Recalls distributed in Wyoming
These notices name Wyoming 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.
1,195 stored notices name Wyoming, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Wyoming too — those are in the archive.
Reported Sep 24, 2014
Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Swanson Health Products, Inc.
FDA (openFDA food enforcement)
Reported Sep 23, 2014
Indiana Firm Recalls Uncured Beef Corn Dogs Due To Possible Temperature Abuse
High riskUsing this product could cause serious injury, illness or death — stop using it now.Monogram Frozen Foods
USDA FSIS
Reported Sep 17, 2014
PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2014
Hitachi Echelon Oval MRI system is a diagnostic imaging device (one unit per package) and is intended to provide the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2014
PERSONA The Personalized Knee System Constrained Tibial Articular Surface Provisional BOTTOM with the following: L CD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2014
Cordis EMPIRA NC RX PTCA Dilatation Catheter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
VIDAS D-Dimer Exclusion II, an automated quantitative test for use on instruments of the VIDAS family for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Codman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programmable valve is an implantable device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Codman & Shurtleff, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
IntelliSpace Portal (ISP) DX/HX/EX, IntelliSpace Portal (ISP) IX, and IntelliSpace Portal (ISP) LX SPECT IntelliSpace…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Original Silk Light Soymilk Half Gallon, Distributed by WhiteWave Foods Broomfield, Colorado 80021, UPC 0 25293 60101 7
High riskUsing this product could cause serious injury, illness or death — stop using it now.White Wave Foods, Inc.
FDA (openFDA food enforcement)
Reported Jul 30, 2014
AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Corp.
FDA (openFDA device enforcement)
Reported Jul 30, 2014
Fat free cottage cheese sold under the Knudsen or Kraft brand and packaged in a plastic container with a net weight of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 30, 2014
Taztia XT (Diltiazem HCl) Capsules, 120 mg, Rx, Packaged and labeled as Thiamine. Re-Packaged By: Shamrock Medical…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shamrock Medical Solutions Group LLC
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 30, 2014
Sarns D4 Aortic Arch Cannulae 6.0mm, 7mm & 8mm angled and straight tip with or without side holes and/or luer Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 23, 2014
V-Series Patient Monitoring System, Manufactured for Mindray DS USA, Inc. Used for monitoring of human physiological…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Jul 23, 2014
e.cam camera system. Emission Computed Tomography System used to detect or image the distribution of radionuclides in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
The Hospira MedNet Medication Management Suite (MMS). Product Usage: The Hospira MedNet Medication Management Suite…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
PALL Medical Breathing Circuit Filter, REF BB50T and BB50T-BULK , Rx ONLY Single use, bi-directional bacterial/viral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pall Corporation
FDA (openFDA device enforcement)
Reported Jul 16, 2014
The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Coca Cola Vanilla, 12 pack/12 fl oz cans, UPC: 49000 03124, Canned under authority of the Coca Cola Company, Atlanta,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Coca-Cola Company
FDA (openFDA food enforcement)
Reported Jul 9, 2014
Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
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.