State

Kansas product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50576–50600 of 79649

HighFDA (Devices)·Z-2848-2016·2016-09-28
Smith & Nephew Recalls Renasys Sterile Transparent Film Due to Seal Failures
Smith & Nephew is recalling Renasys Sterile Transparent Film and related dressing kits because sterility seal integrity failures may compromise the sterile barrier.
Product
RENASYS Sterile Transparent Film and all the RENASYS Dressing kits that contains the RENASYS Sterile Transparent Film Is intended for patients who would benefit from a suction device (negative pressure) to help promote wound healing by removing fluids including irrigation and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2849-2016·2016-09-28
TriMed Recalls Semi-Tubular Plates Due to Screw Failure During Implantation
Trimed Inc is recalling 30 units of SMTP-10 Semi-Tubular Plates because a non-locking screw passed through a plate hole during implantation.
Product
TriMed Semi-Tubular Plate, 10-Hole, Model No. SMTP-10 Contoured plate with offset screw holes. The plate is 103 mm in length, 1.3 mm thick and 9.6 mm wide. The part is made of surgical steel conformance with ASTM F138 or F139. The plate is used to fixation of long bone…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2871-2016·2016-09-28
Merge Healthcare Recalls CADstream MRI Software Due to Grid Selection Error
Merge Healthcare is recalling CADstream software versions 4.1.3 and prior because an incorrect grid selection could lead to an incorrect biopsy or missed target during MRI analysis.
Product
CADstream software. Product Usage: CADstream is an image processing system designed to assist in the visualization, analysis, and reporting of magnetic resonance imaging (MRI) studies. CADstream also is intended to provide workflow efficiency and interventional planning…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V699000·2016-09-28
Newmar Recalls Canyon Star RVs Due to Wheelchair Door Defect
Newmar is recalling 2015-2017 Canyon Star recreational vehicles because the wheelchair access door may open while driving, increasing crash risk.
Product
NEWMAR — NEWMAR CANYON STAR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-2333-2016·2016-09-28
Immune Tree Recalls Colostrum Powder Due to Undeclared Milk Allergen
Immune Tree is recalling specific colostrum powder products because they contain undeclared milk, a major food allergen.
Product
Colostrum6 Powder (6.5 oz) Item No. 9902; Sold under the following brands: Immune Tree, Surthrival, HealthWorks (Not purchased since 3/18/15). Packaged in HDPE White bottle, except Surthrival which uses a Brown HDPE Bottle
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2335-2016·2016-09-28
Immune Tree Recalls Colostrum Powder Due to Undeclared Milk Allergen
Immune Tree is recalling specific colostrum powder products because they contain undeclared milk, a major food allergen.
Product
Colostrum6 Powder Kilo (35.3 oz); Item No. 9903; Brand Name Immune Tree, Surthrival, Packaged using HDPE White bottle, except Surthrival which uses a Brown HDPE Bottle
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2866-2016·2016-09-28
Sorin S5 Heart-Lung Machine Recalled for Power Supply Failure Risk
Sorin Group USA is recalling 5,264 Stöckert S5 Heart-Lung Machines worldwide due to a potential failure of the Uninterruptible Power Supply.
Product
St¿ckert S5 System, S5 Heart-lung machine, Cardiopulmonary bypass heart-lung machine console Product Usage: The St¿ckert S5 System is intended to be used during cardiopulmonary bypass for procedures lasting six (6) hours or less. These devices come in direct contact with the…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V698000·2016-09-28
Ford Recalls 2013-2017 Focus Hatchbacks for Latch Defect
Ford is recalling 2013-2017 Focus hatchbacks with manual transmissions because the rear hatch may unlatch with a single button press, increasing injury risk.
Product
FORD — FORD FOCUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2842-2016·2016-09-28
Philips HeartStart MRx Monitor/Defibrillator Recall for Handle Separation
Philips is recalling 394 HeartStart MRx Monitor/Defibrillators because the handle can separate from the housing due to broken mounts.
Product
HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2084-2016·2016-09-28
Campbell's SpaghettiOs Recalled for Potential Choking Hazard from Plastic Pieces
Campbell Soup Supply Co. is recalling 14,789 cases of SpaghettiOs due to a potential choking hazard from red plastic pieces found in the cans.
Product
Campbell's SpaghettiOs Original Pasta in Tomato and Cheese Sauce Net Wt. 14.2 ounces in metal cans, NDC: 0-51000-22432-3
Category
Food
Distribution
15 states
HighFDA (Food)·F-2330-2016·2016-09-28
Southern Grove Cashews Recalled for Possible Peanut Presence
Kanan Enterprises is recalling Southern Grove Cashews with Sea Salt due to the possible presence of peanuts. The product was distributed in Ohio, Kansas, and Minnesota.
Product
Southern Grove Cashews with Sea Salt, a 10 ounce stand up pouch bag with a UPC 0 38445 12286 5 and the date codes of Best By May 24 2017 KN and August 05 2017 KN
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2336-2016·2016-09-28
Immune Tree Recalls Colostrum Powder Due to Undeclared Milk Allergen
Immune Tree is recalling specific colostrum powder products because they contain undeclared milk, a major food allergen.
Product
Colostrum6 Powder (2.5 oz), Item No. 9915, Sold under brand Immune Tree (discontinued), Packaged using HDPE White bottle
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2855-2016·2016-09-28
Abbott Recalls SENSAR Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling 84 SENSAR Foldable Intraocular Lenses because they were not checked prior to release, which may result in the release of mislabeled units.
Product
SENSAR Foldable IOL with OptiEdge Design, Model No. AR40e The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2867-2016·2016-09-28
Invivo Recalls Philips Expression IP5 MRI Patient Monitoring Units
Invivo Corporation is recalling 639 Philips Expression Information Portal (IP5) units because display numerics may freeze and menu keys may disable after extended run time.
Product
Philips Expression Information Portal (IP5) Model 865471. The IP5 is intended to be used as a secondary display control unit for the Expression MRI Patient Monitoring System and the Expression MR200 MRI Patient Monitoring System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2872-2016·2016-09-28
McKesson Radiology Software Recalled for Missing STAT Priority Icon
McKesson Medical Imaging Group is recalling McKesson Radiology software versions 12.1.1 and 12.2 because the STAT priority icon was not displayed in the Study List when a study was opened.
Product
McKesson Radiology, versions 12.1.1 and 12.2 McKesson Radiology (MR) is a Picture Archiving Communication System (PACS). It is a medical image and information management application that is intended to receive, transmit, store, retrieve, display, print and process digital…
Category
Medical Device
Distribution
40 states
ModerateFDA (Devices)·Z-2859-2016·2016-09-28
Abbott Recalls Intraocular Lenses Due to Mislabeled Product Release
Abbott Medical Optics is recalling 131 TECNIS OptiBlue intraocular lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS OptiBlue 1-Piece Intraocular Lens (IOL), Model No. ZCB00V The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2857-2016·2016-09-28
Abbott Recalls TECNIS Symfony Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling 10 TECNIS Symfony intraocular lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS Symfony Extended Range of Vision IOL, Model No. ZXR00 The product is indicated primary implantation for the visual correction of aphakia in adult patients with and without presbyopia in whom a cataractous lens has been removed by extracapsular cataract extraction, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1504-2016·2016-09-28
Sun Pharmaceutical Recalls Carvediol Tablets Due to Impurity Failures
Sun Pharmaceutical Industries is recalling specific lots of Carvediol Tablets because they failed impurity and degradation specifications.
Product
Carvediol Tablets , USP, 3.125 mg, 100-count bottle (NDC 57664-242-88). 500-count bottle (NDC 57664-242-13), 1000-count bottle (NDC 57664-242-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by Sun…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2860-2016·2016-09-28
Abbott Recalls SENSAR Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling SENSAR 1-Piece Intraocular Lenses because they were not checked prior to release, which may result in the release of mislabeled units.
Product
SENSAR 1-Piece IOL, Model No. AAB00 The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2852-2016·2016-09-28
Siemens Syngo.x Software Recalled for Incorrect Volume Calculations
Siemens Medical Solutions is recalling 338 Syngo.x PACS systems because a software error caused volume calculations for prostate and liver to be too high.
Product
Syngo.x picture archiving and communication system Syngo.x is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2862-2016·2016-09-28
Abbott Recalls Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling 70 units of TECNIS OptiBlue Intraocular Lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS OptiBlue 1-Piece IOL with the TECNIS iTec Preloaded Delivery System, Model No. PCB00V The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1507-2016·2016-09-28
Sun Pharmaceutical Recalls Carvediol Tablets Due to Impurity Failures
Sun Pharmaceutical Industries is recalling Carvediol Tablets, USP, 25 mg, because the product failed impurities and degradation specifications.
Product
Carvediol Tablets, USP, 25 mg, 100-count bottle (NDC 57664-247-88), 500-count bottle (NDC 57664-247-13), 1000-count bottle (NDC 57664-247-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by: Sun Pharmaceutical…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2856-2016·2016-09-28
Abbott Recalls TECNIS Multifocal Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling 77 TECNIS Multifocal Intraocular Lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS Multifocal 1-Piece Intraocular Lens, Model No. ZKB00, ZLB00; The product is indicated for primary implantation for the visual correction of aphakia in adult patients with and without presbyopia in whom a cataractous lens has been removed by extracapsular cataract…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2869-2016·2016-09-28
Hologic Sertera Biopsy Device Recalled for Incorrect Labeling
Hologic is recalling 570 units of the Sertera Biopsy Device due to incorrect labeling on the sterile kit.
Product
Sertera Biopsy Device, Sterile; Used primarily in ultrasound-guided breast biopsies.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2853-2016·2016-09-28
Siemens Syngo.via Software Recalled for Incorrect Volume Calculations
Siemens Medical Solutions is recalling 338 Syngo.via systems because a software error caused volume calculations for prostate and liver to be too high.
Product
Syngo.via picture archiving and communication system Syngo via is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images.
Category
Medical Device
Distribution
Distributed nationwide