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.

28776–28800 of 79543

ModerateFDA (Devices)·Z-0515-2021·2020-12-09
Capnostream 35 Portable Respiratory Monitor Recalled for False Temperature Display
Covidien LLC is recalling 3,217 Capnostream 35 Portable Respiratory Monitors because they may display a false 'Temperature Exceeds Limits' message and shut down without an alarm.
Product
Capnostream 35 Portable Respiratory Monitor, Product numbers PM35MN02, PM35MN01, PM35MN05, DLPM35MN02 - Product Usage: use during both no motion and motion conditions and for patients who are well or poorly perfused.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0112-2021·2020-12-09
Golden State Medical Supply Recalls Aripiprazole Tablets for Dissolution Concerns
Golden State Medical Supply is recalling Aripiprazole 15 mg tablets due to potential out-of-specification dissolution limits.
Product
ARIPIPRAZOLE TABLETS, 15 mg, 30-count. bottles, Rx Only, GSMS Incorporated, Manufactured by: Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS, Incorporated, Camarillo, CA 93012 USA, NDC #60429-449-30
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0511-2021·2020-12-09
ICU Medical Recalls IV Administration Sets with Incorrect Filter Assemblies
ICU Medical is recalling 1,100 units of smallbore IV administration sets due to incorrect filter assemblies. The products were distributed nationwide.
Product
REF MC330209 6' (15 cm) Appx 0.09 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 0.2 Micron Filter, 1.2 Micron Filter, 3 Clamps (Blue, Yellow, White), Rotating Luer - Product Usage: The intravascular administration set is a single use, sterile, non-pyrogenic device, which…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0522-2021·2020-12-09
Chromsystems Recalls MassChrom Cortisol Saliva Control Level I Vials
Chromsystems is recalling 880 vials of MassChrom Cortisol, Cortisone Saliva Control Level I because the control lots may not meet stability criteria, potentially causing increased patient results.
Product
MassChrom Cortisol, Cortisone Saliva Control Level I, Order No. 0349 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0519-2021·2020-12-09
Bausch & Lomb Recalls Toric Intraocular Lenses Due to Missing Axis Marks
Bausch & Lomb is recalling 31 MX60ET toric intraocular lenses because they may be missing toric axis marks, which are necessary for proper surgical placement.
Product
MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is intended for placement in the capsular bag.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0114-2021·2020-12-09
Harvard Drug Group Recalls Aripiprazole Tablets for Dissolution Failure
The Harvard Drug Group is recalling 841 cartons of Aripiprazole Tablets, 15 mg, because the product failed to meet dissolution specifications.
Product
Aripiprazole Tablets, USP, 15 mg, 30 tablets per unit dose carton, Rx Only, Manufactured by: Apotex, Inc, Toronto, Ontario Canada M9L 1T9, Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 USA, NDC 0904-6512-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0524-2021·2020-12-09
ROi CPS Recalls Labor and Delivery Kits Due to Labeling Error
ROi CPS LLC is recalling 220 labor and delivery kits because of an incorrect expiration date on the label.
Product
Regard - Product Usage: Obstetric Gynecologic specialized manual instrument. Labor and delivery kits.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0508-2021·2020-12-09
BD Ultra-Fine Pen Needles Recalled for Incorrect US Labeling
Becton Dickinson is recalling 2.8 million BD Ultra-Fine Pen Needles because US cartons are missing specific compatibility information.
Product
BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for parenteral administration of a drug from a cartridge contained in a drug pen injector Catalog Number: 320122
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0521-2021·2020-12-09
Chromsystems Saliva Calibrator Set Recalled for Stability Issues
Chromsystems is recalling 6PLUS1 Multilevel Saliva Calibrator Sets because they may not meet stability criteria, potentially causing increased cortisone results in patient samples.
Product
6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva, Order No. 73039 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0523-2021·2020-12-09
Chromsystems Recalls MassChrom Cortisol and Cortisone Saliva Control Level II Kits
Chromsystems is recalling MassChrom Cortisol, Cortisone Saliva Control Level II kits because control lots may not meet stability criteria, potentially causing increased results for patient cortisone samples.
Product
MassChrom Cortisol, Cortisone Saliva Control Level II, Order No. 0350 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0512-2021·2020-12-09
Talladium Luminesse ML PMMA Milling Blank Recall for Incorrect Label
Talladium Inc is recalling 10 units of Luminesse ML PMMA milling blanks due to incorrect labels that may cause compatibility issues with milling machines.
Product
Luminesse ML PMMA, 98x20mm, REF: 5336-B1 - Product Usage: used as a milling blank in the fabrication of provisional crowns and bridges. All blanks are solely used by a Trained Dental Technician or on the order of a dental professional.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0119-2021·2020-12-09
Teligent Pharma Recalls Clobetasol Propionate Ointment Due to Potency Issues
Teligent Pharma is recalling Clobetasol Propionate Ointment 0.05% because some tubes have superpotent or subpotent assay results.
Product
Clobetasol Propionate Ointment USP 0.05%, Net Wt. 50 grams, Rx Only, Teligent Pharma. Inc. Buena, NJ 08310 NDC 52565-039-60
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0115-2021·2020-12-09
InvaTech Recalls Levocetirizine Dihydrochloride Tablets Due to Stability Failure
InvaTech Pharma Solutions is recalling specific lots of Levocetirizine Dihydrochloride Tablets 5 mg because one lot failed stability testing.
Product
Levocetirizine Dihydrochloride Tablets, USP, 5 mg 30-count bottle, Rx Only, Distributed by: Marlex Pharmceuticals, Inc. New Castle, DE 19720. NDC 10135-0639-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V759000·2020-12-08
Nissan Recalls 2020 Titan Trucks Due to Engine Wiring Fire Risk
Nissan is recalling 2020 Titan and Titan XD trucks because an exposed wire in the engine harness could cause an electrical short, leading to engine stall or fire.
Product
NISSAN — NISSAN TITAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V757000·2020-12-08
Grand Design Recalls 2020 Transcend Trailers Due to Gas Leak Risk
Grand Design is recalling 2020 Transcend recreational trailers because a gas leak at the cook stove joint may increase the risk of fire.
Product
GRAND DESIGN — GRAND DESIGN TRANSCEND
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V756000·2020-12-08
2019 Mercedes-Benz Sprinter Vehicles Recalled for Inaccurate Operator's Manual
Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter vehicles because the provided operator's manual may contain inaccurate or incomplete safety information.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 4500, SPRINTER 3500, SPRINTER 1500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V758000·2020-12-08
McNeilus Recalls 2020 Bridgemaster V Mixers Due to Missing Axle Information
McNeilus is recalling 2020 Bridgemaster V Mixer trucks because the required pusher axle operating position is missing from the information plate, increasing crash risk.
Product
MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V755000·2020-12-07
Infiniti Recalls M56, Q70, and Hybrid Models for Driveshaft Defect
Nissan is recalling specific Infiniti models because a broken driveshaft can cause loss of propulsion or disable the parking brake, increasing crash risk.
Product
INFINITI — INFINITI M56, Q70, M35 HYBRID, Q70 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20E089000·2020-12-07
Curt Manufacturing Recalls Securelatch Adjustable Pintle Mounts Due to Fracture Risk
Curt Manufacturing is recalling Securelatch Adjustable Pintle Mounts because the 2-inch shank may fracture while hauling, increasing the risk of a crash.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V754000·2020-12-07
2021 East to West Recreational Trailers: Stowed Grill Fire Hazard
Forest River is recalling 2021 East to West recreational trailers (approximately 115 units). The grill can be stowed with the propane hose attached and burners on, which can increase fire risk.
Product
EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V753000·2020-12-04
Mercedes-Benz A 220 Recalled for Missing Tire Pressure Labels
Mercedes-Benz is recalling 2019 A 220 vehicles because missing tire pressure labels may lead to incorrect inflation and increased crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ A 220
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V752000·2020-12-04
E-One Recalls Emergency Vehicles Due to Display Lockup Risk
E-One is recalling specific 2019-2021 emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.
Product
E-ONE — E-ONE COMMERCIAL, QUEST II, TYPHOON N, CYCLONE II
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V751000·2020-12-03
Land Rover Recalls 2020 Models for Speedometer Display Software Error
Land Rover is recalling 2020 Discovery Sport and Range Rover Evoque vehicles because a software error may cause the speedometer to randomly switch units, potentially distracting drivers.
Product
LAND ROVER — LAND ROVER RANGE ROVER EVOQUE, DISCOVERY SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21711·2020-12-03
Honda Recalls Pioneer 700 and 1000 Vehicles Due to Steering Control Issues
American Honda is recalling approximately 118,600 Pioneer 700 and 1000 vehicles because the electric power steering system may lose control, posing crash and injury hazards.
Product
Honda Pioneer 700 & 1000 Recreational Off-Highway Vehicles (ROVs) with Electric Power Steering (EPS)
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0497-2021·2020-12-02
Flexicare ProVu Video Stylet Recalled for Potential Airway Occlusion
Flexicare Medical Ltd. is recalling ProVu Single Use Video Stylets with ET Tubes because over-inflated cuffs may block the airway, making it difficult to ventilate patients.
Product
ProVu Single Use Video Stylet with ET Tube, Part/Size: 038-990-080U/ 8.0, 038-990-075U/ 7.5, 038-990-070U/ 7.0, 038-990-065U/ 6.5 *Note: product list updated per 12/23/2020 letter to customers
Category
Medical Device
Distribution
Distributed nationwide