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.
Reported Oct 15, 2014
McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Information Solutions LLC
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Amiodarone HCl Injection, 450 mg/9 mL (50 mg per mL), 9 mL Single-Use Vial, Rx only, Manufactured for Mylan…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson
FDA (openFDA drug enforcement)
Reported Oct 15, 2014
Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nemschoff Chairs, Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat sealed with label on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthohelix Surgical Designs Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
The Hulka Clip is a sterile packaged medical device that carries a two year expiration date. It is packaged two clips…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf Medical Instruments Corp.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Protocol 10% NBF Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Richard-Allan Scientific Company
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Biosense Webster's Reprocessed SOUNDSTAR¿ eco Diagnostic Ultrasound Catheters, Catalog Nos: M-5723-115, Model Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sterilmed, Inc.
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceutical Co., Ltd.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eugene Oregon, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 8, 2014
GE Healthcare Precision 500D, Classical R&F System. Product Usage: The Precision 500D R&F X-ray System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumed International, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Verigene BC-GP Kit (Catalog number 20-005-018); 1) 20 Verigene BC-GP Test Cartridges; are qualitative multiplexed in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nanosphere, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer medical…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex Medical
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Basil Pesto Pasta packaged in a non-flex plastic tub, net wt 8 oz. A green sticker is placed on the lid of the package…
High riskUsing this product could cause serious injury, illness or death — stop using it now.TJs Place
FDA (openFDA food enforcement)
Reported Oct 8, 2014
Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Natural Blue Diamond Almonds Artisan Nut-Thins crafted with brown rice, almonds & Chia Seeds Wheat & Gluten free Net…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Diamond Growers
FDA (openFDA food enforcement)
Reported Oct 1, 2014
CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is designed for use on patients who require…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 203, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Lakewood Organic Fresh Pressed GMO Free Pure Apple Cold Pressed Not from Concentrate Juice Fruit 32 FL OZ (1 QT) 946 mL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Florida Bottling, Inc.
FDA (openFDA food enforcement)
Reported Oct 1, 2014
STAT 2 Flow Controller; 80" (203 cm) Appx 14.8 mL, 20 Drop Primary Set w/2 Clave, STAT 2 Flow Controller, Rotating…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ICU Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instratek, Incorporated
FDA (openFDA device enforcement)
Reported Oct 1, 2014
The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN), performed using the sample-to-result Verigene…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nanosphere, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pdg Product Design Group Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a polyester [poly(ethylene terephtalate)]…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Peters Surgical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Spacelabs Medical Patient Monitor is a Physiological, Patient monitor With Arrhythmia Detection or Alarms. The Models…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
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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.