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 27, 2017
Spine Referencing Instrumentation, Spinous Process Clamp, Tall When used with a Medtronic StealthStation Navigation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 13, 2017
MOSAIQ Medical Charged-Particle Radiation Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
Toshiba America Medical Systems Ultimax Digital Fluoroscopic X-Ray System Model: DREX-UI80 Ultimax is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Plum 360 Infusion System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,
High riskUsing this product could cause serious injury, illness or death — stop using it now.NatureAll-STF Holding, LLC
7 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 16, 2017
BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 2, 2017
STOCKERT Heater-Cooler System 3T, 230 V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
VIDAS Testosterone, Ref 30418
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Simple truth Dry Roasted Macadamia Nuts 12 oz bags UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Corporate Food Technology Laboratory
FDA (openFDA food enforcement)
Reported Jul 19, 2017
Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Chili Pequino 0.25 oz packaged in a clear plastic bag; Product Code 10106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bolner's Fiesta Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 12, 2017
Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutri-Dyn Midwest, Inc.
FDA (openFDA food enforcement)
Reported Jun 28, 2017
PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Monfitello
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Red Robin Burgers and Brews Crispy Onion Rings, frozen, Net wt. 14 ounce. Retail package UPC 0 43301 61119 3.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lamb Weston Inc.
FDA (openFDA food enforcement)
Reported Jun 7, 2017
Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Scale Mfg Co.
FDA (openFDA device enforcement)
Reported Jun 7, 2017
The Green Herb 100% Natural AL-ER-G, 60 and 150 Capsules, Dietary supplement, This item is packed in a white bottle…
High riskUsing this product could cause serious injury, illness or death — stop using it now.MusclMasster, LLC
FDA (openFDA food enforcement)
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
Spacelabs Healthcare Arkon Anesthesia Delivery System is intended for use in the hospital environment and operating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Mar Reynolds Medical, Ltd.
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)
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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.