker INBONE Tibial Trays are being recalled due to an oversized lock detail that could affect proper component assembly and implant function. Affected units were distributed in New York.
Merit Medical Systems is recalling CorVocet Biopsy Systems due to manufacturing defects that may cause the needle to eject when triggered outside the body, risking needle stick injuries to users or patients.
Encore Medical is recalling EMPOWR hip liner implants because boxes may contain knee inserts instead. This packaging error could delay surgeries. Four units affected in six US states.
The Chai Box Chai Concentrate is being recalled due to potential Clostridium botulinum contamination identified during testing. Affected products have best-by dates from September 2022 to March 2023.
Medline is recalling 1,020 peripheral blood culture draw kits due to incorrect expiration dates on kit components. The CHG solution and Bactec bottle plastic have expiration dates that do not match the date listed on the kit.
Medline recalls Adult Blood Culture Collection Kits due to incorrect expiration dates on kit components. The expiration dates on the CHG Solution and Bactec bottle plastic do not match the dates listed on the kit packaging.
Medline is recalling 760 blood culture kits because the expiration dates printed on the kit do not match the expiration dates on the CHG Solution and Bactec bottle components inside.
ConvaTec is recalling 3,209 units of its Active Life One-Piece Drainable Pouch due to impaired functionality of the release liner. Contact the manufacturer with your batch number.
VistaPharm recalls 1980 unit-dose cups of pyridostigmine bromide oral solution due to a preservative ingredient found out of specification during quality control. Lot 832400, nationwide distribution.
LumiraDx is recalling 83 SARS-CoV-2 Antigen Liquid Quality Control Kits (batch 2002204017) with incorrect vial lot numbers. The kits contain Flu A/B lot numbers instead of SARS-CoV-2 Ag numbers, causing error messages and preventing device use.
Hip and knee implant boxes from Encore Medical may contain the wrong product, potentially causing surgery delays. The FDA is recalling affected units to prevent unavailability of correct implants.
Angiodynamics is recalling 11 Vortex MP Port Titanium implantable ports because printed Instructions for Use were not shipped with the devices. Missing instructions could lead to improper implantation or post-operative care.
Daimler Trucks North America is recalling certain Freightliner Cascadia and Western Star models due to corrosion in front brake modulator valves. The defect may cause brakes to pull to one side during automated braking, increasing crash risk.
Tesla is recalling 2017-2021 Model S and Model X vehicles due to power steering assist failure on rough roads or after hitting potholes, which increases crash risk.
Tesla is recalling 2021 Model S exterior rearview mirrors that do not meet federal rear-visibility standards. Defective mirrors may cause drivers to misjudge vehicle distances, raising crash risk.
Hyundai is recalling 2021-2023 Santa Fe Hybrid and 2022-2023 Santa Fe Plug-In Hybrid vehicles, plus 2023 Genesis G80 Electric vehicles, because seat belt pretensioners may explode in a crash and project metal fragments. Dealers will secure the pretensioners with a cap at no cost.
Forest River is recalling specific 2019-2022 fifth wheels because a cross-member may fail to retain holding tanks, increasing crash risk.
Volkswagen Group of America is recalling 296,044 Volkswagen and Audi vehicles (model years 2019-2021) because the tire pressure monitoring system may fail to detect simultaneous pressure loss in all four tires, increasing crash risk. Dealers will update the TPMS software at no charge.
Tiffin is recalling approximately 295 motorhomes from 2022-2023 because the LPG hose fitting connected to the regulator may leak at the swivel joint, creating a fire hazard in the presence of an ignition source.
Foster Farms is recalling approximately 148,000 pounds of frozen chicken patties sold at Costco in five states due to possible hard plastic contamination.
Micro Bird is recalling 2019-2022 G5 school buses because a faulty connection may cause sudden loss of power steering and brake assist, increasing crash risk.
Micro Bird is recalling one 2019 G5 transit bus because a faulty connection may cause power steering fluid loss, reducing brake assist and increasing crash risk.
Yokohama Off-Highway Tires America is recalling specific tires because the date code on the sidewall is incorrect, which hinders age identification.
Goalsetter is recalling about 18,000 wall-mounted basketball goals because they can detach from walls and fall. One fatality and multiple injuries have been reported.
Horizon T101-05 folding treadmills can unexpectedly accelerate, change speed, or stop without user input, posing a fall hazard. About 192,000 units sold in the U.S. are affected; 71 injuries including broken bones have been reported.