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.

48576–48600 of 79646

ModerateFDA (Devices)·Z-0965-2017·2017-01-18
ASP Recalls EVOTECH Endoscope Cleaner Due to Hose Leak Risk
Advanced Sterilization Products is recalling 107 EVOTECH Endoscope Cleaner and Reprocessor Systems because a hose may come loose and cause a leak.
Product
EVOTECH Endoscope Cleaner and Reprocessor System 208V, Product Code: 50004 The EVOTECH ECR Endoscope Cleaner and Reprocessor, a washer/disinfector, is indicated for use with high-level disinfectant CIDEX OPA Concentrate Solution and an enzymatic detergent (CIDEZYME XTRA) to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1017-2017·2017-01-18
Merge Eye Station Software Recalled for Potential Data Deletion
Merge Healthcare is recalling Merge Eye Station software versions 11.6.0 and prior due to a risk of accidental patient record deletion.
Product
Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager distributed by Ophthalmic Imaging Systems (OIS). Versions: 11.6.0 and prior
Category
Medical Device
Distribution
52 states
ModerateFDA (Devices)·Z-1002-2017·2017-01-18
Siemens Biograph mCT Flow 40-4R Laser Cover Window Recall
Siemens Medical Solutions is recalling Biograph mCT Flow 40-4R scanners because laser cover windows may fall off.
Product
Biograph mCT Flow 40-4R, Material Number 10529159 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0957-2017·2017-01-18
Straumann Dental Implant Drills Recalled for Tolerance Specification Failures
Straumann Manufacturing is recalling 165 dental implant drills because they cannot be inserted into handpieces due to tolerance specification failures.
Product
Straumann Drill 1, short, ¿ 2.2mm, l 33.0mm, SS-Non sterile. Dental implant accessory Article Number: 044.210 Dental implants drill accessory is intended to prepare osteotomy site for surgical dental implant placement. Dental implants are intended for immediate placement…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0979-2017·2017-01-18
Siemens Recalls Intact PTH Assay Kits Due to Negative Bias
Siemens is recalling IMMULITE 2000 Intact PTH assay kits because they may show a negative bias of up to -39% at low concentrations.
Product
SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test Code iPTH, REF/Catalog Number L2KPP2, Siemens Material Number (SMN) 10381441 and REF/Catalog Number L2KPP6, SMN 10381442; IVD --- Made in UK -- Siemens healthcare Diagnostics Products Ltd. Glyn…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0975-2017·2017-01-18
GE OEC Mobile Fluoroscopy Systems Recalled for Power Cable Failures
GE Healthcare is recalling OEC 9900 Elite and other mobile fluoroscopy systems because the workstation power cable assembly can fail intermittently.
Product
The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedure. Examples of clinical application may include cholangiography, endoscopy, urologic, orthopedic…
Category
Medical Device
Distribution
50 states
ModerateFDA (Devices)·Z-1001-2017·2017-01-18
Siemens Biograph mCT Flow Edge-4R Scanner Recall for Laser Cover Windows
Siemens Medical Solutions is recalling one Biograph mCT Flow Edge-4R scanner because laser cover windows may fall off.
Product
Biograph mCT Flow Edge-4R, Material Number 10528955 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0999-2017·2017-01-18
Siemens Biograph mCT-X Scanner Recall Due to Falling Laser Cover Windows
Siemens Medical Solutions is recalling Biograph mCT-X scanners because laser cover windows may fall off.
Product
Biograph mCT-X w/TrueV Upgrade, Material Number 10250745 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0995-2017·2017-01-18
Siemens Biograph mCT Scanners Recalled for Falling Laser Cover Windows
Siemens Medical Solutions is recalling 88 Biograph mCT scanners because laser cover windows may fall off.
Product
Biograph mCT S(40)-4R, Material Number 10248671 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0958-2017·2017-01-18
Straumann Twist Drill PRO Recalled for Tolerance Specification Defects
Straumann Manufacturing is recalling 120 units of Twist Drill PRO dental implant accessories because they cannot be inserted into handpieces due to tolerance specification failures.
Product
Straumann Twist Drill PRO ¿4.2mm,long,41mm,SS-Non sterile. Dental implant accessory Article Number: 044.255 Dental implants drill accessory is intended to prepare osteotomy site for surgical dental implant placement. Dental implants are intended for immediate placement and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0960-2017·2017-01-18
Trilliant Tiger Screw Sterilization Tray Base Assembly Recall for Printing Error
Trilliant Surgical Ltd. is recalling Tiger Screw Sterilization Tray Base Assemblies due to a printing error on k-wire description markings.
Product
Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N, O The product is a component of a system indicated for the fixation of fractures, non-unions, arthrodeses, and osteotomies of bones appropriate for the size of the device.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0993-2017·2017-01-18
Siemens Biograph mCT Scanners Recalled for Falling Laser Cover Windows
Siemens is recalling 34 Biograph mCT scanners because laser cover windows may fall off, posing a potential hazard to users.
Product
Biograph mCT S(64)-3R, Material Number 10248669 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0981-2017·2017-01-18
Bard Access Systems Recalls StatLock PICC Plus Devices Due to Missing Identifiers
Bard Access Systems is recalling StatLock PICC Plus Crescent Foam devices because some pouches lack unique product identifiers like lot numbers.
Product
StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Packaged as a single unit with a skin protectant pad and foam strips in a Tyvek pouch. Depending on configuration, there are either 25 or 50 pouches per carton and 10 cartons per case. Other configurations may…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0974-2017·2017-01-18
GE OEC MiniView 6800 C-Arm Recalled for Power Cable Failures
GE Healthcare is conducting a voluntary field action for OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 devices due to intermittent power cord failures.
Product
OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 6800 Digital Mobile C-Arm is designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imaging. The device is not intended for…
Category
Medical Device
Distribution
50 states
ModerateFDA (Devices)·Z-0982-2017·2017-01-18
Bard Access Systems Recalls StatLock Catheter Stabilization Devices
Bard Access Systems is voluntarily recalling StatLock CV Plus catheter stabilization devices because some pouches lack unique product identifiers.
Product
StatLock¿ CV Plus w/Pigtail. Product Code: CV0220CE & CV0220. Packaged as a single unit with a skin protectant pad and foam strips in a Tyvek pouch. Depending on configuration, there are either 25 or 50 pouches per carton and 10 cartons per case. Other configurations may contain…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0971-2017·2017-01-18
Siemens Artis zee/zeego Angiographic X-ray System Recall for Generator Defects
Siemens is recalling Artis zee/zeego angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.
Product
Artis zee/zeego, Angiographic x-ray system Stand alone system The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0985-2017·2017-01-18
Bard Access Systems Recalls MiniLoc Safety Infusion Sets Due to Labeling Errors
Bard Access Systems is recalling MiniLoc Safety Infusion Sets because some units have needle lengths and gauges that differ from the label descriptions.
Product
MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code: S02022-75. Packaged as single units in thermoformed trays. There are 20 MiniLoc¿ trays per case and 160 per carton. Product Usage: Intended for the administration of fluids and drugs, or blood…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1016-2017·2017-01-18
Hospira Recalls Minibore Extension Sets Due to Solvent Occlusion
Hospira is voluntarily recalling one lot of Minibore Extension Sets due to a confirmed report of solvent occlusion that may prevent priming and delay therapy.
Product
Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the administration of drugs and solutions to a patient's vascular system through a vascular access device.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0998-2017·2017-01-18
Siemens Biograph mCT PET/CT Scanner Laser Cover Window Recall
Siemens Medical Solutions is recalling Biograph mCT PET/CT scanners because laser cover windows may fall off.
Product
Bio mCT-S(40) 3R->4R Upgrade, Material Number 10250743 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0973-2017·2017-01-18
GE Healthcare Recalls OEC 9800 Imaging Systems Due to Power Cable Failures
GE Healthcare is conducting a voluntary field action for OEC 9800 systems because the workstation power cable assembly can cause intermittent power cord failures.
Product
OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscopy, urologic, orthopedic…
Category
Medical Device
Distribution
50 states
ModerateUSDA FSIS·006-2017·2017-01-18
Burgers Ozark Country Cured Recalls Mislabeled Turkey Products
Burgers Ozark Country Cured is recalling approximately 1,905 pounds of fully cooked turkey products due to misbranding. The products contain undeclared sodium nitrite.
Product
Burger's Ozark Country Cured Hams, Inc. — Burgers Ozark Country Cured Recalls Poultry Products Due To Misbranding
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0986-2017·2017-01-18
Bard Access Systems Recalls SafeStep Huber Needle Sets Due to Labeling Errors
Bard Access Systems is recalling SafeStep Huber Needle Sets because some units may have needle lengths or gauges that differ from the label.
Product
SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN. Packaged as single units in thermoformed trays. There are 25 SafeStep¿ trays per case and 100 per carton. Product Usage: Intended for the administration of fluids and drugs, or blood sampling through…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0996-2017·2017-01-18
Siemens Biograph mCT PET/CT Scanners Recalled for Falling Laser Cover Windows
Siemens Medical Solutions is recalling 102 Biograph mCT PET/CT scanners because laser cover windows may fall off.
Product
Biograph mCT S(64)-4R, Material Number 10248672 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1000-2017·2017-01-18
Siemens Biograph mCT 20 Excel PET/CT Scanner Recall for Laser Cover Windows
Siemens is recalling 51 Biograph mCT 20 Excel scanners because laser cover windows may fall off.
Product
BIOGRAPH mCT 20 Excel, Material Number 10507786 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0955-2017·2017-01-18
VOCO Futurabond M+ adhesive recalled for labeling mix-up
Voco GmbH is recalling 50 units of VOCO Futurabond M+ adhesive due to a labeling error where the product was marked as Futurabond M+ Universal Adhesive.
Product
VOCO Futurabond M+ adhesive, RF 1515, Manufactured by VOCO GmbH, Futurabond M+ is a dental adhesive for use with methacrylate-based restorative, core build-up or luting materials. It can be applied with phosphoric acid etching (selective enamel etching or total-etch) of the…
Category
Medical Device
Distribution
Distributed nationwide