All recall categories

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.

Medical devices

Reported Oct 2, 2019

APS Accelerator modular systems, 208-230 V-, 50/60 Hz, 1800 VA, IVD, RX, Class 2 Laser Product,

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2019

Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2019

Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2019

Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2019

LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2019

One-Half Gallon Hiland Dairy Lemonade UPC: 72060-00519-6 packaged in plastic bottle and Pint Hiland Dairy Lemonade UPC:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hiland Dairy Foods

FDA (openFDA food enforcement)

Food

Reported Sep 25, 2019

Ore Ida Spud Bites, packaged in 5lb. plain poly foodservice bags, six bags per case, frozen, Case UPC: 1 00 72714 00093…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

McCain Foods USA

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2019

Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Allergan PLC

14 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2019

PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Natures One Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2019

XP- CR Tibial Tray- Interlok 59mm Item # 195268

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Biomet, Inc.

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Norm-O-Temp model 111Z

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cincinnati Sub-Zero Products LLC, a Gentherm Company

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 10, 2019

Hy-Vee Fresh Commissary Recalls Ready-To-Eat Beef and Chicken Products Due to Misbranding and Undeclared Allergens

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hy-Vee Fresh Commissary

USDA FSIS

Medical devices

Reported Sep 4, 2019

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2019

Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Phadia Ab

FDA (openFDA device enforcement)

Food

Reported Sep 4, 2019

PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

PreGel America, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 4, 2019

Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

Kit BD Max Check-Points CPO IVD EU; Catalog # 278102

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (20 mm) 9630TF20…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Edwards Lifesciences, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 28, 2019

PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 oz

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Kroger Co.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 21, 2019

Amy's Bowls - Broccoli & Cheddar Bake; Net Wt. 9.5 oz. (269g) Perishable - Keep Frozen. Microwave or regular oven. UPC:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amys Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 21, 2019

BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number: 367001 Product Usage: Blood Alcohol…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

FDA (openFDA device 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.