State

Washington product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40176–40200 of 82345

SevereFDA (Devices)·Z-0198-2019·2018-10-31
Bovie J-Plasma Precise 360 Handpiece Recalled for Tip Separation Risk
Bovie Medical Corporation is recalling J-Plasma Precise 360 handpieces because the PEEK tip may separate and remain in patient tissue.
Product
J-Plasma Precise 360, single use, disposable. The Bovie J-Plasma Precise 360 Handpiece is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparascopic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0091-2019·2018-10-31
Westlab Pharmacy Recalls Cyclosporine Eye Drops Due to Process Control Issues
Westlab Pharmacy is recalling Cyclosporine 1% Human Eye Drops due to a lack of process controls. The recall covers nationwide distribution.
Product
Cyclosporine 1% Human Eye Drops, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-2776-92
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V769000·2018-10-31
Suzuki Recalls 2010-2013 Kizashi Vehicles for Fuel Tank Fire Risk
Suzuki is recalling 2010-2013 Kizashi vehicles because dust in the vent line may crack the fuel tank, increasing the risk of a fuel leak and fire.
Product
SUZUKI — SUZUKI KIZASHI
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0186-2019·2018-10-31
Alcon Recalls CyPass Micro-Stent Implant Due to Endothelial Cell Loss
Alcon is recalling the CyPass Micro-Stent implant because long-term study data showed statistically significant endothelial cell loss in patients.
Product
CyPass System 241, Intraocular Pressure Lowering Implant, CYPASS MICRO-STENT, CYPASS APPLIER, REF: 8065754001. For ophthalmic use.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0095-2019·2018-10-31
Pfizer Recalls Meropenem Injection Due to Loss of Sterility Assurance
Pfizer is recalling 71,075 vials of Meropenem for Injection because the containers may have lost integrity, compromising sterility.
Product
Meropenem for Injection, USA (I.V.), 1 gram/vial, 25 vials per carton, Sterile, Rx Only, Manufactured for: Hospira, Inc., Lake Forest, IL 60045, USA. NDC carton: 0409-3506-01; NDC vial: 0409-3506-11
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0185-2019·2018-10-31
Alcon Recalls CyPass Micro-Stent Due to Endothelial Cell Loss
Alcon Research is recalling CyPass Micro-Stent devices because long-term study data showed statistically significant endothelial cell loss in patients.
Product
CyPass System 241-S, CYPASS MICRO-STENT, CYPASS LOADED, CYPASS APPLIER, REF CATALOG #: 8065754003 For ophthalmic use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0214-2019·2018-10-31
Siemens APTIO Rack Output Module Recall for Missing Warning Label
Siemens Healthcare Diagnostics is recalling 441 APTIO Rack Output Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
APTIO RACK OUTPUT MODULE
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0276-2019·2018-10-31
Medtronic O-arm 1000 2nd Edition Imaging System Software Recall
Medtronic is recalling O-arm 1000 2nd Edition Imaging Systems due to software anomalies affecting startup, communication, and image acquisition.
Product
O-arm 1000 2nd Edition Imaging System, BASE BASE OARM Bl70000027120R SYSTEM 120V RWK, Model Number Bl70000027120R Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician…
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0205-2019·2018-10-31
ESAOTE MyLab Gamma Ultrasound System Recalled for Probe Overheating Risk
ESAOTE S.P.A. is recalling 10 MyLab Gamma, Model 7410 ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.
Product
MyLab Gamma, Model 7410
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V767000·2018-10-31
Keystone Recalls 2019 Crossroads Cruiser Trailers Due to Gas Leak Risk
Keystone RV Company is recalling 2019 Crossroads Cruiser recreational trailers because the water heater exhaust may allow carbon monoxide or propane gas to enter the living quarters.
Product
CROSSROADS — CROSSROADS CRUISER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0210-2019·2018-10-31
Siemens APTIO Rack Input Module Recall for Missing Pacemaker Warning
Siemens Healthcare Diagnostics is recalling 441 APTIO Rack Input Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
APTIO RACK INPUT MODULE
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0272-2019·2018-10-31
Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems Due to Software Anomalies
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to reported software anomalies affecting startup, motion control, and image acquisition.
Product
O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027R SYS PRODUCT RWK, Model Number Bl70000027R Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits from 2D…
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0208-2019·2018-10-31
DePuy Mitek Screw and Washer Depth Gauge Recalled for Design Offset
DePuy Mitek is recalling 401 Mitek Screw and Washer Depth Gauges because a design offset causes readings to be approximately 3.2mm shorter than the actual bone hole length.
Product
Mitek Screw and Washer Depth Gauge, Product Code 219024
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19711·2018-10-31
CFMOTO Recalls 2018 ZFORCE Recreational Off-Highway Vehicles Due to Crash Hazard
CFMOTO is recalling approximately 1,800 2018 ZFORCE recreational off-highway vehicles because the throttle pedal may fail to return to idle, posing a crash risk.
Product
Recreational off-highway vehicles (ROVs)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0207-2019·2018-10-31
Howmedica Recalls Tritanium TL Steerable Inserter Due to Locking Mechanism Failure
Howmedica Osteonics Corp. is recalling 58 units of the Tritanium TL Steerable Inserter because the locking mechanism may fail to function as intended due to lack of lubrication.
Product
Tritanium TL Steerable Inserter, Cat. No. 48930000, UDI 07613327381900 Product Usage: The TL Steerable Inserter is a Class 1 instrument which is provided in a non-sterile condition. The inserter is designed to enter the disc space, with a fixed engagement between the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0216-2019·2018-10-31
Siemens StreamLab Refrigerated Storage Module Recall for Missing Warning Label
Siemens Healthcare Diagnostics is recalling StreamLab Refrigerated Storage Module 9000 units because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
STREAMLAB - REFRIGERATED STORAGE MODULE 9000
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0212-2019·2018-10-31
Siemens APTIO 15000 Refrigerated Storage Module Recall for Missing Warning Label
Siemens Healthcare Diagnostics is recalling 441 APTIO 15000 Refrigerated Storage Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
APTIO 15000 REFRIGERATED STORAGE MODULE
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0215-2019·2018-10-31
Siemens StreamLab Automation Modules Recalled for Missing Pacemaker Warning Label
Siemens Healthcare Diagnostics is recalling 186 StreamLab Automation Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
STREAMLAB CORE UNIT / LYNX WITH IOM
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0278-2019·2018-10-31
Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems Due to Software Anomalies
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to software anomalies affecting startup, communication, and imaging functions.
Product
O-arm 1000 2nd Edition Imaging System, BASE OARM Bl70000027230R SYSTEM 230V RWK, Model Number Bl70000027230R Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits…
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0204-2019·2018-10-31
ESAOTE MyLab Alpha Ultrasound System Recalled for Probe Overheating Risk
ESAOTE S.P.A. is recalling 10 MyLab Alpha Model 7400 ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.
Product
MyLab Alpha, Model 7400
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0234-2019·2018-10-31
Ecolab Recalls Da Vinci Robotic System Disposable Accessory Kits
Ecolab is recalling specific lots of Disposable Accessory Kits for the Da Vinci Si Robotic system because wrinkles in the packaging seal could compromise sterility.
Product
Disposable Accessory Kit, 4-Arm (Box of 5) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system / Distributed by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V771000·2018-10-31
Kia Recalls 2019 Forte Vehicles for Headlight Aiming Defect
Kia is recalling 2019 Forte vehicles with LED headlights because they may not be aimed correctly, potentially reducing driver visibility and increasing crash risk.
Product
KIA — KIA FORTE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0206-2019·2018-10-31
ESAOTE MyLab Seven Ultrasound System Recalled for Probe Overheating Risk
ESAOTE is recalling 10 MyLab Seven ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.
Product
MyLab Seven, Model 6400
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0199-2019·2018-10-31
Canon MRI Systems Recall Due to SAR Display Error
Canon Medical System is recalling 252 MRI systems because the displayed SAR value may be lower than the actual value, potentially exceeding safety limits.
Product
Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modality that produces cross-sectional transaxial, coronal, sagittal, and oblique images that display anatomic structures of the head or body.
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0232-2019·2018-10-31
Ecolab Camera Arm Drapes Recalled for Potential Sterility Breach
Ecolab is recalling specific lots of Camera Arm Drapes because wrinkles in the packaging seal could compromise the product's sterility.
Product
Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system / Distributed by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to cover/wrap…
Category
Medical Device
Distribution
Distributed nationwide