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 48,759 notices were distributed nationwide, so they reach Kansas too — those are in the archive.
Reported Jan 31, 2024
TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Atrial Fibrillation Division, Inc.
FDA (openFDA device enforcement)
Reported Jan 24, 2024
PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Ministry of Snacks Sweet and Savory Collection #8700
High riskUsing this product could cause serious injury, illness or death — stop using it now.Houdini Inc.
FDA (openFDA food enforcement)
Reported Jan 24, 2024
High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123
High riskUsing this product could cause serious injury, illness or death — stop using it now.Percussionaire Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phase Scientific International Limited
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Chicken Broth sold under Chef's Cupboard, 32oz Chicken Stock, UPC: 4099100067699, carton Gold Emblem, 32oz Chicken…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TreeHouse Foods, Inc.
14 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 17, 2024
Alinity i Processing Module REF 03R65-01 The Alinity i Processing Module is a fully automated immunoassay analyzer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
CD11b APC: ASR, REF: 340936, and CE, REF: 333143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Jan 17, 2024
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnostic test…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies) packaged in 11.85oz cardboard candy box with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eban's Bakehouse LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 17, 2024
Incisive CT, model 728143 & 728144 running Software Version 5.0.0.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare (Suzhou) Co., Ltd.
FDA (openFDA device enforcement)
Reported Jan 17, 2024
CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Townsend Design
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 10, 2024
Merit Maestro Microcatheter, Reference Numbers: 28MC2111045/B, 28MC21110ST/B, 28MC2113045/B, 28MC21130SN/CNB,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 10, 2024
External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 10, 2024
Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Respironics, Inc.
FDA (openFDA device enforcement)
Reported Jan 3, 2024
Alinity ci-series System Control Module, REF: 03R70-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jan 3, 2024
RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320, Low Profile Primary Guide is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN Sapphire, Model CD Sapphire, list number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Injection Needle, REF: 25207
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2023
0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nurse Assist, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2023
ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Right Angle Cutting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Dec 27, 2023
AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, 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.