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 May 3, 2017

ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14.…

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a…

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

Heartware

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in…

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

Orthosoft, Inc. dba Zimmer CAS

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood…

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the…

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

Ulrich Medical USA Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 26, 2017

AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9

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

Advanced Fresh Concepts Corp.

FDA (openFDA food enforcement)

Food

Reported Apr 26, 2017

ChloroFields Micro-greens Asian Mix, Net Wt. 1.5 OZ, packed in clear plastic clamshells

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

ChloroFields

FDA (openFDA food enforcement)

Medical devices

Reported Apr 26, 2017

Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product…

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

Covidien Medtronic

FDA (openFDA device enforcement)

Food

Reported Apr 26, 2017

GUGGISBERG NATURAL CHEESE COLBY INGREDIENTS: Pasteurized Milk, Cultures, Salt, Enzymes, Annatto Color 1 lb, 2 lb, 6 lb…

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

Dutch Valley Food Distributors

11 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 26, 2017

Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # PBP201 - 10-1.2 oz. packets;…

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

Nutiva

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 26, 2017

Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.

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

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Apr 26, 2017

French's Crispy Jalapenos Net Wt. 5 oz. (141.7g), UPC 0 41500 95309 0, French's Food Company.

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

The French's Food Company, LLC SUBS Reckitt Benckiser

FDA (openFDA food enforcement)

Medical devices

Reported Apr 19, 2017

ViperWire Advance Peripheral Guide Wire with Flex Tip, Model No. VPR-GW-FT18. Sterilized with Ethylene Oxide. The guide…

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

da Vinci Xi EndoWrist Suction Irrigator, 8 mm instrument; PN 480299-03; and SOFTWARE, EMBEDDED RLS, IS4000,…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 19, 2017

LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797

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

Nonna Foods

FDA (openFDA food enforcement)

Medical devices

Reported Apr 19, 2017

Specimen Gate Laboratory; Product Number: 5002-0180 Specimen Gate Laboratory is intended for use as a data processing…

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

PerkinElmer Life and Analytical Sciences, Wallac, OY

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.

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

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 12, 2017

DX-D600 - DXD Imaging Package

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

AGFA Healthcare Corp.

FDA (openFDA device enforcement)

Food

Reported Apr 12, 2017

Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.5 OZ. AND Chokland Mork Dark Chocolate 70%, Net Wt. 3.5 OZ.…

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

Ikea North America Srvcs Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 12, 2017

Mobile Diagnostic X-Ray System with Digital Panel

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

Philips Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 12, 2017

BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector…

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

Philips Medical Systems (Cleveland) Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2017

AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for use in providing diagnostic quality images to…

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

AGFA Healthcare Corp.

FDA (openFDA device enforcement)

Food

Reported Apr 5, 2017

Parmesan Truffle Salt. The product is packaged in glass taster cork jars (0.9 oz.) with cork top lid, glass small jars…

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

Bitterman and Sons

FDA (openFDA food enforcement)

Medical devices

Reported Apr 5, 2017

JResultNet drivers using ASTM coding language. Calculator/data processing module, for clinical use - Stand-alone…

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

Data Innovations, LLC

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.