State

Kansas product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37876–37900 of 79562

HighFDA (Devices)·Z-0868-2019·2019-03-06
Zimmer Biomet Recalls Vitality Spinal Fixation Set Screws
Zimmer Biomet Spine Inc. is recalling Vitality Shear-off Set Screws because a manufacturing issue prevents them from threading properly with mating components.
Product
Vitality¿ Spinal Fixation System.Spinal Intervertebral Body, Appliance, Fixation (non-sterile). Pedicle screw fixation is indicated for skeletally mature patients and for adolescent patients. For use in Orthopedic medical specialty area. Product Usage: The Vitality Shear-off…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0866-2019·2019-03-06
Zimmer Biomet Recalls Vitality Spinal Fixation Set Screws
Zimmer Biomet is recalling Vitality Shear-off Set Screws because they do not thread properly with mating components due to a manufacturing issue.
Product
Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is indicated for skeletally mature patients and for adolescent patients. For use in Orthopedic medical specialty area. Product Usage: The Vitality Shear-off Set Screw…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0869-2019·2019-03-06
Philips Prodiva CS MRI System Recalled for Falling Speaker Hazard
Philips is recalling Prodiva CS MRI systems because ceiling speakers may fall due to the magnetic field.
Product
Prodiva CS, Model Number 781069. Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0940-2019·2019-03-06
Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Leaks
Arrow International is recalling 38 units of the Arrow AutoFuser Disposable Pain Control Pump due to possible cracks that may cause leaks and reduced drug delivery.
Product
AF w/AS 550 x 1-14ML/HR CPNB, Product code MVBXL- CPNB, Arrow AutoFuser Disposable Pain Control Pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0871-2019·2019-03-06
Philips Multiva MRI System Recalled for Falling Ceiling Speaker Hazard
Philips is recalling Multiva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Product
Multiva 1.5T 8 R5 (ZBO), Model Number 781072. Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0883-2019·2019-03-06
Philips Intera 3.0T MRI System Recalled for Ceiling Speaker Hazard
Philips is recalling Intera 3.0T MRI systems because ceiling speakers may fall due to magnetic attraction.
Product
Intera 3.0T Master/Quasar Dual, Model Number 781150. Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0941-2019·2019-03-06
Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks
Arrow International Inc. is recalling Arrow AutoFuser Disposable Pain Control Pumps due to possible cracks on the fill port connector that may cause leaks and reduced drug delivery.
Product
AF w/AS 550x 0.5 7 ml/hr, 5ml 30 LO CPNB, Product code MVAX30XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0956-2019·2019-03-06
Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Leaks
Arrow International Inc. is recalling Arrow AutoFuser Disposable Pain Control Pumps due to possible cracks on the fill port connector that may cause leaks and reduced drug delivery.
Product
AF w/AS 550 x 1-14ML/HR 5ML-60LO CPNB, Product code MVBX60XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0898-2019·2019-03-06
Philips Panorama 1.0T MRI System Recalled for Ceiling Speaker Hazard
Philips is recalling Panorama 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Product
Panorama 1.0T, Model Number 781250. Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0942-2019·2019-03-06
Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks
Arrow International Inc. is recalling 8 units of the Arrow AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.
Product
AF550x5ML/H 2ML 60LO 6" CATH, 4.5" IN, Product code MT5060XLSK5 CP, Arrow AutoFuser Disposable Pain Control Pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0939-2019·2019-03-06
Merge Eye Station Retinal Imager Recalled for Electrical Safety Defects
Merge Healthcare is recalling 1,252 WinStation Retinal Imagers because certain configurations may produce electrical output exceeding allowable medical device limits.
Product
The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product Usage: The WinStation Retinal Imager has the same intended use as other fundus cameras. It is specifically used to produce color or black and white images of the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0949-2019·2019-03-06
Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks
Arrow International Inc. is recalling 9 units of the Arrow AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.
Product
AF 550 x 5ML/HR CPNB, Product code MC0050XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0872-2019·2019-03-06
Philips Multiva MRI System Recalled for Ceiling Speaker Hazard
Philips is recalling Multiva 1.5T MRI systems because ceiling speakers may fall due to magnetic attraction.
Product
Multiva 1.5T 16 R5 (ZBO), Model Number 781073. Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0887-2019·2019-03-06
Philips MRI System Recall for Falling Ceiling Speaker Hazard
Philips is recalling Intera Achieva 1.5T Pulsar MRI systems because ceiling speakers may fall due to magnetic attraction.
Product
Intera Achieva 1.5T Pulsar, Model Number 781171. Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0961-2019·2019-03-06
Alcon Ophthalmic Microscope Recalled for Potential Optical Head Detachment
Alcon is recalling LuxOr E71 and E71 Q-Vue ophthalmic microscopes because the optical head may detach from the stand due to missing thread adhesive.
Product
Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic surgical procedures for cataract, retina and cornea.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0925-2019·2019-03-06
Philips MR-OR 3.0T MRI Systems Recalled for Falling Speaker Hazard
Philips is recalling 11,226 MR-OR 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Product
MR-OR 3.0T, Model Number 781438. Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0899-2019·2019-03-06
Philips Achieva XR MRI Systems Recalled for Falling Speaker Hazard
Philips is recalling Achieva XR MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Product
Achieva XR 1.5T/3.0T , Model Number 781253. Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0909-2019·2019-03-06
Philips Achieva MRI Systems Recalled Due to Ceiling Speaker Hazard
Philips is recalling 11,226 Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Product
Achieva 1.5T, Model Number 781296. Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1102-2019·2019-03-06
Citrus Systems Recalls Nature's Nectar Orange Juice for Pasteurization Failure
Citrus Systems Inc is recalling Nature's Nectar High Pulp Orange Juice because the product cannot be verified as having achieved the required 5-log reduction per 21 CFR 120.
Product
Nature's Nectar High Pulp Orange Juice, Never from Concentrate. Item # 420025. Pasteurized. Net 52 FL OZ (1.6 QT) 1.53L. Kosher. UPC 4 099100 056907. Keep Refrigerated. Distributed by Aldi, Inc. Batavia, IL 60510.
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-1097-2019·2019-03-06
Planetary Herbals Mullein Lung Complex Recalled for Labeling Error
Planetary Herbals is recalling Mullein Lung Complex capsules due to a labeling error regarding inactive ingredients.
Product
Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF0003; 90 count - Item number PF0002; 180 count, Item number PF0106 and 90 + 90 count, PF 7013 white plastic bottles. Proprietary Blend: Platycodon root, Ophiopagon Rhizome, Long Pepper Fruit, Black…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0933-2019·2019-03-06
Becton Dickinson Recalls Phoenix AST-s Indicator Due to Test Aborts
Becton Dickinson is recalling Phoenix AST-s Indicator lots because they cause increased test aborts. The products were distributed to 41 US states and 33 foreign countries.
Product
Phoenix AST-s Indicator, Catalog Number 246009
Category
Medical Device
Distribution
42 states
ModerateFDA (Devices)·Z-0967-2019·2019-03-06
Cook Inc. Recalls Gastrointestinal Suture Anchor Sets Due to Retention Mechanism Issue
Cook Inc. is recalling 797 Entuit Secure Gastrointestinal Suture Anchor Sets because a specific extension spring lot may cause difficulty sliding the retention mechanism.
Product
Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-2, Order Number G35569 The Entuit Secure Gastrointestinal Suture Anchor Set is intended for anchoring the anterior wall of the stomach to the abdominal wall prior to the introduction of interventional…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0959-2019·2019-03-06
Shimadzu BRANSIST safire Digital Angiography System Software Recall
Shimadzu Medical Systems is recalling eight BRANSIST safire digital angiography systems due to a software error that can cause abnormal termination during initial patient registration.
Product
BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is intended to be used for radiologic visualization of the heart, blood vessels or lymphatic system during or after injection of a contrast medium. It is to be used in the diagnosis of the circulatory…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0968-2019·2019-03-06
Cook Inc. Recalls Gastrointestinal Suture Anchor Sets Due to Retention Mechanism Issue
Cook Inc. is recalling 975 Entuit Secure Gastrointestinal Suture Anchor Sets because a specific extension spring lot may cause difficulty sliding down the retention mechanism.
Product
Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-3, Order Number G35570 The Entuit Secure Gastrointestinal Suture Anchor Set is intended for anchoring the anterior wall of the stomach to the abdominal wall prior to the introduction of interventional…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0935-2019·2019-03-06
Becton Dickinson Recalls Phoenix AP AST Indicator Bags Due to Test Aborts
Becton Dickinson is recalling Phoenix AP AST Indicator Bags because certain lots cause increased test aborts. The products were distributed to 40 US states and 33 foreign countries.
Product
Phoenix AP AST Indicator Bag, Catalog Number 246006
Category
Medical Device
Distribution
42 states