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 48,122 notices were distributed nationwide, so they reach Kansas too — those are in the archive.
Reported Dec 14, 2016
Xcela Power Injectable PICC Maximal Barrier Nursing Kit The Maximal Barrier Nursing Kits are Tandem Pack Convenience…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
A&W Cream Soda, 20 FL OZ, Caffeine Free
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chesterman Co.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Cookie Dough Ice Cream packed under the following brand names and sizes: 1. Chocolate Shoppe Ice Cream Company, 3…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Chocolate Shoppe Ice Cream Co., Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Cheese Stick w/Beef Stick Meal Break, Item #61406
High riskUsing this product could cause serious injury, illness or death — stop using it now.E S Foods
19 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Chicken eggs packaged in the following configurations 1) Premium Farm Fresh White Eggs, packaged in 6 count, 10 count,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Good Earth Egg Company
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile), Product Code 44965 NS; C-Section Drape with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay, barbiturate) Product is intended for use by clinical…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.OraSure Technologies, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Brilliance 64 728231 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# ARREZZIO IMPERIAL; UPC: 0 74865 30185 5 Saputo code: #101379 ;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Saputo Cheese USA, Inc.
13 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Perceval Sutureless Aortic Heart Valve size S, Item # ICV1208, REF PVS21; Perceval Sutureless Aortic Heart Valve size…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Greatbatch, Offset Cup Impactor with the following Parts and Catalogue #: Tl0600 ~ MMP3100CHA04 T10491 MIMP3100CHA04…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Greatbatch Medical
FDA (openFDA device enforcement)
Reported Dec 7, 2016
MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche OMNI S Analyzer: cobas b 221<6>Roche OMNI S6 system The Roche…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
12ct Banana Nut mini muffins labeled as 12ct Lemon poppy seed mini muffins; Date code 160803 ink jet printed on top…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cv East LLC, Cornerstone Marion LLC
FDA (openFDA food enforcement)
Reported Nov 30, 2016
DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 18mm Item Code: 186850018 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Organic Cacao Nibs, packaged in 200g (7.05 oz) brown bags, UPC code 661594002032
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Level Ground Trading Limited
FDA (openFDA food enforcement)
Reported Nov 30, 2016
Philips Healthcare System X-ray Tomography Computed :
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wells Enterprises, Inc.
FDA (openFDA food enforcement)
Reported Nov 23, 2016
Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCain Foods USA
FDA (openFDA food enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 18, 2016
Wayne Farms, LLC Retira Productos De Pechuga De Pollo Listos Para Comer Los Cuales Podran Estar Medios Crudos
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Nov 16, 2016
AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
X-Force Nephrostomy Balloon Dilation Catheter Kit with Inflation Device, PTFE Sheath, 8 mm x 15 cm, Product Code 996081…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
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.