State

Kansas product recalls

73,827 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,822
Critical: 1,053
Severe: 1,486
Most recent: 2026-11-04

Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50751–50775 of 79649

ModerateFDA (Devices)·Z-2777-2016·2016-09-21
Integra Meshed Dermal Regeneration Template Recalled for Calculation Error
Integra LifeSciences is recalling 14 packages of Meshed Dermal Regeneration Template due to an incorrect calculation of peel strength test results.
Product
Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 in x 2in) Rx Only Meshed Integra¿ Dermal Regeneration Template, (Integra template) is a bilayer membrane system for skin replacement. The dermal replacement layer is made of a porous matrix of fibers of cross-linked…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1501-2016·2016-09-21
Amerisource Recalls bupropion Hydrochloride Tablets for Dissolution Failure
Amerisource Health Services is recalling 2,626 bottles of bupropion hydrochloride extended-release tablets due to failed dissolution specifications.
Product
buPROPion Hydrochloride Extended-Release Tablets, USP (XL), 300mg, 500-count bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories, NDC 68001-264-03
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2793-2016·2016-09-21
Siemens Syngo Plaza PACS Recall for Measurement Display Suffix
Siemens is recalling 101 Syngo Plaza PACS systems because a suffix on DICOM images may indicate that displayed measurements differ from actual values.
Product
Syngo Plaza picture archiving and communication system (PAC) (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2770-2016·2016-09-21
Sysmex Fluorocell PLT Reagent Recalled for Potential Low Platelet Results
Sysmex America Inc is recalling Fluorocell PLT reagent because it may produce falsely low platelet results on Sysmex XN-Series analyzers.
Product
Fluorocell PLT reagent, Catalog #CD994563 Fluorocell PLT is used to stain platelets in a diluted blood sample for the counting of platelets with the Sysmex XN-Series automated hematology analyzers
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2794-2016·2016-09-21
Siemens Syngo.Plaza VB 10 A PACS Recall for Measurement Suffix Display
Siemens is recalling 101 Syngo.Plaza VB 10 A image processing systems because a suffix on DICOM images may indicate that displayed measurement values differ from real values.
Product
Syngo.Plaza VB 10 A, image processing system (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2134-2016·2016-09-21
Pioneer Frozen Foods Recalls McGriddles Hot Cakes Due to Water Contamination
Pioneer Frozen Foods is recalling McGriddles Hot Cakes because rain water and condensate dripped onto the product, resulting in a high APC count.
Product
McGriddles Hot Cakes 192/1.75 oz packaged in brown cardboard box
Category
Food
Distribution
5 states
LowFDA (Devices)·Z-2804-2016·2016-09-21
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Calibrator Kit 31
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 31, Lot 3155, because an incorrect value on the Assay Data Disks prevents successful calibration of the HbA1c assay.
Product
The VITROS¿ Chemistry Products Calibrator Kit 31, Lot 3155 used in conjunction with: VITROS¿ Chemistry Products HbA1c Reagent Kit, Generation 6 (GEN 6) and Assay Data Disk (ADD), Data Release Versions (DRV) 5873, 5874, 5875, or 5876, is used to calibrate the VITROS 5,1 FS…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2779-2016·2016-09-21
Biomerieux Recalls VIDAS NT-pro-BNP Kits Due to Packaging Error
Biomerieux is recalling 229 VIDAS NT-pro-BNP kits because they contain the incorrect number of control vials.
Product
VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2778-2016·2016-09-21
Alere LDX Optical Check Cassettes Recalled for Incorrect Expiration Date
Alere San Diego, Inc. is recalling LDX Optical Check Cassettes because the expiration date on the magnetic strip does not match the labeled date.
Product
LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Cassette in box with foam insert. The cassette is used to check the optics system of the LDX analyzer. Product Usage: The Optics Check Cassette is used to check the optics system of the Alere Cholestech…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V678000·2016-09-20
New Flyer Recalls 2016 XN60 and XN40 Buses for CNG Defect
New Flyer is recalling 38 model year 2016 XN60 and XN40 transit buses because a pressure relief device may fracture, releasing high-pressure gas and increasing fire risk.
Product
NEW FLYER — NEW FLYER XN60, XN40
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V679000·2016-09-20
Ducati Recalls XDiavel Motorcycles for Loose Final Drive Pulley Nut
Ducati is recalling 2016-2017 XDiavel motorcycles because a loose final drive pulley nut may cause loss of power to the rear wheel, increasing crash risk.
Product
DUCATI — DUCATI XDIAVEL
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16E073000·2016-09-20
Porsche Brake Fluid Recall Due to Missing DOT 4 Labeling
Porsche is recalling specific 1L and 30L brake fluid containers manufactured between September 2015 and August 2016 because they lack the required 'DOT 4' label, posing a risk of incompatible fluid use.
Product
SERVICE BRAKES, HYDRAULIC:FLUID recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V680000·2016-09-20
Porsche Recalls 2017 Macan Models Due to Front Suspension Defect
Porsche is recalling 2017 Macan models because front anti-rollbar links may move out of position, causing oversteer and increasing crash risk.
Product
PORSCHE — PORSCHE MACAN
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16267·2016-09-20
Denon Recalls HEOS 1 Go Pack Battery Packs for Fire and Burn Hazards
Denon is recalling HEOS 1 Go Pack rechargeable battery packs because they can overheat, posing fire and burn hazards. No injuries have been reported.
Product
HEOS 1 Go Pack rechargeable battery packs
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·16V674000·2016-09-19
Utility Recalls 2015-2017 Flatbed Trailers Due to Tarping System Defect
Utility Trailer Manufacturing Company is recalling 2015-2017 Flatbed trailers because the rear aerodynamic device may detach, creating a road hazard.
Product
UTILITY — UTILITY FLATBED TRAILERS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V675000·2016-09-19
Mitsubishi Recalls 2017 Mirage Vehicles for Headlight Adjustment Defect
Mitsubishi is recalling 2017 Mirage vehicles with HID headlamps because the horizontal adjustment clips may not be secured, potentially reducing visibility or blinding oncoming drivers.
Product
MITSUBISHI — MITSUBISHI MIRAGE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V676000·2016-09-19
Spartan Emergency Response Vehicles Recalled for Power Steering Pump Defect
Spartan Motors is recalling 2010-2017 K3, Gladiator, and Metrostar chassis due to a power steering pump defect that may cause intermittent loss of steering assist.
Product
SPARTAN — SPARTAN K3, GLADIATOR, METROSTAR
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·083-2016·2016-09-17
Gallo Meats Recalls Sausage, Beef, and Lamb Products Lacking Federal Inspection
Gallo Meats LLC is recalling approximately 82 pounds of sausage, beef, and lamb products produced without federal inspection. The hot Italian sausage may also contain undeclared allergens.
Product
Gallo Meats LLC. Recalls Sausage, Beef and Lamb Products Produced Without Benefit of Inspection
Category
Food
Distribution
Distributed nationwide
SevereUSDA FSIS·081-2016·2016-09-16
Tucson Tamale Wholesale Recalls Beef Tamales Lacking Federal Inspection
Tucson Tamale Wholesale Company is recalling 915 pounds of beef tamales because the meat was produced without federal inspection. No illnesses have been reported.
Product
Tucson Tamale Wholesale Company LLC — Tucson Tamale Wholesale Company, LLC Recalls Beef Tamale Products Containing Meat Produced Without Benefit of Federal Inspection
Category
Food
Distribution
Distributed nationwide
HighNHTSA·16V672000·2016-09-16
Toyota Recalls 2016 Prius Vehicles Due to Air Bag Inflation Error
Toyota is recalling 7,817 model year 2016 Prius vehicles because a manufacturing error may cause the front passenger air bag to partially inflate unintentionally.
Product
TOYOTA — TOYOTA PRIUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V671000·2016-09-16
Jayco Recalls 2017 Octane Travel Trailers for Incorrect Tire Labels
Jayco is recalling 2017 Octane Super Lite travel trailers because incorrect tire labels may lead to over-inflation and sudden tire failure.
Product
JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER OCTANE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V673000·2016-09-16
Forest River Recalls 2017 Salem and Wildwood Trailers for Incorrect Tire Placards
Forest River is recalling 2017 Salem and Wildwood recreational trailers because the Federal Placard lists incorrect tire and rim specifications, which may lead to under-inflation and increased crash risk.
Product
FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·16264·2016-09-15
Polaris Recalls Ranger 900 Vehicles Due to Fire and Burn Hazards
Polaris is recalling about 42,500 model year 2014 Ranger 900 vehicles because a heat shield can fall off, creating fire and burn risks.
Product
Polaris Ranger 900 recreational off-highway vehicles (ROVs)
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·16265·2016-09-15
GE Profile Top-Loading Clothes Washers Recalled for Fire Hazard
GE Appliances is recalling about 222,000 Profile top-loading clothes washers because an electrical component can overheat and cause a fire.
Product
GE Profile™ top-loading clothes washers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·16266·2016-09-15
Samsung Recalls Galaxy Note7 Smartphones Due to Fire and Burn Hazards
Samsung is recalling Galaxy Note7 smartphones sold before September 15, 2016, because the lithium-ion battery can overheat and catch fire, posing a burn hazard.
Product
Samsung Galaxy Note7 smartphones sold prior to September 15, 2016
Category
Consumer Product
Distribution
Distributed nationwide