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 Apr 30, 2025

Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported Apr 30, 2025

Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack;…

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

S Martinelli & Company

FDA (openFDA food enforcement)

Food

Reported Apr 30, 2025

Walker's Wine Juice Pumpkin Juice 2.5, 5, 30, 60, 275 gallon bulk containers

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

Walker's Fruit Basket and Press House

FDA (openFDA food enforcement)

Medical devices

Reported Apr 23, 2025

Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 198 Software Version: N/A Product…

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

Avanos Medical, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196,…

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

Bard Access Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, REF: 1145-00; MEDBANK…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 23, 2025

Farmer House Preserve Olive Strips

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

Lins Waha International Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 23, 2025

Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.

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

Philips North America LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 23, 2025

Trader Joe's Hot Honey Mustard Dressing (SKU #80152), packaged in glass bottle with tamper overwrap on plastic cap, net…

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

Reser's Fine Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 23, 2025

HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with…

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

Thoratec LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200…

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

ZOLL Circulation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 16, 2025

BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated…

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 16, 2025

Lillie's Q Buffalo Wing Sauce. Net wt. 13.5 oz, UPC 810069510972, Case label: Lillie's Q Buffalo Wing Sauce, Item #…

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

Old World Spices & Seasoning, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 9, 2025

BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Food

Reported Apr 9, 2025

Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a…

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

Nestle-USA, Inc. (Corporate Office)

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 9, 2025

Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version:…

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Meat & poultry

Reported Apr 5, 2025

Johnsonville, LLC, Recalls Cheddar Bratwurst Product Due to Possible Foreign Matter Contamination

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

Momence Real Estate

USDA FSIS

Medical devices

Reported Apr 2, 2025

CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of…

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

Calyxo, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 2, 2025

COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ…

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

Massimo Zanetti Beverage USA

FDA (openFDA food enforcement)

Medical devices

Reported Apr 2, 2025

CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital System Model CM3100 -CardioMEMS Backend Web…

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

St. Jude Medical

FDA (openFDA device enforcement)

Food

Reported Apr 2, 2025

DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING…

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

U.S. Tov, Inc. dba U.S. Trading Company

FDA (openFDA food enforcement)

Medical devices

Reported Apr 2, 2025

NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF:…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.

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

FUJIFILM Healthcare Americas Corporation

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.