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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.

Meat & poultry

Reported Jan 24, 2020

Golden Pearl Trading Corporation Recalls Ready to Eat Imported Siluriformes Products Produced Without Benefit of Import…

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

Golden Pearl Trading Corporation

USDA FSIS

Food

Reported Jan 22, 2020

13 Bean Soup Mix is sold under Bob's Red Mill brand, packaged in Form & Fill (29 oz. and 822 gram), Standup Pouch (29…

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

Bob's Red Mill Natural Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 22, 2020

Dry Garbanzo Beans are sold under different brands and described as follows: -Bulk 2000 lbs. Totes. -CBP brand 25#…

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

Columbia Bean & Produce, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2020

ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2020

QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2020

Butler's Dark Chocolate with Irish Whisky, 3.52oz bar, UPC 8 44984 17619 7, 10 units per case

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

Gourmet International Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2020

Microbiologics QC Sets and Panels, Gram-Positive Blood Culture Control Panel (Inactivated Pellet), Catalog # 8180 Used…

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

Microbiologics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2020

LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…

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

Physio-Control, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2020

Riverpoint Medical 18G Brachy Grid, B&K style, REF RPG-18, Sterile, Rx. The firm name on the label is Riverpoint…

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

Riverpoint Medical, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2020

Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF A1500

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

Teleflex Medical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2020

Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit,…

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

Medical Action Industries, Inc. 306

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2020

Cios Alpha, Model Number 10308191; mobile X-Ray system designed to provide X-ray imaging of the anatomical structures…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 15, 2020

GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152…

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

TFI Holding dba Grey Ghost Bakery

FDA (openFDA food enforcement)

Meat & poultry

Reported Jan 9, 2020

FSIS Issues Public Health Alert for Swedish Meatball Products Due to Misbranding and an Undeclared Allergen

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Carso's Pasta Company

USDA FSIS

Medical devices

Reported Jan 8, 2020

i-STAT cTnI cartridge

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

Abbott Point Of Care Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 8, 2020

Chicken of the Sea Sardines in Water; Net Wt. 3.75 oz. (106g) UPC 0 48000 00707 0 18 Individual items per case…

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

Chicken of the Sea

FDA (openFDA food enforcement)

Medical devices

Reported Jan 8, 2020

Invia Foam Dressing Kit with FitPad - X-Large (3 pcs) SKU # 0876224. The Invia Foam Dressing Kit with FitPad consists…

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

Medela Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2020

O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000

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

Medtronic Navigation, Inc.-Littleton

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2020

HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when…

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

Thoratec Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

STA UNICALIBRATOR (ref. 00675)

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

Diagnostica Stago, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2020

R.H. Macys & Co. Roasted Salted Cherries Berries and Nuts with Dark Chocolate, in 10oz metal tin, UPC - 788709600362

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

Ferris Coffee and Nut Company, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2020

VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…

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

Allergan PLC

3 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.