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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 Dec 24, 2025

InPen App, Model/CFN Number: MMT-8061 (Android Users)

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

Myosa for Kids KS1 REF MyOSAKS1_Sb/Sp/Mb/Mp/Lb/Lc KS2 REF MyOSAKS2_Sb/Sc/Mb/Mc/Mp/Lb/Lc Myosa for Kids is a mouthguard…

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

Myofunctional Research Company USA

FDA (openFDA device enforcement)

Food

Reported Dec 17, 2025

UPC 8 10248 03165 6 YELLOW Peaches PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654…

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

Moonlight Packing Corporation

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 17, 2025

Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number:…

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

Orthofix U.S. LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 10, 2025

Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE…

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

Accriva Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2025

Costco Item# 19927 Kirkland Signature Caesar Salad, refrigerated, packaged in clear plastic clamshell container. The…

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

Costco Wholesale Corporation

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Low-moisture part-skim mozzarella shredded cheese, individually packaged in a plastic bag, as: 1) Always Save -…

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

Great Lakes Cheese Co. Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Lava Bun with Green Tea Flavor bright lime green packaging (Frozen) Unsalted butter and cream are listed in the…

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

Prime Food Processing LLC.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Italian Salad Dressing; Net 1 GAL (3.78L) SKU: 7 67367 00518 4 Creamy Poblano Avocado Ranch Dressing and Dip; Net…

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

Ventura Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/…

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

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

FoundationOne CDx (F1CDx), RAL-0003 version 31.0

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

Foundation Medicine, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

CareLink Clinic, REF: MMT-7350

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;

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

Philips Medical Systems Nederland B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest…

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

Cellavision AB

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Clot Activator Model/Catalog Number: 455071P Product…

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A,…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult…

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

Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US,…

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

Thoratec LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 19, 2025

Peach Salsa - $5.99-16 oz 639123940636 packaged in clear plastic clamshells Sell by 11/3/2025 Sell by 11/4/2025

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

Jfe Franchising Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 19, 2025

Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers:…

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

Medline Industries, LP

20 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 19, 2025

Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 90, Dose: 2 Capsules. Product Sku:…

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

Professional Botanicals, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 19, 2025

Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The…

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

Shimadzu Corporation Medical Systems Division

FDA (openFDA device enforcement)

Medical devices

Reported Nov 12, 2025

SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent, REF: 969706

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

Beckman Coulter Inc.

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.