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 48,122 notices were distributed nationwide, so they reach Washington too — those are in the archive.

Food

Reported Nov 21, 2018

MarieBelle brand Japanese Matcha Japanese Green Tea and White Chocolate Bar, NET Wt. 2.82 oz. UPC code: 877708005886

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

Maribel's Sweets, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 21, 2018

The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option

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

Stryker Medical Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 21, 2018

simple truth organic Red Quinoa Ingredients: organic red quinoa Distributed by The Kroger Co, Cincinnati, OH…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

The Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 21, 2018

Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of…

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

Zimmer Biomet, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Nov 17, 2018

Swift Beef Company Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination

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

Swift Beef Company

USDA FSIS

Medical devices

Reported Nov 14, 2018

BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva Catheter), Catalog Number 383539 Product Usage:…

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

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Catalog Number: P2845B Dental Posts are implanted into…

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

Coltene Whaledent Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 14, 2018

Product 8x8 " individually packaged in black plastic trays with clear plastic dome lid is cornbread and it was…

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

Fred Meyer Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 14, 2018

Centricity PACS-IW with Universal Viewer version 5.0.x with PACS-IW foundation displays medical images (including…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 14, 2018

New Seasons Market Hot & Sour Broth, packaged in 24 oz glass jar. UPC 840600108672

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

New Seasons Market LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 14, 2018

REF VV19F Reinforced Dual Lumen Cannula, 19Fr., Sterile EO, DISPOSABLE: DO NOT RE-USE CE 0473 Product Usage: The OriGen…

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

OriGen Biomedical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

TB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F for Curve Type Straight, Atrial J, 60 degree Curve, and Right…

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

Oscor, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

EZ1 Advanced XL, Model Number: 9001492, GTIN: 04053228010760 Product Usage: The EZ1 Advanced XL is designed to perform…

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

3M Fast Release Varnish, 5% Sodium Fluoride, Mint Flavor, Rx Only, single use. 200 pack, with each package containing 1…

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be…

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

Baxter Healthcare Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364, 44336409 (Repaired Reader spare part) - Product…

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

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1, Class I, 1 Quart (946ml) REF:3306. Product Usage - Impak Elastic…

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

CMP Industries, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

Zilver 518 Biliary Stent 4mm x 20mm, Catalog Number: ZIB5-125-4.0-20 Product Usage: The Zilver 518 and 635 Biliary…

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

Cook Medical Incorporated

38 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 7, 2018

S & W White Beans, Net Wt 15 oz (425g), UPC 72273-38807. Distributed by Faribault Foods, 1818 2nd Ave NW, Faribault, MN…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Faribault Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 7, 2018

Forager Project Organic Protein Plant Shake Nuts & Vanilla 12 fl oz. UPC: 8 14558 02038 6

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

Forager Project LLC

FDA (openFDA food enforcement)

Food

Reported Nov 7, 2018

Spinach and Mushroom Pie, Net Wt. 6 OZ, packaged in a paper carton, Keep Frozen

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

Lone Star Bakery, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 7, 2018

EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable Bone Growth Stimulator is indicated in the…

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

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

NucliSENS¿ Magnetic Extraction Reagents

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

BioMerieux SA

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.