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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 Apr 21, 2021

Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product…

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

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Apr 21, 2021

Evolve Cell Culture Bags, part numbers: EV1000N and EV3000N The Evolve bag is made of Ethyl Vinyl Olefin (EVO) and…

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

OriGen Biomedical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 14, 2021

Amicus MNC Apheresis Kit - Double Needle - Product Usage: intended for use in the collection of blood components and…

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

Fenwal Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 14, 2021

Synapse PACS - Radiological Image Processing System - Product Usage: intended for use, as a web based application, on…

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

Fujifilm Medical Systems U.S.A., Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 14, 2021

Quaker Rice Crisps Sweet Barbecue Flavor, 3.03 oz. bag, UPC 0 30000 31984 0

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

The Quaker Oats Company

FDA (openFDA food enforcement)

Food

Reported Apr 14, 2021

Tippin's Country Gravy, Net Wt 16 OZ, Keep Refrigerated, Tippin's Gourmet Pies LLC, Kansas City, KS UPC 6 80816 12023 1…

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

Tippins

FDA (openFDA food enforcement)

Medical devices

Reported Apr 7, 2021

ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually packaged femoral, tibial and patellar components…

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

DePuy Orthopaedics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 7, 2021

Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to…

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

Hollister Incorporated

FDA (openFDA device enforcement)

Food

Reported Apr 7, 2021

Land O Lakes Queso Bravo White Cheese Dip with Jalapeno and Red Peppers. Net Wt 5 lbs. (2.26kg), UPC 34500-48238.…

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

Land O'Lakes, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 7, 2021

Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note - for definition of the…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

Operating Table System

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

Getinge Group Logistics America, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected…

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

Stryker Communications

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is…

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

Teleflex Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 24, 2021

CyberKnife Treatment Delivery System - Product Usage: indicated for image-guided stereotactic radiosurgery and…

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

Accuray Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Mar 24, 2021

Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization Table CAT-880B Canon CATHETERIZATION TABLE,…

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

Canon Medical System, USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination of methamphetamine in oral fluid, PN…

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

OraSure Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

Dimension Vista HDLC - colorimetric method, lipoproteins - Product Usage: used as an aid in the diagnosis of lipid…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular Ultrasound Catheter is a component of the ACIST…

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

Acist Medical Systems

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible w/Short Stem Pessary, REF MXKPGSS2-1/4, 2-1/4"…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no…

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

Hamilton Co.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/…

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

Nihon Kohden America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

Infusion Pump

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

Baxter Healthcare Corporation

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.