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 Jan 8, 2025

Whole and Cut Cucumbers packaged in the following sizes: 1. Peak Cucumber Item 08027, 24 count. Product of Mexico. 2.…

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

Russ Davis Wholesale

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 8, 2025

Sprout Gyro Family Kit, net wt. 1.750 lb (794 g), food, perishable, plastic tray, 28oz, U UPC 20594800000.

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

Sprouts Farmers Market

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2025

The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming…

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

20/30 INDEFLATOR, REF: 1000184, for use during cardiovascular procedures in conjunction with interventional devices…

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

Abbott Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2025

BORSARI Food Company Incorporated; BLOODY MARY MIX ; 32 FL. OZ; INGREDIENTS: Tomato juice, corn syrup, non-fat milk…

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

Borsari Food Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2025

EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706

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

Encore Medical, LP

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…

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

Straight Smile, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2024

Fabalish Inc. , Kickin, Carrot Falafel , 10oz , Cardboard tray inside plastic film inside cardboard box, individual…

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

Fabalish,

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2024

OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging…

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

GE OEC Medical Systems, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2024

Bakestone Brothers Pita Bread, 6 White Pita. Net Wt. 11.4 oz(325g) UPC 0 57391-00001 0. Manufactured by PBF pita Bread…

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

Rise Baking Company, LLC dba The New French Bakery Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2024

Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2024

BD Pyxis MedStation ES, REF: 323

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2024

DKS Disposable Kerrison System, Catalog Number DKS-63030, instrument sets that come in two sizes (3.75mm and 6.35mm)…

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

Folsom Metal Products, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2024

"***SUPER***BRAND***DRIED CINNAMON POWDER***Net Wt: 4oz(113g)***PRODUCT OF CHINA***DISTRIBUTOR: IHA BEVERAGE COMMERCE,…

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

Kim-Seng Company

FDA (openFDA food enforcement)

Food

Reported Dec 18, 2024

Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton

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

Tipp Distributors, Inc. dba Novamex

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)

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

Cartiva, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2024

EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

AMS Artificial Urinary Sphincter Control Pump

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

4.5 x 180 mm REF 28208BKS Aggressive Cutter, sterile, 6x 3.5 x 70 mm REF 28206CBS Full Radius Resector, sterile, 6x 5.5…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an…

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

Kci USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively measures C-reactive protein (CRP)…

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue…

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

Ethicon, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 27, 2024

Douglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle. UPC # 10539 97452, Lot Numbers ,50335944…

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

Nestle Product Technology Center - Nestle Health Science

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.