State

Kansas product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48351–48375 of 79646

SevereFDA (Drugs)·D-0461-2017·2017-02-08
VistaPharm Recalls Nystatin Oral Suspension Due to Water Contamination
VistaPharm is recalling Nystatin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Product
Nystatin Oral Suspension, USP 500,000 Units/5 mL, a). 50 unit dose cups of 5 mL per case (NDC No. 66689-037-50), b). 100 unit dose cups of 5 mL per case (NDC 66689-037-99), Rx only, Manufactured by VistaPharm, Largo, FL 33771.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0457-2017·2017-02-08
VistaPharm Recalls Nystatin Oral Suspension Due to Potential Water Contamination
VistaPharm is recalling Nystatin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Product
Nystatin Oral Suspension, USP 100,000 units per mL, a) 2 fl. oz. (60 mL), 24 bottles per case (NDC 66689-008-02), b) 16 fl. oz. (237 mL), 12 bottles per case (NDC 66689-008-16), Rx only, Manufactured by VistaPharm, Largo, FL 33771
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V077000·2017-02-08
Mercedes-Benz Recalls 2017 GLE and GLS Models for Center Console Defect
Mercedes-Benz is recalling 2017 GLE and GLS models because the center console may unlatch in a crash, allowing objects to strike occupants.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLS550, GLE550E, AMG GLS63, AMG GLE63
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1397-2017·2017-02-08
Houdini Inc. Recalls Napa & Sonoma Valley Exclusive Basket #141 for Salmonella
Houdini Inc. is recalling 79 Napa & Sonoma Valley Exclusive Basket #141 units due to potential Salmonella contamination. The product was distributed nationwide, including Puerto Rico.
Product
Napa & Sonoma Valley Exclusive Basket #141
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0467-2017·2017-02-08
VistaPharm Recalls Methadone Hydrochloride Oral Concentrate Due to Water Contamination
VistaPharm is recalling 3,354 bottles of Methadone Hydrochloride Oral Concentrate because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Product
Methadone Hydrochloride Oral Concentrate, USP 5 mg/5 mL C-II, 500 mL, 6 bottles per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-711-16.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0449-2017·2017-02-08
Dr. Reddy's Recalls Flucanazole Tablets for Dissolution Failures
Dr. Reddy's Laboratories is recalling Flucanazole tablets because they failed dissolution and stability specifications.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1416-2017·2017-02-08
Houdini Inc. Recalls Classic Basket #6013 for Potential Salmonella Contamination
Houdini Inc. is recalling 66 Classic Basket #6013 units due to potential Salmonella contamination. The products were distributed nationwide, including Puerto Rico.
Product
The Classic Basket #6013
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1133-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers 275 units distributed worldwide.
Product
Intact Disposable Wands (part of the Intact System) 900-120: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0459-2017·2017-02-08
VistaPharm Recalls Metoclopramide Oral Solution Due to Potential Water Contamination
VistaPharm is recalling specific lots of Metoclopramide Oral Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Product
Metoclopramide Oral Solution, USP 10 mg/ 10 mL, 50 unit dose cups of 10 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-031-50.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·17V080000·2017-02-08
Mercedes-Benz Recalls 2017 Models for Air Bag Ignition Failure
Mercedes-Benz is recalling 2017 E300, E400, E550, GLA 250, and CLA250 vehicles because the pelvis or front passenger air bag inflator may fail to ignite in a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ E300, E400, GLA 250, CLA250
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1122-2017·2017-02-08
Mevion S250 Proton Therapy Units Recalled for Data Loss Error
Mevion Medical Systems is recalling two S250 Proton Radiation Therapy units because a software error can cause Delta corrections to be lost.
Product
MEVION S250-Proton Radiation Therapy Product Usage: Proton Radiation Therapy
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1128-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall affects 180 units distributed worldwide.
Product
Intact Disposable Wands (part of the Intact System) 777-112: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1127-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled Due to Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers 155 units distributed worldwide.
Product
Intact Disposable Wands (part of the Intact System) 900-112: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·17V075000·2017-02-08
Volkswagen Recalls 2017 Passat Vehicles Due to Brake Fluid Leak Risk
Volkswagen is recalling 2017 Passat vehicles because brake fluid may leak from line connections, potentially increasing stopping distance and crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN PASSAT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1124-2017·2017-02-08
Synthes Radial Head Prosthesis Recalled for Potential Stem Loosening
Synthes (USA) Products LLC is recalling 50,311 units of the Radial Head Prosthesis System because the radial stem may loosen post-operatively at the stem bone interface.
Product
Synthes Radial Head Prosthesis System, Surgical instrument motors and accessories Product Usage: Intended for primary and revision joint replacement of the radial head.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1135-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising product sterility.
Product
Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1111-2017·2017-02-08
Organ Preservation Solution Recalled for Potential Bacterial Contamination
Organ Recovery Systems is recalling SPS-1 Static Preservation Solution bags due to potential bacterial contamination.
Product
SPS-1, Static Preservation Solution [1 or 2 liter bags], Sterile; Organ Recovery Systems, One Pierce Place, Itasca, IL 60143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0450-2017·2017-02-08
Dr. Reddy's Recalls Flucanazole Tablets for Dissolution Failures
Dr. Reddy's is recalling Flucanazole tablets that failed dissolution and stability specifications. Patients should stop using the affected lots and consult their healthcare provider.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1121-2017·2017-02-08
Medtronic Strata II Valves Recalled for Pressure Discrepancies
Medtronic is recalling Strata II and Strata NSC valves used for hydrocephalus management due to reported discrepancies between the set pressure level and x-ray readings.
Product
Medtronic Strata II / Strata NSC Valves (includes Burr Hole and Lumbar Peritoneal. All Catalog Numbers. Strata-type valves are used in the management of hydrocephalus. The Strata II/Strata NSC valve is a shunt component designed to allow for continuous flow of cerebrospinal…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·17083·2017-02-08
La-Z-Boy Recalls Lift Chair Power Supplies Due to Shock Hazard
La-Z-Boy is recalling specific power supplies sold with lift chairs because the covers can crack and detach, exposing electrical components and posing a shock hazard.
Product
Power supplies sold with lift chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1120-2017·2017-02-08
Siemens IMMULITE PSA Kit Recall Due to Negative Bias Results
Siemens is recalling two lots of IMMULITE PSA kits because they produce negative bias results, potentially affecting prostate cancer screening accuracy.
Product
IMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LK3PS1, SMN 10706293 (US Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers for the quantitative measurement of prostate-specific antigen (PSA) in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1125-2017·2017-02-08
Covidien Nellcor SpO2 Forehead Sensor Recalled for Latex Labeling Error
FDA is recalling 7,453 units of the Covidien Nellcor SpO2 Forehead Sensor because the label incorrectly states the product is latex-free, while the headband contains latex.
Product
Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10; The Covidien Nellcor¿ Forehead SpO2Sensor, model RS10, is indicated for use when continuous non-invasive arterial oxygen saturation and pulse rate monitoring are required for patients weighing more than 40 kg.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1129-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling 252 Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The devices are used for breast tissue removal.
Product
Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1036-2017·2017-02-08
Olympus Vanta XRF Analyzers Recalled for LED Warning Light Failure
Olympus is recalling Vanta VCR and VMR XRF analyzers because the LED warning lights may fail to illuminate during X-ray emission.
Product
Olympus Scientific Solutions Americas Corporation (OSSA) VANTA¿ XRF Analyzer. Model Vanta VCR and Vanta VMR Analytical X-ray systems
Category
Medical Device
Distribution
22 states
HighFDA (Drugs)·D-0465-2017·2017-02-08
VistaPharm Recalls Methadone Hydrochloride Due to Potential Bacterial Contamination
VistaPharm is recalling Methadone Hydrochloride Oral Concentrate because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Product
METHADONE HYDROCHLORIDE — METHADONE HYDROCHLORIDE (METHADONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide