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 May 30, 2018
ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U, Rx, Sterile. Incorrect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
First Step Endoscopic Cleaning Pad, 100ml, Flexible Endoscope Bedside Pre-Clean Kit, Catalogue Number EP-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison Polymeric Engineering
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 23, 2018
Zoi Mixed Berry Greek Yogurt Parfait, 9 oz. clear plastic cup, covered with a clear plastic snap-on lid. UPC 8 17203…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.A G Specialty Foods, Inc.
FDA (openFDA food enforcement)
Reported May 23, 2018
Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott
FDA (openFDA device enforcement)
Reported May 23, 2018
DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured and Distributed by eBars, LLC, Franklin, TN 37064…
High riskUsing this product could cause serious injury, illness or death — stop using it now.eBars
12 more products in this recall
FDA (openFDA food enforcement)
Reported May 23, 2018
Tosoh ST AIA-PACK HbA1c, HbA1c Reagent, Pt. No. 025218 The device is designed for In Vitro Diagnostic Use Only for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 23, 2018
Persona Stemmed Tibial Provisional Size H Left, Item Number 42532108301 For use during orthopaedic surgery for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 18, 2018
Hempler Foods Group Recalls Ready-To-Eat Pepperoni Sticks Due to Misbranding and Undeclared Allergen
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hempler Foods Group LLC
USDA FSIS
Reported May 16, 2018
ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported May 16, 2018
BEQ-T 9410 Lurie Chldns Small 1/4, Custom Tubing Kit, Catalog No. 709000430
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datascope Corporation
27 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Shoulder Set is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
FDA (openFDA device enforcement)
Reported May 16, 2018
MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostic Hybrids, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
Arugula Microgreens, Greenbelt Microgreens brand, net wt. 75 gram. Product is packaged in a clear plastic clam shell…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Greenbelt Greenhouse Ltd.
6 more products in this recall
FDA (openFDA food enforcement)
Reported May 16, 2018
Hemodynamic monitoring system (HMS), comprised of a Patient Interface Module (Part Number 58401-000 and a User…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported May 16, 2018
EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MHC Medical Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz (84g); UPC: 853787005368
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Munk Pack Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 16, 2018
ACUSON SC2000 Ultrasound System. The firm name on the label is Siemens Medical Solutions USA, Inc., Buffalo Grove, IL.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
STONEWALL KITCHEN Basil Pesto Aioli Net Weight Net 10.25 oz. UPC: 7 11381 03060 8. Product is incorrectly labeled as…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stonewall Kitchen, LLC
FDA (openFDA food enforcement)
Reported May 16, 2018
Raw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Triangle Pharmanaturals LLC
25 more products in this recall
FDA (openFDA food enforcement)
Reported May 16, 2018
Budget $aver Sugar Free Twin Pops Net Contents 28.2 FL OZ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziegenfelder Company, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 9, 2018
Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
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.