State

Washington product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49951–49975 of 82369

HighFDA (Devices)·Z-0972-2017·2017-01-18
Siemens Recalls Artis Q Angiographic X-Ray Systems for Generator Defects
Siemens is recalling Artis Q angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.
Product
Artis Q/Q.zen, Angiographic x-ray system Stand alone system The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1235-2017·2017-01-18
Cheese Club Mac and Cheese Recalled for Salmonella Risk
Fourth Street Barbecue is recalling Cheese Club mac and cheese products because milk powder ingredients may be contaminated with Salmonella.
Product
Cardboard sleeve: Cheese Club express mac Macaroni & Cheese Dinner, Four 2.05 OZ Bowls; Net Wt. 8.2 OZ.; Distributed by: Aldi, Inc., Batavia, IL 60510
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-0988-2017·2017-01-18
ICU Medical Recalls Tego Connectors Due to Potential Leaking Risk
ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.
Product
Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0868-2017·2017-01-18
Koi Palace Mini Mooncakes Recalled for Undeclared Allergens
Magic Gourmet Trading Inc. is recalling Koi Palace Mini Mooncakes due to missing ingredient labels and undeclared wheat, peanut oil, and egg yolk.
Product
Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini White Lotus Seed Paste w/ Egg Yolk Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
Category
Food
Distribution
3 states
HighFDA (Food)·F-0859-2017·2017-01-18
Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens
Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes because they lack adequate labeling for undeclared allergens including wheat, gluten, eggs, milk, peanuts, pine nuts, almonds, walnuts, and sesame.
Product
Koi Palace Mini Moon Cake: 8 Mini Treasures Combo Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0963-2017·2017-01-18
Stryker Recalls Reprocessed Ablation Catheter Cables Due to Sterility Concerns
Stryker is recalling reprocessed ablation catheter cables because a breach in sterile packaging may have resulted in non-sterile product.
Product
Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as electrode cables with a multi-pin connector on the distal end which connects to an ablation catheter and a multi-pin connector on the proximal end which connects…
Category
Medical Device
Distribution
35 states
HighFDA (Devices)·Z-1005-2017·2017-01-18
Philips Clinix RF Plus X-ray System Recalled for Tilt Hazard
Philips is recalling 41 Clinix RF Plus X-ray systems because liquid penetration can cause an unintentional tilt of the diagnostic table.
Product
FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·17V040000·2017-01-18
Nissan Recalls 2015-2017 Altima Vehicles for Rear Door Latch Defect
Nissan is recalling 2015-2017 Altima vehicles because improperly routed rear door latch cables may allow doors to open while driving, increasing injury risk.
Product
NISSAN — NISSAN ALTIMA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1013-2017·2017-01-18
Beckman Coulter Recalls UniCel DxH 800 Cellular Analysis System
Beckman Coulter is recalling the UniCel DxH 800 Cellular Analysis System because it may fail to detect blasts in some blood samples.
Product
UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B68304
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0869-2017·2017-01-18
Koi Palace Mooncakes Recalled for Undeclared Allergens and Labeling Defects
Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to inadequate labeling and undeclared allergens including wheat, walnut, pine nut, sesame, and egg yolk.
Product
Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Fresh Five Nuts with Smoked Ham Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0951-2017·2017-01-18
Natus Warmette Blanket and Dual Cabinets Recalled for Fuse Failure
Natus Manufacturing Limited is recalling 31 Warmette Blanket and Dual Cabinets because a fuse may blow, causing power loss and potential melting of the fuse cover.
Product
Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette Blanket Cabinet is designed to store and warm blankets and hospital linens; while, the Natus Warmette Dual Cabinet is designed to store and warm blankets and hospital linens in one compartment and…
Category
Medical Device
Distribution
12 states
HighFDA (Food)·F-0860-2017·2017-01-18
Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens
Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to missing ingredient and allergen labels. The product contains undeclared wheat, walnuts, and pine nuts.
Product
Koi Palace Mini Moon Cake: Five Nuts with Smoked Ham & Egg Yolk Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
Category
Food
Distribution
3 states
HighFDA (Food)·F-0872-2017·2017-01-18
Koi Palace Mini Mooncakes Recalled for Undeclared Allergens
Magic Gourmet Trading Inc. is recalling Koi Palace Mini Mooncakes because they lack adequate labeling, including undeclared wheat, walnut, pine nuts, pumpkin seeds, and sesame.
Product
Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Black Truffles with Five Nuts. Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
Category
Food
Distribution
3 states
HighNHTSA·17V039000·2017-01-18
Forest River Recalls 2017 Prime Time Avenger RVs for Tire Placard Errors
Forest River is recalling 2017 Prime Time Avenger recreational vehicles because incorrect Federal Placards may lead to tire over-inflation and blowouts.
Product
FOREST RIVER — FOREST RIVER AVENGER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0871-2017·2017-01-18
Koi Palace Mini Mooncakes Recalled for Undeclared Wheat Allergen
Magic Gourmet Trading Inc. is recalling Koi Palace Mini Mooncakes because the products lack adequate labeling, including undeclared wheat.
Product
Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Wolfberry & Dates Paste. Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
Category
Food
Distribution
3 states
ModerateFDA (Devices)·Z-0965-2017·2017-01-18
ASP Recalls EVOTECH Endoscope Cleaner Due to Hose Leak Risk
Advanced Sterilization Products is recalling 107 EVOTECH Endoscope Cleaner and Reprocessor Systems because a hose may come loose and cause a leak.
Product
EVOTECH Endoscope Cleaner and Reprocessor System 208V, Product Code: 50004 The EVOTECH ECR Endoscope Cleaner and Reprocessor, a washer/disinfector, is indicated for use with high-level disinfectant CIDEX OPA Concentrate Solution and an enzymatic detergent (CIDEZYME XTRA) to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1017-2017·2017-01-18
Merge Eye Station Software Recalled for Potential Data Deletion
Merge Healthcare is recalling Merge Eye Station software versions 11.6.0 and prior due to a risk of accidental patient record deletion.
Product
Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager distributed by Ophthalmic Imaging Systems (OIS). Versions: 11.6.0 and prior
Category
Medical Device
Distribution
52 states
ModerateFDA (Devices)·Z-1002-2017·2017-01-18
Siemens Biograph mCT Flow 40-4R Laser Cover Window Recall
Siemens Medical Solutions is recalling Biograph mCT Flow 40-4R scanners because laser cover windows may fall off.
Product
Biograph mCT Flow 40-4R, Material Number 10529159 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0957-2017·2017-01-18
Straumann Dental Implant Drills Recalled for Tolerance Specification Failures
Straumann Manufacturing is recalling 165 dental implant drills because they cannot be inserted into handpieces due to tolerance specification failures.
Product
Straumann Drill 1, short, ¿ 2.2mm, l 33.0mm, SS-Non sterile. Dental implant accessory Article Number: 044.210 Dental implants drill accessory is intended to prepare osteotomy site for surgical dental implant placement. Dental implants are intended for immediate placement…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0979-2017·2017-01-18
Siemens Recalls Intact PTH Assay Kits Due to Negative Bias
Siemens is recalling IMMULITE 2000 Intact PTH assay kits because they may show a negative bias of up to -39% at low concentrations.
Product
SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test Code iPTH, REF/Catalog Number L2KPP2, Siemens Material Number (SMN) 10381441 and REF/Catalog Number L2KPP6, SMN 10381442; IVD --- Made in UK -- Siemens healthcare Diagnostics Products Ltd. Glyn…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0975-2017·2017-01-18
GE OEC Mobile Fluoroscopy Systems Recalled for Power Cable Failures
GE Healthcare is recalling OEC 9900 Elite and other mobile fluoroscopy systems because the workstation power cable assembly can fail intermittently.
Product
The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedure. Examples of clinical application may include cholangiography, endoscopy, urologic, orthopedic…
Category
Medical Device
Distribution
50 states
ModerateFDA (Devices)·Z-1001-2017·2017-01-18
Siemens Biograph mCT Flow Edge-4R Scanner Recall for Laser Cover Windows
Siemens Medical Solutions is recalling one Biograph mCT Flow Edge-4R scanner because laser cover windows may fall off.
Product
Biograph mCT Flow Edge-4R, Material Number 10528955 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0999-2017·2017-01-18
Siemens Biograph mCT-X Scanner Recall Due to Falling Laser Cover Windows
Siemens Medical Solutions is recalling Biograph mCT-X scanners because laser cover windows may fall off.
Product
Biograph mCT-X w/TrueV Upgrade, Material Number 10250745 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0995-2017·2017-01-18
Siemens Biograph mCT Scanners Recalled for Falling Laser Cover Windows
Siemens Medical Solutions is recalling 88 Biograph mCT scanners because laser cover windows may fall off.
Product
Biograph mCT S(40)-4R, Material Number 10248671 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0958-2017·2017-01-18
Straumann Twist Drill PRO Recalled for Tolerance Specification Defects
Straumann Manufacturing is recalling 120 units of Twist Drill PRO dental implant accessories because they cannot be inserted into handpieces due to tolerance specification failures.
Product
Straumann Twist Drill PRO ¿4.2mm,long,41mm,SS-Non sterile. Dental implant accessory Article Number: 044.255 Dental implants drill accessory is intended to prepare osteotomy site for surgical dental implant placement. Dental implants are intended for immediate placement and…
Category
Medical Device
Distribution
Distributed nationwide