Recalls distributed in Kansas
These notices name Kansas 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.
2,850 stored notices name Kansas, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Kansas too — those are in the archive.
Reported Dec 12, 2018
16 count Smartfood Delight Variety Pack Sack
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 12, 2018
Artis Zee and Zeego, model no. 10272462 AXIOM Artis zee/Zeego is a family of dedicated angiography systems developed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 5, 2018
Ultra Dark Chocolate Amaretto Rainier Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Chukar Cherry Company
4 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 28, 2018
The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Nov 28, 2018
Roasted Corn Salsa; Net Weight: 10 lbs. (10 x 1 lb. bags) Corner Bakery Caf¿ Brand Ingredients: Corn, Red Onion,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cadence Gourmet LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 28, 2018
Irrisept OR, Finished Bottle Assembly 450 ml STEP 1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
FDA (openFDA device enforcement)
Reported Nov 21, 2018
3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
ERBITUX CETUXIMAB Injection, 200 mg/100 mL (2 mg/mL), 100 mL per single-use vial, Rx only, Manufactured by: ImClone…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Eli Lilly & Co.
FDA (openFDA drug enforcement)
Reported Nov 21, 2018
GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Nov 21, 2018
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
Stryker Sustainability Solutions LASSO NAV eco Reprocessed Diagnostic EP Catheters designed to obtain…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Nov 21, 2018
simple truth organic Red Quinoa Ingredients: organic red quinoa Distributed by The Kroger Co, Cincinnati, OH…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Kroger Co.
FDA (openFDA food enforcement)
Reported Nov 21, 2018
Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2018
Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate stenoses in iliac, femoral,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Nov 14, 2018
FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Implants Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Nov 14, 2018
TB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F for Curve Type Straight, Atrial J, 60 degree Curve, and Right…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oscor, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2018
EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Zilver 518 Biliary Stent 4mm x 20mm, Catalog Number: ZIB5-125-4.0-20 Product Usage: The Zilver 518 and 635 Biliary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Medical Incorporated
38 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Hy-Vee Spinach, Tomato, Mozzarella Twice Baked Potatoes, Net Wt. 5 oz wrapped in clear plastic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.D & D Foods, Inc.
FDA (openFDA food enforcement)
Reported Nov 7, 2018
Organic Mind Body and Soul - Breakfast Blend Decaf, packaged in 2.25 oz. pillow packs.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Equal Exchange Cooperative dba Equal Exchange, Inc.
FDA (openFDA food enforcement)
Reported Nov 7, 2018
EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable Bone Growth Stimulator is indicated in the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
BACT/ALERT VIRTUO system, A Unit, with Version R2.0 Firmware Product Usage: The BacT/ALERT VIRTU Microbial Detection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
2 more products in this recall
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.