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 Jul 20, 2022

epoc BGEM Test Card 25 Test Cards/box. In vitro diagnostic device for the quantitative testing of samples of…

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

Siemens Healthcare Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC,…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Ventana HE 600 System, automated slide preparer, for use in laboratories.

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

Ventana Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02), Medium (Model No #15-2814/03), and Large (Model No…

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

Waldemar Link GmbH & Co. KG (Mfg Site)

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000

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

Zeltiq Aesthetics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…

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

Covidien LLC

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

ABL800 Flex Analyzer Model Numbers 393-800 and 393-801

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

Atrium Firm PVC Thoracic Catheter 28French-Intended to facilitate the evacuation of air and/or fluid from the chest…

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

Atrium Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP…

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

Getinge USA Sales Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 6, 2022

PurAqua Belle Vie SPARKLING WATER wellness RELAX 100mg ASHWAGANDHA PER 12 FL OZ STRAWBERRY CUCUMBER FLAVORED SPARKLING…

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

Independent Beverage Company LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 6, 2022

Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797

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

Volcano Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2022

Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural & Artificial Flavor, 33.8 FL OZ (1.05…

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

Abbott Laboratories

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 29, 2022

REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2022

Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk, Soy, Wheat Dist. & Sold Exclusively By:…

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

Taylor Farms Retail Inc.

FDA (openFDA food enforcement)

Food

Reported Jun 22, 2022

Pedialyte***Replaces Electrolytes***Great for Kids and Adults***Strawberry Lemonade Natural Flavor with Other Natural…

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

Abbott Laboratories

FDA (openFDA food enforcement)

Medical devices

Reported Jun 22, 2022

illumina REF DX-410-1001 Model: MiSeq Dx illumina REF 15036706 Model: MiSeq Dx illumina REF 20014053 Model: MiSeq Dx

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

Illumina, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 22, 2022

Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1,…

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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2022

(1) JOBST Compri2, REF 76271-01, containing 2 components, one plastic-wrapped padding and one plastic-wrapped…

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

BSN Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2022

DJO EMPOWR 3D Knee (Right) 10mm Tibial Insert, REF: 342-10-708

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

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2022

Back up batteries in Ventilators labeled as the following: a. CARESCAPE R860 Ventilators (K142679) b. ENGSTROM…

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

GE Healthcare, LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2022

Triathlon Tritanium Tibial Component (Size 6); Catalog Number 5536-B-600 Triathlon¿ Tritanium¿ Tibial Component (Size…

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

Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2022

STORZ KARL STORZ-ENDOSKOPE REF 11272VUE CMOS Video Cysto-Urethroscope REF 11272VUEK CMOS Video Cysto-Urethroscope…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Food

Reported Jun 15, 2022

POTATO SWEET PEELED 2/10# (01)10886810715207(10)0016086769 71520 Best if used by: Best if used by: 03/29/22, 04/05/22,…

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

Liberty Fruit Co. Inc. dba Carol's Cuts

20 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 15, 2022

Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green plastic package.

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

The TJX Companies, Inc.

2 more products in this recall

FDA (openFDA food 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.