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.

Food

Reported Dec 9, 2020

Dole" Organic Romaine Hearts 3pk Organic Biologique) (UPC 0-71430-90061-1), Wild Harvest Organic Romaine Hearts, Net Wt…

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

Dole Fresh Vegetables Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 9, 2020

B. Braun Introcan Safety IV Catheters, Product codes REF 4252500-01 4252519-01 4252535-01 4252560-01 4252586-01…

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

Janus Trade Group

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

Luminesse ML PMMA, 98x20mm, REF: 5336-B1 - Product Usage: used as a milling blank in the fabrication of provisional…

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

Talladium Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…

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

Coloplast Manufacturing US, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 2, 2020

Natural Grocers, Elderberries Whole Organic, 4 oz. (113g), plastic bag, UPC 0-0082-00304-3

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

Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers

FDA (openFDA food enforcement)

Food

Reported Nov 25, 2020

FC TOMATOES ROMA DICED 3/8" 1/5#; FC TOMATOES ROMA DICED 3/8" 4/5#, and FC TOMATOES ROMA DICED 3/8" 2/5# all packaged…

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

FreshPoint Dallas

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2020

VNS Therapy¿ AspireSR¿ Generator

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 25, 2020

COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…

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

Merz North America, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2020

Trader Joe's brand Gluten Free Battered Halibut, SKU 00503822. Product of USA. Frozen product is packed in plastic bag…

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

Orca Bay Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 18, 2020

SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…

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

Aesthetics Biomedical, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 18, 2020

J&O Mixed Veggie Cup with Dip, Net Weight 5.0 oz. (128 g), UPC 95631-85818. Mfg By: RDW, Pueblo CO 81001

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

Russ Davis Wholesale, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 18, 2020

Niobe ES System, Models 001-006000-1 and 001-006100-1

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

Stereotaxis Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2020

Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Anesthesia System provides the functional feature…

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

GE Healthcare, LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 4, 2020

CMEAmerica BodyGuard Wall Charger: Lot number 2019-0364, Mode/Catalogue number 151-143XL, *+B 01151143X…

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

CME America LLC

FDA (openFDA device enforcement)

Food

Reported Nov 4, 2020

Eishindo brand "CUP JELLY (MINI); NET WT. 28.2oz (800g); 50pcs; INGREDIENTS: WATER, HIGH FRUCTOSE SYRUP, APPLE JUIC,…

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

Hadson (Toko) Trading Co., Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 4, 2020

Happy Tot Superfoods Gluten Free Oat Bar Organic Blueberries & Oatmeal. SKU: TB-BLOT-5 and TB-BLOT-5-WM. Ready-to-eat…

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

Nurture Inc. dba Happy Family

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 28, 2020

BD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref) No. 383538 BD Nexiva closed IV catheter…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay…

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Langston Dual Lumen Catheter

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

Vascular Solutions, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2020

Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product…

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 21, 2020

Watermelon 10 oz UPC Code: 681131180672; Watermelon 32 oz UPC Code: 681131180689; Watermelon Chunks 42 oz UPC Code:…

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

Country Fresh Inc.

15 more products in this recall

FDA (openFDA food enforcement)

Free recall alerts

Get alerted about new Kansas recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.