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.

Medical devices

Reported May 29, 2019

DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is…

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

KaVo Dental Technologies LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

Thio Med w/Dex, Hem, Vit K (5ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general…

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

Remel Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106

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

Zimmer GmbH

75 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent…

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

Abbott Ireland Diagnostics Division

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S

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

Compass Health Brands (Corporate Office)

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 22, 2019

Item #13898 Raw California Orange Blossom Honey, packaged in an 18 oz jar with gold metal lid. Retail Jar UPC: 0 30042…

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

Glorybee Natural Sweeteners, Inc.

FDA (openFDA food enforcement)

Food

Reported May 22, 2019

Frozen ground tuna, 1 lb package, 20 packages/case

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

Jensen Tuna Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 22, 2019

Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021

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

Moller Vital

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

Pentax Medical C2 CryoBalloon Standard Focal Catheter, Model FG 1028, Sterile, RX. Product Usage: The C2 CryoBalloon…

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

Pentax

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of…

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

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

M200 Fall Monitoring System

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

Stanley Security Solutions Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2019

Abbott ARCHITECT cSystems ICT Module, REF 09D28-03. Product Usage: The ARCHITECT cSystems ICT (Integrated Chip…

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

Abbott Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported May 15, 2019

Frozen Poppy Seed Bread (57 grams), UPC Codes: (01)03556420003673(15)191122(10)181122(91)0937326, Lot 22112018

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

Laduree USA

FDA (openFDA food enforcement)

Food

Reported May 15, 2019

Dried whole elderberry, Oregon s Wild Harvest brand, packaged in metalized plastic bag, net wt. 4 oz or 1 lb. Each case…

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

Oregons Wild Harvest Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 15, 2019

Atellica IM 1300 Analyzer, Material Number 11066001

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

Siemens Healthcare Diagnostics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 15, 2019

Dragonfly Dehydrate Guava Ing: Guava, Sugar, Salt Net Wt: 5.25 ozs 150g Distributed by: U.S. Trading Company Product of…

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

U.S. Tov, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 15, 2019

T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off…

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

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2019

Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), product code 35700BAX - Product Usage: The…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2019

FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116),…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported May 8, 2019

Fannie May Pixies , Caramel and Pecan Clusters covered in Milk Chocolate 14 oz. Box - 12 units per case

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

Fannie May Confections Brands, Inc.

FDA (openFDA food enforcement)

Food

Reported May 8, 2019

Yellow Corn Flour #620, Unenriched, packaged in bulk and 50 lb bags

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

Iowa Corn Processors

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 8, 2019

EZ Derm Porcine Xenograft, labeled as the following: a. EZ Derm 3x4 (8x10 cm) Non-Perforated, Part Number: 131703-03;…

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

Molnlycke Health Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2019

cobas e 801 immunoassay analyzer

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

Roche Diagnostics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2019

Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT) These devices are indicated for resection of soft and osseous…

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

Arthrex, Inc.

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.