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.

2,889 stored notices name Kansas, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Kansas too — those are in the archive.

Medical devices

Reported Apr 22, 2026

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

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

Integra LifeSciences Corp. (NeuroSciences)

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

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

Linkbio Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2026

Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count…

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

Blueroot Health, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2026

Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor

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

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

BD Kiestra" ReadA; Catalog No.: 446948.

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

Bd Kiestra Lab Automation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved…

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

Intuitive Surgical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)

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

Medtronic MiniMed, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number:…

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

ReCor Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2026

Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Pouch, UPC Code: 8 50005 60689 5

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

Tg Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 1, 2026

Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed. SKU #097908. Net wt. 1lb.…

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

Ajinomoto Foods North America Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2026

BD Alaris" System with Guardrails" Suite MX with Point of Care Unit

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers:…

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

I.T.S. GmbH

16 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K/B, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A,…

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

Merit Medical Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2026

SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES. INGREDIENTS: MUSTARD (DISTILLED…

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

Savannah Bee Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2026

Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;

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

Waldemar Link GmbH & Co. KG (Mfg Site)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2026

Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

DxC 700 AU, REF: B86444, B86446

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

Beckman Coulter Mishima K.K.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05

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

Exactech, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Artelon FlexBand Dynamic Matrix Ref: 31057

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

International Life Sciences

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2026

VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***)…

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

Palmetto Gourmet Foods Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2026

PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:…

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

Physio-Control, Inc.

FDA (openFDA device 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.

We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.

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.