State

Washington product recalls

73,817 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total: 8,536
Critical: 865
Severe: 2,405
Most recent: 2026-11-04

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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42426–42450 of 82353

ModerateFDA (Devices)·Z-2054-2018·2018-06-13
Siemens ADVIA Centaur TSH3-Ultra Assay Recalled for Analyzer Compatibility Issues
Siemens is recalling specific lots of ADVIA Centaur TSH3-Ultra assays because they may cause reduced dilution recovery or inoperability when used with Multi-Diluent 15 on certain analyzers.
Product
ADVIA Centaur TSH3-Ultra (Thyroid Stimulating Hormone 3 Ultra), Catalog Numbers: 06491072 (100 tests), 06491080 (500 tests), 04862625 (2500 tests)
Category
Medical Device
Distribution
28 states
ModerateFDA (Devices)·Z-2107-2018·2018-06-13
MicroAire SmartRelease Endoscopic System Recalled for Incorrect Sterilization Instructions
MicroAire is recalling SmartRelease Endoscopic Systems because the Instructions for Use contain incorrect sterilization parameters.
Product
MicroAire SmartRelease Endoscopic System, Endoscopic Carpal Tunnel Release, SmartRelease Handpiece, containing IFU rev. D The MicroAire Carpal Tunnel Release System is for use in patients diagnosed with carpal tunnel syndrome that is not associated with, or secondary to, any…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2112-2018·2018-06-13
Baxter SIGMA Spectrum Infusion Pump Recall for Instructional Mismatch
Baxter is recalling SIGMA Spectrum Infusion Pumps because the instructions for use specify a 20-inch bag drop, but the firm supplies 12.5-inch hangers.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), infusion pump, 35700BAX and 35700ABB Product Usage: The Baxter SIGMA Spectrum Infusion Pump with Master Drug Library is intended to be used for the controlled administration of fluids. These fluids may…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2080-2018·2018-06-13
Tosoh ST-AIA PACK FT3 Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK FT3 assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate thyroid results.
Product
ST-AIA PACK FT3; Part Number: 025286 Assay, Thyroid
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2061-2018·2018-06-13
NordicNeuroLab Recalls nordicICE Software Due to Coregistration Visualization Error
NordicNeuroLab AS is recalling 121 licenses of nordicICE v 2.3.14 because a software bug causes BOLD activation maps to be visualized without accounting for coregistration.
Product
nordicICE v 2.3.14 nordicICE is an image processing software package to be used by trained professionals including but not limited to physicians and medical technicians. The software runs on a standard off-the-shelf PC workstation and can be used to perform image viewing…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2115-2018·2018-06-13
Invivo Xper Flex Cardio Physiomonitoring System Recalled for Software Defect
Invivo Corporation is recalling Xper Flex Cardio Physiomonitoring Systems because users may inadvertently close the Full Disclosure Control Window using the ESC key.
Product
Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to facilitate invasive investigation of heart and vascular, disease when non-invasive indicators warrant such. The Xper Flex Cardio physiomonitoring system may be used to display…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2091-2018·2018-06-13
Tosoh ST-AIA PACK Prog II Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK Prog II assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK Prog II; Part Number: 025239 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2052-2018·2018-06-13
Hobbs Bronchial Cytology Brushes Recalled for Unauthorized Marketing
Hobbs Medical is recalling 1,820 bronchial cytology brushes because they were marketed for uses outside their FDA clearance.
Product
Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained personnel through a flexible endoscope when brush cell samples are required for cytological analysis.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2068-2018·2018-06-13
Tosoh ST-AIA Prostate Assay Recalled Due to Strensiq Interference
Tosoh Bioscience is recalling ST-AIA Prostate Assay kits because the drug Strensiq can cause inaccurate test results.
Product
ST-AIA PACK PAP; Part Number: 025262 Assay, Prostate
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2079-2018·2018-06-13
Tosoh ST-AIA PACK T4 Thyroid Assay Recalled Due to Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK T4 thyroid assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK T4; Part Number: 025258 Assay, Thyroid
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0865-2018·2018-06-13
Pharmaceutical Associates Recalls Nystatin Oral Suspension Due to Resuspension Issues
Pharmaceutical Associates Inc. is recalling Nystatin Oral Suspension because the product failed to meet specifications for appearance and resuspendability.
Product
NYSTATIN — NYSTATIN (NYSTATIN)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V394000·2018-06-12
New Flyer Transit Buses Recalled for Brake Caliper Guide Pin Defect
New Flyer is recalling 908 urban transit buses from 2014-2017 because a brake caliper guide pin may break, reducing braking ability and increasing crash risk.
Product
NEW FLYER — NEW FLYER XN60, XDE60, XD60, XT60
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V392000·2018-06-12
Ford Recalls 2018 Expedition, F-150, and Navigator for Fuel Pump Defect
Ford is recalling 2018 Expedition, F-150, and Lincoln Navigator vehicles because a fuel pump weld can fracture, causing a leak that increases fire risk.
Product
LINCOLN — LINCOLN, FORD NAVIGATOR, EXPEDITION, F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V391000·2018-06-12
Lamborghini Recalls Aventador Models Due to Engine Stall Risk
Lamborghini is recalling 2012-2018 Aventador vehicles because the engine may stall unexpectedly, increasing crash risk. Dealers will install updated software.
Product
LAMBORGHINI — LAMBORGHINI AVENTADOR
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18747·2018-06-12
Ashley Furniture Recalls Amnon Floor Lamps Due to Burn Hazard
Ashley Furniture is recalling Amnon floor lamps because the incorrect wattage label allows users to install bulbs that can melt the power switch, posing a burn hazard.
Product
Amnon floor lamps
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·18174·2018-06-12
A&I Recalls Tractor Canopies Due To ROPS Failure Injury Hazard
A&I is recalling about 6,200 tractor canopies in the U.S. and 265 in Canada because they may fail to protect operators in a rollover accident.
Product
A&I tractor canopies
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·18176·2018-06-12
Uttermost Recalls Mirrors and Wall Decor Due to Falling Hazard
Uttermost is recalling about 17,000 mirrors and wall decor items because the hanging hardware can break, causing items to fall and injure bystanders.
Product
Mirrors, art and wall decor
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·18177·2018-06-12
Lorex Recalls Three Video Monitor Models Due to Battery Burn Hazard
Lorex is recalling three video monitor models because the batteries can overheat and swell, posing a burn hazard. Consumers should stop using the monitors and contact Lorex for a refund.
Product
Lorex video monitors models LW2751, LW2752 and LW2962H
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V393000·2018-06-12
KME Predator Aerial Vehicles Recalled for Tether Control Software Defect
Kovatch Mobile Equipment is recalling 2015-2018 KME Predator Aerial emergency vehicles because the aerial platform may continue moving if the tether control is unplugged.
Product
KME — KME PREDATOR SS AERIAL, PREDATOR AERIAL
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18175·2018-06-12
Ketra Recalls D3 Recessed Downlights Due to Electrical Shock Hazard
Ketra is recalling about 3,400 D3 recessed downlights because incorrect wiring in the power supply connectors poses an electrical shock hazard. No injuries have been reported.
Product
Ketra D3 recessed downlights
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·18V390000·2018-06-11
Ford Recalls 2017-2018 Edge and 2017 Lincoln MKZ for Torque Converter Defect
Ford is recalling 2017-2018 Edge and 2017 Lincoln MKZ vehicles because inadequate welding on the torque converter may cause the vehicle to lose the ability to move, increasing crash risk.
Product
FORD — FORD, LINCOLN EDGE, MKZ
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V389000·2018-06-11
Ford Recalls 2018 F-650 and F-750 Trucks for Brake Hose Defect
Ford is recalling 2018 F-650 and F-750 trucks because brake hose fittings may lack anti-corrosion plating, risking fluid leaks and reduced braking.
Product
FORD — FORD F-750 SD, F-650 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V428000·2018-06-11
BMW Recalls 2000-2006 Models for Passenger Air Bag Inflator Rupture Risk
BMW is recalling specific 2000-2006 models because the passenger air bag inflator may rupture during deployment, potentially sending metal fragments into the cabin.
Product
BMW — BMW 325XI, M3, 330XI, 330I
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V386000·2018-06-08
Forest River Recalls 2019 Salem and Wildwood Trailers for Axle Defect
Forest River is recalling 2019 Salem and Wildwood recreational trailers because an axle equalizer defect could cause axle failure and increase crash risk.
Product
FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V385000·2018-06-08
Thor Motor Coach Recalls 2019 Motorhomes Due to Rear Axle Bolt Issue
Thor Motor Coach is recalling 691 specific 2019 motorhome models because rear axle U-bolts may be insufficiently tightened, posing a risk of axle separation and loss of control.
Product
THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, OUTLAW, FOUR WINDS, VEGAS
Category
Vehicle
Distribution
Distributed nationwide