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 Oct 8, 2025

NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NES Reprocessed…

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

Northeast Scientific Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 8, 2025

Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as 12pk. Outer case label reads as , "*** Lipton Green Tea Citrus…

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

Pepsico Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 8, 2025

IMPLANT EPIKUT PLUS MT16 3,5X10,0MM, REF: ILM 3510N; IMPLANT EPIKUT PLUS MT16 3.8X11.5MM, REF: ILM 3511N; IMPLANT…

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

S.I.N. Implant System Ltda

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

GORE ACUSEAL Vascular Graft, REF: ECH050020J, ECH050020W, ECH050050J, ECH050050W, ECH060010A, ECH060020A, ECH060020J,…

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

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2025

STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device, SFX SPI PDS+ BI VIO 14X14IN(36X36CM) USP1(M4)…

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

Ethicon, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 1, 2025

GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET WT 5.25 OZ (149g) INGREDIENTS: GOODLES SPIRALS…

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

Gooder Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 24, 2025

AquaStar Cocktail Shrimp, 4oz. shrimp/2oz. cocktail sauce. Each case consists of 6x6 oz packages, UPC 19434612191.…

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

Admiralty Island Fisheries Inc. dba AquaStar (USA) Corp.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 24, 2025

Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number: 92328632-09

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2025

Exactech Equinoxe, Reverse Shoulder Humeral Liners, REF: 320-38-00,145-DEG PE 38MM HUM LINER +0/ 320-38-03,145-DEG PE…

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)

Food

Reported Sep 24, 2025

FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS SUPPORTS TENDONS & MUSSCLES PROMOTES HEALTH…

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

Hi-Tech Pharmaceuticals Inc.

15 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 24, 2025

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+…

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

Max Mobility LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2025

Pinnacle Radiation Therapy Planning System: Multimodality Simulation Workspace 18.0.5 Model 870258 UDI code:…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 17, 2025

Peanut rounds 2.25 oz and 3 oz

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

Anderson Candy Company, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2025

CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x 100 um, SterileEO, RX…

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

Corneat Vision, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311…

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

Encore Medical, LP

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 17, 2025

Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with…

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

M.O.M Enterprises, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2025

QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SC

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿…

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

Integra LifeSciences Corp. (NeuroSciences)

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2025

Lemon Meringue Pie, 8" round. Net Wt. 27 OZ; Refrigerate after opening Item Code 31811; UPC: 8 85523 31811 1;Jessie's…

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

Jessie Lord Bakery, LLC

FDA (openFDA food enforcement)

Food

Reported Sep 10, 2025

Salad Kit labeled as follows: Taylor FARMS Honey Balsamic SALAD KIT, NET WT. 8.3 OZ (235g), INGREDIENTS: HONEY BALSAMIC…

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

Taylor Farms Retail, Inc.

FDA (openFDA food enforcement)

Food

Reported Sep 3, 2025

Chocolate Chip Cookie Dough ice cream cartons with a Moo-llennium Crunch lid. Packaging contains Moo-llennium crunch.…

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

Blue Bell Creameries, LP

FDA (openFDA food enforcement)

Drugs

Reported Sep 3, 2025

Enoxaparin Sodium Injection, USP, 30 mg/0.3 mL, packaged in 0.3 mL prefilled syringes further packaged in bags of 5…

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

Cardinal Health Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 3, 2025

BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis"…

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

CareFusion 303, 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.

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.