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.
Reported Jul 24, 2019
Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Sprouts Farmers Market Cut Leaf Spinach, Net Wt 16 Oz (1 lb), 453 g, Manufactured exclusively for Sprouts Farmers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sprout's Farmers Market
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 24, 2019
Wilton Chocolate decorator icing stiff consistency 16 oz plastic tub retail unit 6 or 12 retail units per wholesale unit
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Wilton Brands
FDA (openFDA food enforcement)
Reported Jul 17, 2019
Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Jul 17, 2019
Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2019
HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported Jul 10, 2019
WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.UNFI General Corporate
FDA (openFDA food enforcement)
Reported Jul 10, 2019
DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2019
Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks, such as general purpose pipetting and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2019
2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Horizon Cardiology Hemo
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Change Healthcare Israel Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dole Fresh Vegetables
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 5, 2019
Global Pride Rattan Shoots in Brine: 24 oz. glass jar UPC: 8855273023148 Erawan Enterprise Co. Ltd Bangkok, Thailand.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.U.S. Tov, Inc.
FDA (openFDA food enforcement)
Reported May 29, 2019
EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 29, 2019
Thio Med w/Dex, Hem, Vit K (5ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported May 29, 2019
Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
75 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Health Brands (Corporate Office)
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
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.