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 Jun 7, 2017
Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Trident Item # 421048, Multi-Grain Alaskan Cod, Frozen, RETAIL packages, Net wt. 12 oz. UPC 0 28029 21048 4 The retail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trident Seafoods Corp. - Island Enterprise M/V
7 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 7, 2017
Dolphin Inflation Device, REF 0185NA. Rx only, Sterilized using Ethylene Oxide. DOLPHIN is a single-use, sterile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 2, 2017
Correctional Industries Airway Heights Food Operations Recalls Frozen Meat and Poultry Products Due to Water…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Correctional Industries Food Factory
USDA FSIS
Reported May 31, 2017
Ceftriaxone TX 32 US S30, Ref 412302 and Ceftriaxone TX 32 US F100, Ref 507058 ETEST is a quantitative technique for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 31, 2017
CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 oz. Distributed by: Phoenix Food, LLC. Canton, TX 75103…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Phoenix Food, LLC
FDA (openFDA food enforcement)
Reported May 31, 2017
Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.RB Manufacturing LLC
FDA (openFDA food enforcement)
Reported May 31, 2017
ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ ARTISAN-STYLE PIZZA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 31, 2017
Herbal Tea Variety 120 ml/pouch, 40 pouches/case
High riskUsing this product could cause serious injury, illness or death — stop using it now.U S Deer Antlers Export & Import
FDA (openFDA food enforcement)
Reported May 31, 2017
Sugar Crackers 400g (14.1oz) x 12 packets per carton/case, UPC 9556184 500023
Moderate riskThis product could cause temporary or reversible health problems — stop using it.U-Can Food Trading Inc.
FDA (openFDA food enforcement)
Reported May 26, 2017
Cauldron Soups, LLC Recalls Beef Broth Products Produced Without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Somi Foods, Inc.
USDA FSIS
Reported May 24, 2017
SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 24, 2017
ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 24, 2017
GIZA Vertebral Body Replacement
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eden Spine Europe SA
FDA (openFDA device enforcement)
Reported May 24, 2017
Label reads in part "***Full Tilt Ice Cream Fudge Brownie Swirl Vegan***one pint***Ingredients: Coconut Milk (coconut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Full Tilt Ice Cream
FDA (openFDA food enforcement)
Reported May 24, 2017
Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Orthosoft, Inc. dba Zimmer CAS
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 24, 2017
NexGen Offset Stem Extension, sizes 14mm and 17mm For use in total arthroplasty.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2017
The Osso Good Co. Recalls Beef and Pork Products Produced Without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Yosemite Protein Products, Inc.
USDA FSIS
Reported May 17, 2017
Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Almore International Inc.
FDA (openFDA device enforcement)
Reported May 17, 2017
Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2017
CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 17, 2017
NDI P7 Position Sensor, Stereotaxic Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosoft, Inc. dba Zimmer CAS
FDA (openFDA device enforcement)
Reported May 17, 2017
Frozen Wild Shrimp Burgers, Wild Grill Foods brand, net wt. 12 oz. Each package contains 4/ 3 oz. pieces. UPC 8 94067…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unisea Inc.
FDA (openFDA food 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.