All recall categories

Recalls distributed in Washington

These notices name Washington in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,362 stored notices name Washington, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Washington too — those are in the archive.

Medical devices

Reported Feb 25, 2026

MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN):…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 18, 2026

Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Costco Wholesale Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Feb 18, 2026

Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 18, 2026

Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

McCain Foods USA Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 18, 2026

Brilliance iCT; Product Code (REF): 728306;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 18, 2026

CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018; PEANUT BUTTER NET WT. 0.5OZ & NET…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ventura Foods LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 11, 2026

Repackaged M&Ms Peanut candies, Net Wt 1.3 oz. Item BB471BG. Labeled as Make Your Mark. For nutrition facts information…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beacon Promotions Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2026

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 11, 2026

JUICE from the Raw, DETOX GREENS

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Everpress Juice

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2026

Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number: CL0073 Software Version: Not…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fujirebio Diagnostics, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 11, 2026

Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System Model/Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 11, 2026

MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 11, 2026

spicely ORGANIC garlic salt NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY NO PRESERVATIVES - NO WHEAT NO SUGAR -…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Organic Spices, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 11, 2026

CINNAMON POWDER NET WT : 3.5 oz (100g) PRODUCT OF INDIA UPC 7 46241 29537 8 Distributed by: Venzu Traders LLC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Venzu Traders LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2026

Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk Magnifying Lens, Catalog VMD

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Vortex Surgical Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 11, 2026

WinCo Foods Deli Margherita Pizza Thin Crust, Item #67279. Net wt. 17oz. UPC 0267279 807987. Product is Take & Bake and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

WinCo Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 4, 2026

PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cerapedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 4, 2026

BEAR Implant. Model Number: 1000.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Miach Orthopaedics

FDA (openFDA device enforcement)

Medical devices

Reported Feb 4, 2026

Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conductivity…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

NIPRO Technical Services, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 4, 2026

Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Ireland, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merit Medical Systems, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.