State

Kansas product recalls

73,722 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,821
Critical: 1,053
Severe: 1,485
Most recent: 2026-10-28

Of the 5,821 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 1,485 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28801–28825 of 79543

SevereFDA (Drugs)·D-0103-2021·2020-12-02
Paroex Oral Rinse Recalled for Burkholderia lata Contamination
Sunstar Americas is recalling Paroex Oral Rinse due to microbial contamination with Burkholderia lata. The recall covers specific lots distributed nationwide.
Product
Paroex (chlorhexidine gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only, packaged in: a) 1 pint (473 mL) NDC 52376-021-02; b) 4 fl oz (118 mL) NDC 52376-021-04, Sunstar Americas, Inc.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0484-2021·2020-12-02
Hill-Rom Recalls Life2000 Ventilation Systems Due to Fire Risk
Hill-Rom is recalling 67 Life2000 Ventilation Systems because they pose a risk of fire under certain conditions. The devices are used in home and institutional settings.
Product
Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage: use in home and institutional settings and is not intended for ambulance or air transport.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V750000·2020-12-02
Kia Recalls 294,756 Vehicles for Engine Compartment Fire Risk
Kia is recalling 294,756 vehicles from 2011-2015 due to a risk of engine compartment fire while driving. Dealers will inspect for leaks and update software.
Product
KIA — KIA FORTE KOUP, SOUL, FORTE, SORENTO
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0491-2021·2020-12-02
FDA Recalls Geistlich Bio-Oss Pen Due to Granule Expulsion Risk
Geistlich Pharma North America is recalling Geistlich Bio-Oss Pen units because granules may be expelled all at once, posing a risk of tissue injury.
Product
Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone mineral for filling of bone defects in maxillofacial surgery, implantology, and periodontology. Product Number: 20116
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V749000·2020-12-02
Audi 2021 A6, Q7, RS6, and RS7 Crash Sensor Electrical Defect
Volkswagen Group of America (Audi) is recalling 2021 Audi A6, Q7, RS6, and RS7 vehicles. An electrical connector can detach from door crash sensors, potentially delaying restraint system activation during side-impact crashes.
Product
AUDI — AUDI RS 6 AVANT, RS 7, A6, Q7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0126-2021·2020-12-02
Natural Grocers Organic Elderberries Recalled for Salmonella Contamination Risk
Natural Grocers is recalling 4 oz. bags of Whole Organic Elderberries due to potential Salmonella contamination. Consumers should check their pantry for the specific UPC and lot codes.
Product
Natural Grocers, Elderberries Whole Organic, 4 oz. (113g), plastic bag, UPC 0-0082-00304-3
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-0483-2021·2020-12-02
Bayer Recalls MEDRAD Stellant FLEX Syringe Kits Due to Cracks
Bayer Medical Care is recalling specific lots of MEDRAD Stellant FLEX 150 mL syringe kits because they may have holes or cracks that allow fluid to leak.
Product
Brand Name: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic Syringe Catalog/REF Number: FLEXD-150-SCS Description: 2 - 150 mL FLEX syringes, 1 large saline spike, 1 small contrast spike, patient t-connector tubing & prime tube. Catalog/REF Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0482-2021·2020-12-02
ViewRay MRIdian Linac System Recalled for Potential Burn Injury Risk
Viewray, Inc. is recalling 35 ViewRay MRIdian Linac Systems because receive coil components may reach elevated temperatures, posing a risk of burn injury to patients or users.
Product
ViewRay MRIdian Linac System: Model No. 20000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60 Hz, Rated Input in Amperes - 210 A, UDI. The MRIdian system and the MRIdian Linac system, with magnetic resonance imaging capabilities, is intended to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0492-2021·2020-12-02
Geistlich Bio-Oss Pen Recalled Due to Granule Expulsion Risk
Geistlich Pharma North America is recalling Geistlich Bio-Oss Pen 1-2mm 0.5g units because granules may be expelled all at once, posing a risk of tissue injury.
Product
Geistlich Bio-Oss Pen 1-2mm 0.5g - Product Usage: natural bone mineral for filling of bone defects in maxillofacial surgery, implantology, and periodontology. Product Number: 20126
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21039·2020-12-02
ADCO Recalls Sure Scents Candles Due to Fire and Burn Hazards
ADCO is recalling Sure Scents 2-1 Peaceful Stream/Moonlit Waves candles sold at Dollar Tree because high flames can ignite wax or break glass, posing fire and burn risks.
Product
Sure Scents 2-1 Peaceful Stream/Moonlit Waves Candles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0109-2021·2020-12-02
Eywa Pharma Recalls Levetiracetam Tablets Due to Foreign Tablet Presence
Eywa Pharma Inc. is recalling 500 mg Levetiracetam tablets because a 1000 mg tablet was found in a 500 mg bottle.
Product
Levetiracetam Tablets, USP 500 mg, packaged in 120-count bottle, Rx only, Manufactured by: VKT Pharma Private Limited Srikakulam, India - 532 409, Manufactured for: Eywa Pharma Inc. 2 Research Way, Floor 3 Princeton, NJ 08540, NDC 71930-063-52
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0490-2021·2020-12-02
FDA Recalls Geistlich Bio-Oss Pen Due to Granule Expulsion Risk
Geistlich Pharma North America is recalling Geistlich Bio-Oss Pen units because granules may be expelled all at once, posing a risk of tissue injury.
Product
Geistlich Bio-Oss Pen 0.25-1mm 0.25g - Product Usage: natural bone mineral for filling of bone defects in maxillofacial surgery, implantology, and periodontology. Product Number: 20115
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21040·2020-12-02
Huffy Recalls Torex Ride-on Toy UTVs Due to Injury Hazard
Huffy is recalling Torex 24V ride-on toy UTVs sold at Walmart because the toys can unexpectedly move when the battery is connected, posing an injury hazard.
Product
Huffy Torex 24V ride-on toy UTVs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0488-2021·2020-12-02
Coloplast Titan Pump Recall for Potential Device Fracture
Coloplast is recalling 8,962 Titan Pump units due to a potential increased occurrence of pump fracture over the device's lifetime.
Product
Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are considered to be candidates for implantation of a penile prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0478-2021·2020-12-02
RayStation software recall for potential incorrect treatment plan references
RaySearch Laboratories is recalling RayStation software because missing data may cause treatment plans to reference incorrect regions or points of interest.
Product
RayStation standalone software treatment planning system, Model No. 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0, 9.1, 9.2, 10.0 - Product Usage: RayStation is a software system for radiation therapy and medical oncology. Based on user input, RayStation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0485-2021·2020-12-02
Mevion Proton Radiation Treatment System Recalled for Screen Display Failure
Mevion Medical Systems is recalling eight MEVION S250 and S250i proton radiation treatment systems because treatment beam information may disappear from the console screen while the beam continues to deliver.
Product
MEVION S250i, MEVION S250; Proton Radiation Treatment System - Product Usage: intended to deliver proton radiation treatment to patients with localized tumors or any other conditions susceptible to treatment by radiation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0489-2021·2020-12-02
Intuitive Surgical Recalls ION Fully Articulating Catheters Due to Tip Ring Risk
Intuitive Surgical is recalling 454 ION Fully Articulating Catheters because the distal tip ring may become dislodged during use.
Product
Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully Articulating Catheter within the lung to a planned path in order to sample a target. User Manual: ION Endoluminal System, System, Instruments, and Accessories User…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0481-2021·2020-12-02
ViewRay MRIdian System Recalled for Potential Burn Injury Risk
ViewRay is recalling three MRIdian systems because receive coil components may reach elevated temperatures, posing a potential risk of burn injury to patients or users.
Product
ViewRay MRIdian System: Model No. 10000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60 Hz, Rated Input in Amperes - 210 A, UDI. The MRIdian system and the MRIdian Linac system, with magnetic resonance imaging capabilities, is intended to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0104-2021·2020-12-02
Jubilant Cadista Recalls Clomipramine Hydrochloride Capsules Due to Specification Failure
Jubilant Cadista Pharmaceuticals is recalling 4,416 bottles of clomipramine hydrochloride capsules because they failed tablet/capsule specifications.
Product
clomiPRAMINE Hydrochloride Capsules USP, 50 mg, 30-count bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD NDC 59746-711-30
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0493-2021·2020-12-02
Medtronic Cardioblate CryoFlex Surgical Ablation Probe Recalled for Seal Defects
Medtronic is recalling 37 units of the Cardioblate CryoFlex Surgical Ablation Probe due to potential defects in the sterile barrier pouch seals.
Product
Cardioblate CryoFlex, Surgical Ablation Probe, Model Number 60SF2, PROBE 60SF2 CRYOFLEX 10CM 26L - Product Usage: is a single use, disposable cryoprobe that is designed for use with the CryoFlex Surgical Ablation System. The probe has an integrated thermocouple for monitoring…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0496-2021·2020-12-02
Medtronic Recalls CryoFlex Surgical Ablation Probes Due to Seal Defects
Medtronic is recalling 3 units of Cardioblate CryoFlex Surgical Ablation Probes because of a potential defect in the sterile barrier pouch seals.
Product
Cardioblate CryoFlex, Surgical Ablation Probe, Model Number 60CM1, CLAMP 60CM1 CRYOFLEX PROBE 26L - is a single use, disposable cryoprobe that is designed for use with the CryoFlex Surgical Ablation System. The probe has an integrated thermocouple for monitoring temperature at…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0494-2021·2020-12-02
Medtronic Cardioblate CryoFlex Surgical Ablation Probe Recall for Seal Defects
Medtronic is recalling 57 units of the Cardioblate CryoFlex Surgical Ablation Probe due to a potential defect in the sterile barrier pouch seals.
Product
Cardioblate CryoFlex, Surgical Ablation Probe, Model Number 60SF3, PROBE 60SF3 CRYOFLEX 10-S 26L - is a single use, disposable cryoprobe that is designed for use with the CryoFlex Surgical Ablation System. The probe has an integrated thermocouple for monitoring temperature at…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0110-2021·2020-12-02
Teligent Recalls Subpotent Triamcinolone Acetonide Lotion
Teligent Pharma is recalling one lot of Triamcinolone Acetonide Lotion because it does not meet assay results.
Product
Triamcinolone Acetonide Lotion USP, 0.025%, 60 mL (60 grams) bottle, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-010-59
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0477-2021·2020-12-02
Luminex Recalls Verigene Processor SP Due to Unapproved Test Fixtures
Luminex is recalling 2,838 Verigene Processor SP units because field service engineers used unapproved test fixtures to calibrate the devices.
Product
Verigene Processor SP, Model Numbers 10-0000-07 and 10-0000-07R. Used with assay Luminex, VERIGENE Gram-Negative Blood Culture Nucleic Acid Test, BC-GN, IVD - Product Usage: IVD sample processor, which utilizes a single-use disposable test consumable and a self-contained…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0486-2021·2020-12-02
Advanced Bionics Recalls Mislabelled PowerCel 230 Cochlear Implant Batteries
Advanced Bionics is recalling 53 PowerCel 230 batteries for cochlear implants because they may be mislabeled with incorrect battery life information.
Product
AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da CI Q90 Sound Processor (CI-5280), Na¿da CI Q70 Sound Processor (CI-5245) and Na¿da CI Q30 Sound Processor (CI-5260) for cochlear implant.
Category
Medical Device
Distribution
Distributed nationwide