State

Kansas product recalls

20,322 recalls have nationwide distribution and so reach Kansas. 0 additional recalls listed Kansas specifically in their distribution scope.

About recalls in Kansas

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Kansas consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

11701–11725 of 20322

SevereFDA (Devices)·Z-2510-2023·2023-09-20
Abbott Infinity 5 Implantable Pulse Generator Patients Unable to Exit MRI Mode
Some Abbott Infinity 5 implantable pulse generator patients report being unable to exit MRI mode on their devices. This Class I recall affects 5,932 devices distributed globally.
Product
Infinity 5 Implantable Pulse Generator REF 6660 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery within
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2514-2023·2023-09-20
FDA Recalls Medline Hudson RCI Addipak Inhalation Solution for Sterility Failure
Medline Industries is recalling HUDSON RCI Addipak 5mL sterile saline inhalation solution due to sterility failure. Approximately 18,000 units were distributed nationwide; the product was intended for scrap but was inadvertently shipped to customers.
Product
HUDSON RCI Addipak, UNIT DOSE VIALS, 5mL Sterile 0.9% NaCl Solution for Inhalation USP. REF RHUD59U
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2507-2023·2023-09-20
Abbott Proclaim Plus 5 Implantable Pulse Generator MRI Mode Exit Failure
Abbott Medical is recalling Proclaim Plus 5 Implantable Pulse Generators (Model 3670) due to reports that patients are unable to exit MRI mode on the devices.
Product
Proclaim Plus 5 Implantable Pulse Generator REF 3670 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery w
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2506-2023·2023-09-20
Proclaim XR 7 Implantable Pulse Generators unable to exit MRI mode
Abbott Medical is recalling Proclaim XR 7 Implantable Pulse Generators due to a malfunction that prevents patients from exiting MRI (Magnetic Resonance Imaging) mode, potentially disrupting normal device operation and therapy delivery.
Product
Proclaim" XR 7 Implantable Pulse Generator REF 3662 (previously known as Proclaim" 7 Elite IPG) Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It i
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2508-2023·2023-09-20
Proclaim Plus 7 Implantable Pulse Generator Cannot Exit MRI Mode
Abbott Medical recalled Proclaim Plus 7 Implantable Pulse Generators due to a defect preventing patients from exiting MRI mode. This operational failure could compromise device functionality during or after magnetic resonance imaging procedures.
Product
Proclaim Plus 7 Implantable Pulse Generator REF 3672 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery w
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2505-2023·2023-09-20
Proclaim XR 5 Implantable Pulse Generators Cannot Exit MRI Mode
Abbott Medical recalled the Proclaim XR 5 Implantable Pulse Generator after patients reported being unable to exit MRI mode on their devices. Approximately 113,784 units were distributed worldwide.
Product
Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1180-2023·2023-09-20
WEFUN Capsules Recalled: Unapproved Drug with Undisclosed Sildenafil
WEFUN Capsules 825 mg are being recalled due to contamination with sildenafil, an undisclosed active pharmaceutical ingredient not approved for the product. Distribution was nationwide.
Product
WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2511-2023·2023-09-20
Infinity 7 Implantable Pulse Generator Recall Due to MRI Mode Exit Failure
Abbott Medical recalls Infinity 7 Implantable Pulse Generators due to reports that patients cannot exit MRI mode. The FDA has classified this as a Class I recall affecting devices distributed worldwide.
Product
Infinity 7 Implantable Pulse Generator REF 6662 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery within
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1506-2023·2023-09-20
Mixed Vegetables Recalled for Potential Listeria monocytogenes Contamination
Twin City Foods is recalling mixed vegetable products sold under TopValu, Food Lion, and Kroger brands due to potential Listeria monocytogenes contamination. Products were distributed in the US and internationally.
Product
Mixed Vegetables BEST PRICE TOPVALU, net per bag 500g. Label is in foreign language. 4549414484120 Food Lion Mixed Vegetables Carrots, Corn, Green Beans & Peas. Product of USA, net wt. per bag 16oz, 12 bags per case. Distributed by Food Lion, LLC Salisbury, NC. UPC 35826005090
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2582-2023·2023-09-20
ACUSON Redwood 2.0 Ultrasound Systems Display Incorrect Measurement Results
ACUSON Redwood 2.0 ultrasound systems may display underestimated measurement results when using an 18L6 transducer in Dual format, potentially leading to patient misdiagnosis. 796 units are affected worldwide.
Product
ACUSON Redwood 2.0 ultrasound systems, REF: 11503314
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1503-2023·2023-09-20
Twin City Foods Frozen Corn Recalled Nationwide for Listeria Risk
Twin City Foods recalled frozen corn products due to potential Listeria monocytogenes contamination. Products distributed nationwide and internationally.
Product
Individually Quick Frozen (IQF) Corn distributed in BULK TOTES (1650lbs and 1750lbs) to consignees for further processing. Bulk tote labels have cooking instructions. Individually Quick Frozen (IQF) Super Sweet Corn, foodservice item, packaged in 32oz. plastic bag, 12 bags per
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2578-2023·2023-09-20
Medical Device Recall: ACL TOP Coagulation Analyzers for Sample Misidentification
Instrumentation Laboratory is recalling ACL TOP coagulation analyzers due to potential sample misidentification that could result in incorrect test results and alter patient management decisions.
Product
ACL TOP Family 50 Series Models as follows: In vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis (1) ACL TOP 550 CTS Model N
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2577-2023·2023-09-20
BeamAdjust software generates incorrect calibration files for radiation detectors
BeamAdjust software Version 2.3.3 generates incorrect calibration files when using TIFF or DICOM image reference data, affecting radiation measurement accuracy in OCTAVIUS Detector systems.
Product
BeamAdjust software Version 2.3.3 Ref: S080032 The following devices are affected when a relative calibration is performed using ArrayCal (module from BeamAdjust S080032, UDI-DI: EPTWS0800320 ): " OCTAVIUS Detector 1600 SRS (T10056) (UDI-DI: EPTWT100560) " OCTAVIUS Detector
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2531-2023·2023-09-20
Remel Todd Hewitt Broth Culture Medium May Fail to Detect Target Organism
One lot of Remel Todd Hewitt Broth culture medium may fail to recover Group B Streptococci during testing or use with patient samples, potentially resulting in missed diagnoses.
Product
remel TODD HEWITT W. CNA (LIM BROTH), REF R064810; used to isolate Group B Streptococci form clinical specimens containing mixed bacterial flora
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1516-2023·2023-09-20
Knorr Alphabet Pasta Soup Recalled for Undeclared Egg Allergen
Knorr Letras con Tomate soup mix is being recalled because it contains undeclared egg. Consumers with egg allergies should not consume this product.
Product
Knorr Letras con Tomate Tomato Based Alphabet Pasta Soup Mix 3.5 oz UPC: 048001716186
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1148-2023·2023-09-20
Pantoprazole Sodium for Injection Recalled Due to Sterility Concern
BE Pharmaceuticals is recalling Pantoprazole Sodium for Injection nationwide due to lack of sterility assurance caused by powder discoloration and small cracks in some vials. No illnesses have been reported.
Product
PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1504-2023·2023-09-20
Frozen Corn Recalled Due to Listeria monocytogenes Contamination
Twin City Foods frozen corn in bulk cases is recalled nationwide due to potential Listeria monocytogenes contamination. Products were distributed to food processors in the United States, Costa Rica, China, and Japan.
Product
Individually Quick Frozen (IQF) Corn, distributed in bulk cases (1kg, 10kg, 12kg, 15kg, 25kg) to consignees for further processing. Cases are read in parts: Product of U.S.A. Packed By Twin City Foods, Inc. Stanwood, Washington. Super Sweet Grade A Cut Corn Blanched Vegetables,
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1149-2023·2023-09-20
Prescription Drug Sucralfate Suspension Recalled for Out-of-Specification Potency
VistaPharm LLC is recalling Sucralfate Oral Suspension 1g/10mL due to out-of-specification assay results. The active ingredient concentration does not meet FDA specifications in approximately 14,400 affected bottles distributed nationwide.
Product
SUCRALFATE — SUCRALFATE (SUCRALFATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1514-2023·2023-09-20
Knorr Pasta Soup Mix recalled for undeclared egg allergen
Conopco (Unilever) recalled Knorr Estrellitas con Tomate soup mix nationwide due to undeclared egg allergen. No illnesses have been reported.
Product
Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mix 3.5 oz UPC: 048001716193
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1515-2023·2023-09-20
Knorr Soup Mix Recalled for Undeclared Egg Allergen
Conopco is recalling Knorr Fideos con Tomate Tomato Based Pasta Soup Mix because it contains undeclared egg. The product was distributed nationwide with best-by dates through July 6, 2024.
Product
Knorr Fideos con Tomate Tomato Based Pasta Soup Mix 3.5 oz UPC: 048001716162
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2524-2023·2023-09-20
Medtronic Bone Graft Recalled Due to Incorrect Size Labeling
Medtronic Sofamor Danek USA Inc is recalling Magnifuse Bone Graft products due to incorrect size labeling on 55 pouches. Units with specific serial numbers were distributed in nine U.S. states.
Product
Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1505-2023·2023-09-20
Twin City Foods Frozen Corn Recalled for Listeria Contamination Risk
Multiple frozen corn products distributed nationwide are being recalled due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.
Product
Kernel Corn, BEST PRICE TOPVALU, net wt. per bag 300g. Label is in foreign language. UPC 4549414086232 Signature Select Golden Corn Super Sweet, Product of USA, net wt. per bag 12oz, 12 bags per case. UPC 21130090655 Food Lion Super Sweet Cut Yellow Corn, Product of USA, net wt
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2579-2023·2023-09-20
Copaliner Cavity Varnish Recalled for Solvent Mislabeling Error
Keystone Industries recalls Copaliner Cavity Varnish after discovering bottles of Copaliner Solvent were accidentally packaged in boxes labeled as varnish. The error affected 337 units distributed worldwide.
Product
Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to provide a marginal seal between the dentin and amalgam which helps to protect against penetration of amalgam into the dentina Item No. 0921526
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2576-2023·2023-09-20
Microbiologics KWIK-STIK ANA quality control set missing strain
Microbiologics Inc is recalling one lot of KWIK-STIK ANA QC sets missing one of three bacterial strains required for microbiological testing.
Product
KWIK-STIK, ANA (3 Strains) QC Set, REF 5065P; Microbiological testing
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2580-2023·2023-09-20
Denture relining kit recalled for outer box labeling error
Keystone Industries is recalling 240 units of Henry Schein Hard Line Chairside Reline kits because the outer box is labeled as Soft Line, though the contents and instructions are correctly labeled.
Product
Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture Relining Material KI Item No.: 0921940HS Henry Schein Item No.: 570-0718
Category
Medical Device
Distribution
Distributed nationwide